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Drug Recall Records

This page shows recent human drug recall alerts sourced from the FDA. It includes current and some previously imported records, but is not a complete historical archive of all past recalls. For full historical data, visit the official FDA Drug Recalls page. Always consult a healthcare professional for medical advice.

By Dosage Form:
AllTabletsCapsulesInjectables
By Recall Category:
AllContamination / SterilityLabeling / PackagingUndeclared Ingredient
Kian Pee Wan – Dietary supplement capsules marketed for treatment for gaining weight and stimulating appetite.
Date: 04/01/2026
Brand: Kian Pee Wan
Product: Dietary supplement capsules marketed for treatment for gaining weight and stimulating appetite.
Company: Aphreseller
Recall Reason: Device & Drug Safety/Unapproved Drug
Dosage Form: Capsule
Category: Other Recall Issue
View Details View FDA Recall Listings
Amneal – Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag
Date: 03/24/2026
Brand: Amneal
Product: Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag
Company: Amneal Pharmaceuticals LLC
Recall Reason: A Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid in 0.7% Sodium Chloride Injection, 10 mg/mL.
Dosage Form: Injection
Category: Other Recall Issue
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Webcol – Large Alcohol Prep Pads (70% isopropyl alcohol)
Date: 03/20/2026
Brand: Webcol
Product: Large Alcohol Prep Pads (70% isopropyl alcohol)
Company: Cardinal Health
Recall Reason: Microbial Contamination
Dosage Form: Other / Unspecified
Category: Contamination / Sterility
View Details View FDA Recall Listings
Green Lumber – Dietary Supplement
Date: 02/13/2026
Brand: Green Lumber
Product: Dietary Supplement
Company: Green Lumber Holding, LLC.
Recall Reason: Undeclared prescription drug-Tadalafil
Dosage Form: Other / Unspecified
Category: Undeclared / Unapproved Ingredient
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Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle, Rx
Date: 01/21/2026
Product: Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIS LTD., Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India, Manufactured for: UNICHEM PHARMACEUTICALS (USA), INC., East Brunswick, NJ 08816, NDC 29300-187-01
Company: Unichem Pharmaceuticals USA Inc.
Recall Reason: cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
Category: Class II
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Modern Warrior – Dietary supplement capsules marketed for metabolism moosting, improving brain function, and reducing cravings
Date: 01/09/2026
Brand: Modern Warrior
Product: Dietary supplement capsules marketed for metabolism moosting, improving brain function, and reducing cravings
Company: Modern Warrior
Recall Reason: Unapproved new drug found to contain undeclared 1,4-DMAA and aniracetam, and tianeptine
Dosage Form: Capsule
Category: Undeclared / Unapproved Ingredient
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Silintan – Dietary supplement capsules marketed for relief of joint and body aches
Date: 01/09/2026
Brand: Silintan
Product: Dietary supplement capsules marketed for relief of joint and body aches
Company: Anthony Trinh, 123Herbals LLC
Recall Reason: Unapproved new drug found to contain undeclared meloxicam
Dosage Form: Capsule
Category: Undeclared / Unapproved Ingredient
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Virgo – Rheumacare Capsules
Date: 12/22/2025
Brand: Virgo
Product: Rheumacare Capsules
Company: Handelnine Global Limited d/b/a Navafresh
Recall Reason: Elevated levels of lead
Dosage Form: Capsule
Category: Other Recall Issue
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MR7 Super 700000 – Dietary supplement for male enhancement
Date: 12/16/2025
Brand: MR7 Super 700000
Product: Dietary supplement for male enhancement
Company: StuffbyNainax LLC
Recall Reason: Undeclared Sildenafil and Tadalafil
Dosage Form: Other / Unspecified
Category: Undeclared / Unapproved Ingredient
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ICU Medical – 20 mEq Potassium Chloride Injection
Date: 11/03/2025
Brand: ICU Medical
Product: 20 mEq Potassium Chloride Injection
Company: Otsuka ICU Medical LLC
Recall Reason: Potential for Potassium chloride overdose: 20 mEq Potassium Chloride Injection is Mislabeled As 10 mEq Potassium Chloride Injection
Dosage Form: Injection
Category: Labeling / Packaging
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Semaglutide Injection, 10 mg/4 mL (2.5 mg/mL), 4mL Multidose Vial, For Subcutaneous
Date: 10/15/2025
Product: Semaglutide Injection, 10 mg/4 mL (2.5 mg/mL), 4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341.  NDC:  84139-225-04
Company: ProRx LLC
Recall Reason: Lack of Assurance of Sterility
Category: Class II
View Details View FDA Recall Listings
Reconstitution XO Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840
Date: 07/30/2025
Product: Reconstitution XO Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health a) 5% Exosomes, 10 mL vial and b) 10% Exosomes, 5 mL vial, Extension Health a) 20% Exosomes, 10 mL vial, b) 10% Exosomes, 10 mL vial and Medical Health Institute (MHI), a) 10 % Exosomes, 2mL vial, 5mL vial, 10mL vial, b) 5% Exosomes, 2mL vial, 5mL vial, 10mL vial.
Company: GenoGenix  LLC
Recall Reason: Lack of Assurance of Sterility
Category: Class II
View Details View FDA Recall Listings
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