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 1741–1760 of 17,529 recalls
Recalled Item: Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose
The Issue: Lack of Assurance of Sterility: Potential presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution 1.5% Dextrose
The Issue: Lack of Assurance of Sterility: Potential presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075%
The Issue: Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0%
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: hello wild strawberry fluoride toothpaste
The Issue: Labeling: Label Mix-Up: Some hello wild strawberry fluoride
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: activator concentrate
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lugol's (Strong Iodine Solution USP)
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AstrinGyn (Ferric Subsulfate) Aqueous
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALCOLADO RELAMPAGO (Menthol and Camphor)
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blis-To-Sol Liquid (Tolnaftate)
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unguentine Ointment
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively
The Issue: CGMP Deviations: Products not manufactured under current good
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PLUVICTO 1
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: Vegetal Vigra
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rasagiline Tablets 0.5mg
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Pain Relieving Cream (Menthol 7.4%)
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Tri-Active Therapy Cream (Camphor 3.2%
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix CBD Therapy Cream (Menthol 7.4%)
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix CBD Clinical Cream (Menthol 7.4%)
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%)
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP
The Issue: Labeling: Not Elsewhere Classified - the description, warnings,
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.