Drug Recalls
Here you'll find every drug recall the FDA has issued, including prescription medications, over-the-counter drugs, compounded pharmacy products, and dietary supplements. We've been tracking these since 2006 and our database updates several times a day so you're always looking at current information.
Drugs get recalled for a number of reasons: contamination during manufacturing, incorrect potency or dosage, failed quality testing (like dissolution or stability tests), sterility problems in injectable products, or labeling and packaging errors that could cause someone to take the wrong dose. If you find a product on this list that you use, please follow the instructions provided by the FDA to take the necessary precautions.
Showing 16821–16840 of 17,529 recalls
Recalled Item: Aniracetam and Choline
The Issue: Marketed Without an Approved NDA/ANDA: The products are
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOOTROPA COGNITIVE ENHANCEMENT SUPPLEMENT
The Issue: Marketed Without an Approved NDA/ANDA: The products are
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piracetam & Choline
The Issue: Marketed Without an Approved NDA/ANDA: The products are
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS
The Issue: Presence of Foreign Substance: Reports of gray smudges
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BoostYourGrade.com
The Issue: Marketed Without an Approved NDA/ANDA: The products are
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetic Acid Otic Solution
The Issue: Subpotent Drug: The product/lot is out-of-specification (OOS) for
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Night Bullet Capsules
The Issue: Marketed Without an Approved NDA/ANDA; product contains analogues
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin
The Issue: Lack of Assurance of Sterility; product linked to
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifadin
The Issue: Subpotent drug: low fill volume in some of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nupercainal
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myoflex (trolamine salicylate) 10%
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Fast Acting Nasal Spray
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Menthol Nasal Spray
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Saline Moisturizing Mist with Eucalyptol & Menthol
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol)
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)
The Issue: Labeling: Not Elsewhere Classified: This product is misbranded
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.