April 10, 2026 — Middletown, CT — Blueroot Health of Middletown, Connecticut is expanding its voluntary recall of its Vital Nutrients Aller-
"Company Announcement
April 10, 2026 — Middletown, CT — Blueroot Health of Middletown, Connecticut is expanding its voluntary recall of its Vital Nutrients Aller-C dietary supplements due to the potential to contain undeclared egg, hazelnut, and soy. The initial recall, which included lots 25E04-A and 25E04-B, has been expanded to include all product made from lot 25E04. People who have allergies and/or severe sensitivity to egg, hazelnut, and soy run the risk of a serious or life-threatening allergic reaction if they consume this product.
Aller-C was distributed nationwide by VitalNutrients.co and other online retailers.
The recalled product is packaged in a white plastic bottle containing 100 or 200 capsules and includes lot numbers 25E04, 25E04-A, and 25E04-B with an expiration date of 05/27 on the side of the bottle.
Vital Nutrients Aller-C, 200 count
UPC 693465524213 and
UPC 693465000090
Lot number 25E04-B
Expiration date 05/27
Vital Nutrients Aller-C, 100 count
UPC 693465524114 and
UPC 693465000083
Lot number 25E04 and
Lot number 25E04-A and
Lot number 25E04-B
Expiration date 05/27
The impacted lots were distributed from September 2025 to March 2026.
The allergens were discovered as part of routine internal testing and promptly reported by the company to the FDA. No illnesses have been reported to date in connection with this product.
Consumers who have purchased this product are asked to immediately discontinue use and return the product to Blueroot Health for a replacement product. Consumers with questions may contact Blueroot Health at (888) 328-9992 Monday through Friday 8:00am – 7:00pm, or [email protected]."
FOR IMMEDIATE RELEASE – March 19, 2026– West Sacramento, CA, Gear Isle is voluntarily recalling the following products to the consumer level
Summary: Another week, another (two) product(s) marketed as sexual enhancement that contain actual Viagra and Cialis not listed on the label. Just get a prescription, okay? So you have a little better chance of knowing if one of the meds you're on interacts with another?
"Company Announcement
FOR IMMEDIATE RELEASE – March 19, 2026– West Sacramento, CA, Gear Isle is voluntarily recalling the following products to the consumer level. The products have been found to contain undeclared active pharmaceutical ingredients, sildenafil and tadalafil.
Gold Lion Aphrodisiac Chocolate Sachet, UPC 795847916279, LOT# no lot number, Expires: 06/2027
ilum Sex Chocolate, UPC 1002448578911, LOT# no lot number, Expires: 12/25/2027.
Risk Statement: Use of products with undeclared active ingredients sildenafil and tadalafil may pose a threat to consumers because the active ingredient may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life-threatening. Among the adult male population who are most likely to use these products, adult males who use nitrates for cardiac conditions are most at risk from these products. To date, Gear Isle has not received any reports of adverse events related to this recall.
The product is labeled as a dietary supplement and is packaged as indicated [above]. The product can also be identified by using the attached images. The products were distributed nationwide via internet sales.
Gear Isle is notifying its customers by notification letter and is arranging for returns and refunds of all recalled products. Consumers who have the product(s) (see table) that are being recalled should stop using them and return them for a refund.
Consumers with questions regarding this recall can contact Gear Isle customer service by calling 888-387-4753 or emailing [email protected] on Monday to Friday from 10 am to 4 pm PST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm2 or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration."
FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan
Summary: Kian Pee Wan capsules, marketed as an appetite stimulant, have been found to contain a corticosteroid and a prescription antihistamine and are being recalled.
"Company Announcement
FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug ingredients dexamethasone and cyproheptadine. Products containing dexamethasone and cyproheptadine cannot be marketed as dietary supplements. Kian Pee Wan capsules are an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
Risk Statement: Dexamethasone is a corticosteroid commonly used to treat inflammatory conditions. Corticosteroid use can impair a person’s ability to fight infections and can cause high blood sugar levels, muscle injuries, psychiatric problems, and lead to cardiovascular events. When corticosteroids are taken for a prolonged period, or at high doses, they can suppress the adrenal gland (a disorder in which the adrenal glands do not produce enough hormones) and adverse consequences can range from limited adverse consequences to death. Additionally, abrupt discontinuation can cause withdrawal symptoms. Cyproheptadine is a prescription antihistamine used for seasonal allergy treatment. Consumption of undeclared cyproheptadine may cause sedation, dizziness, fatigue, restlessness, dry mouth, nausea, diarrhea/constipation, urinary retention, blurred vision.
Kian Pee Wan capsules are marketed as a dietary supplement for weight gain and stimulating appetite. It is packaged in a white bottle with beige label containing 30 pills. Kian Pee Wan capsules were distributed nationwide online on eBay.com.
Aphreseller (Ebay seller ID) is notifying its customers by this press announcement and via email and is arranging for returns of this recalled product. Customers and retailers that have Kian Pee Wan capsules, should stop using this product and/or return to the place of purchase, discard, or contact their doctor.
Consumers with questions regarding this recall can contact SiewLee Wong by email at [email protected] or via phone at 347-313-8605, Monday through Friday from 10am till 6pm Eastern Time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this recalled product. Customers can return their product to the point of purchase for a refund. Customers that bought from Aphreseller (Ebay seller ID) can return to 136-61 41st Ave, #602, Flushing NY 11355
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: www.fda.gov/medwatch/report.htm1
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm2 or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration."
March 27, 2026 — Middletown, CT — Blueroot Health of Middletown, Connecticut is voluntarily recalling two lots of Vital Nutrients Aller-C di
"Company Announcement
March 27, 2026 — Middletown, CT — Blueroot Health of Middletown, Connecticut is voluntarily recalling two lots of Vital Nutrients Aller-C dietary supplements due to the potential to contain undeclared egg, hazelnut, and soy. People who have allergies and/or severe sensitivity to egg, hazelnut, and soy run the risk of a serious or life-threatening allergic reaction if they consume this product.
Aller-C was distributed nationwide by VitalNutrients.coExternal Link Disclaimer and other online retailers.
The recalled product is packaged in a white plastic bottle containing 100 or 200 capsules and includes lot numbers 25E04-A and 25E04-B with an expiration date of 05/27 on the side of the bottle.
Vital Nutrients Aller-C, 200 count
UPC 693465524213 and
UPC 693465000090
Lot number 25E04-B
Expiration 05/27
Vital Nutrients Aller-C, 100 count
UPC 693465524114 and
UPC 693465000083
Lot number 25E04-A and
Lot number 25E04-B
Expiration 05/27
The allergens were discovered as part of routine internal testing and promptly reported by the company to the FDA. No illnesses have been reported to date in connection with this product.
Consumers who have purchased this product are asked to immediately discontinue use and return the product to Blueroot Health for a replacement product. Consumers with questions may contact Blueroot Health at (888) 328-9992 Monday through Friday 8:00am – 7:00pm, or [email protected]."
February 27 2026 — Albuquerque, New Mexico, Primal Supplements Group LLC is voluntarily recalling all orders of Primal Herbs Volume placed b
Summary: Yet again, a supplement marketed to solve erectile dysfunction via herbal means has been found to contain a prescription-only erectile dysfunction drug not listed on the label in it. This matters because drug interactions are a thing. This is a pattern across the genre, y'all.
"Company Announcement
This recall is being conducted in coordination with the U.S. Food and Drug Administration (FDA).
Here is a link to our voluntary recall: (link to the FDA recall article will be presented here)
FOR IMMEDIATE RELEASE - February 27 2026 — Albuquerque, New Mexico, Primal Supplements Group LLC is voluntarily recalling all orders of Primal Herbs Volume placed between July 2 and September 19, 2025, because FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
Sildenafil is the active ingredient in the FDA-approved prescription drug Viagra, used to treat erectile dysfunction. FDA approval of Viagra is restricted to use under the supervision of a licensed health care professional. This undeclared ingredient may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.
Customers who placed an order between July 2, 2025 and September 19, 2025, on the website: primalherbs.comExternal Link Disclaimer, should discontinue use immediately. The product is packaged in 8.5 oz round containers with green labels.
If your order was placed during this timeframe, please stop using the product and contact our team at [email protected] with your order number. We'll take care of you right away with your choice of a complimentary replacement shipment or full store credit, along with simple return instructions.
Updates will be posted here as needed.
For questions or concerns, please contact [email protected] or +1 (856) 420-6117. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Primal Herbs is conducting this recall voluntarily and takes this matter very seriously. We apologise for the inconvenience and concern this recall may cause our customers. Our company is committed to ensuring the quality of our products and the well-being of our consumers.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Complete and submit the report Online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178"
BROOKLYN, N.Y., Feb. 27, 2026 /PRNewswire/ -- USALESS.COM is recalling its RHINO CHOCO VIP
10X, in 10 gr, 12 pc packages that come in a bla
"Company Announcement
BROOKLYN, N.Y., Feb. 27, 2026 /PRNewswire/ -- USALESS.COM is recalling its RHINO CHOCO VIP 10X, in 10 gr, 12 pc packages that come in a black cardboard box marked with UPC Code 724087947668 on the back and with an expiration date of 10/2027 stamped on the back. The product is sold in retail stores and through on-line sites.
Rhino Choco VIP 10X contains Tadalafil, which is not listed on the product label. Tadalafil is the active ingredient in Cialis, an FDA-approved prescription drug, used to treat erectile dysfunction. The undeclared ingredient may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.
The product has been immediately removed from our online store until we are certain that the problem has been corrected.
Consumers who have purchased Rhino Choco VIP 10x from usaless.com are urged to immediately return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-872-5377 or [email protected]."
Costa Mesa, California — February 13, 2026 — Green Lumber Holding, LLC (“Green Lumber”) is issuing an updated consumer alert regarding count
Moving on to the "undisclosed" boner drug segment of the FDA's product recalls / recall updates:
"Costa Mesa, California — February 13, 2026 — Green Lumber Holding, LLC (“Green Lumber”) is issuing an updated consumer alert regarding counterfeit products falsely marketed as genuine Green Lumber products that may pose potential health risks.
This update follows the U.S. Food and Drug Administration’s (FDA) February 9 publication in its Enforcement Report referencing Green Lumber’s original recall, which was initiated on August 28, 2025. The recall was issued in late August 2025 after FDA testing detected tadalafil—an undeclared prescription drug—in products labeled as Green Lumber. Tadalafil is not an ingredient in any authentic Green Lumber product. The February 9 Enforcement Report does not announce a new recall; it reflects publication of the previously announced August 28, 2025, recall.
Following the FDA’s findings, Green Lumber conducted an internal investigation and determined that a company employee had misappropriated legitimate packaging and customer information to distribute counterfeit or adulterated products. That employee has been terminated.
How to Identify the Counterfeit Recalled Product
The counterfeit recalled product bears the Lot Number LOT308EXP03/28 – This is the only lot number being recalled and is not an authentic Green Lumber lot number and was used in connection with counterfeit products. Consumers should not use any product labeled with this lot number, and it should be discarded.
How to Identify Legitimate Green Lumber Products
Authentic Green Lumber products that are presently being distributed bear the following lot numbers and are not the subject of the recall:
LOTGL0130151EXP0926
GL01EXP09/27
LOT GL110725 EXP110727
Packaging differences are illustrated in the image below, which compares genuine and counterfeit blister packs (authentic on left, counterfeit on right).
Health Risks of Counterfeit Products
The counterfeit versions may contain undeclared tadalafil. Because tadalafil is a prescription-only medication, individuals who take nitrates or certain prescription drugs for heart disease, blood pressure, or other conditions may be at risk of life-threatening side effects such as dangerously low blood pressure or other serious adverse events.
What Consumers Should Do
Check your packaging: Confirm that your blister packs show one of the following Lot Numbers LOTGL0130151EXP0926; GL01EXP09/27; or GL110725 EXP110727
Immediately discontinue use of any product bearing the Lot number LOT308EXP03/28.
Report suspected counterfeit product directly to Green Lumber at [phone/email] and to the FDA’s MedWatch Adverse Event Reporting Program.
Seek medical care promptly if you experience unexpected side effects after using the mislabeled product.
Company Response
“Consumer safety is our number one priority,” said Brett Hales, President. “We acted swiftly after the FDA’s testing identified tadalafil in a product labeled as ours. Our investigation revealed that an employee had been diverting our packaging and customer channels to sell counterfeit goods. That individual has been terminated, and we have strengthened our safeguards to protect customers and ensure this does not happen again.”
Green Lumber has cooperated with the FDA and law enforcement from the beginning to address this matter and protect consumers.
Contact Information
Green Lumber Holding, LLC
Phone: 949.426.8622
Email: [email protected]
Website: www.greenlumber.com/alertExternal Link Disclaimer
FOR IMMEDIATE RELEASE – February 13, 2026 – North Kansas City, Missouri, Shaman Botanicals, LLC is voluntarily recalling one lot (Lot B# AAW
"Company Announcement
FOR IMMEDIATE RELEASE – February 13, 2026 – North Kansas City, Missouri, Shaman Botanicals, LLC is voluntarily recalling one lot (Lot B# AAW.501.3) of Alkaloids Chewable Tablets—White Vein to the consumer level. Recent testing showed that the Alkaloids Chewable Tablets—White Vein product contains 7-Hydroxymitragynine (7-OH) in an amount more than the declared value of 7.5 mg/tablet.
Risk Statement: Use of the Alkaloids Chewable Tablets—White Vein product could result in consumers ingesting a higher dose than intended, which could result in adverse health effects.
Shaman Botanicals, LLC has not received any reports of adverse events related to this lot of Alkaloids Chewable Tablets—White Vein.
The product is packaged in a 2-count bag with UPC Code 810057763724, in a 20-count bag with UPC Code 810057763830 and in a 30-count bottle with UPC Code 810057763779. The affected Alkaloids Chewable Tablets—White Vein lot has the following lot number: Lot B# AAW.501.3 (all expiration dates). The product can be identified by the lot number on the package and/or the bottom of the bottle. The Alkaloids Chewable Tablets—White Vein product was distributed nationwide to wholesalers, retailers, and consumers via online sales.
Shaman Botanicals, LLC is notifying its distributors and customers by email and is arranging for return of the affected product and providing refunds or replacement of all recalled products. Wholesalers, distributors, retailers, and consumers that have the Alkaloids Chewable Tablets—White Vein product that is being recalled should quarantine the product, stop using it, and return it to Shaman Botanicals, LLC.
To receive a full refund or replacement product, please go to the attached URL to register your return. https://recall.cbdamericanshaman.com/External Link Disclaimer.
Consumers with questions regarding this recall can contact Shaman Botanicals, LLC, Monday through Friday from 9am-5pm CST, at:
Vince Sanders c/o Quality Department
1501 Iron Street
North Kansas City, MO 64116
Telephone: 855-427-7386
Email: [email protected]
https://recall.cbdamericanshaman.com/External Link Disclaimer
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this dietary supplement product.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.
Complete and submit the report online: www.fda.gov/medwatch/report.htm
Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form or submit by fax to 1-800-FDA-0178.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration."
