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 6161–6180 of 17,529 recalls
Recalled Item: Sildenafil 200 mg Troche (Clinic)
The Issue: Labeling: Incorrect or missing lot and/or expiration date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone 50 mg capsules
The Issue: Labeling: Incorrect or missing lot and/or expiration date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine (T3) 92.5 MCG
The Issue: Labeling: Incorrect or missing lot and/or expiration date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DHEA/Pregnenol One 10.25 MG Cap
The Issue: Labeling: Incorrect or missing lot and/or expiration date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tadalafil 20 mg Troche
The Issue: Labeling: Incorrect or missing lot and/or expiration date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T3/T4 SR 9 mcg/38 mcg capsule
The Issue: Labeling: Incorrect or missing lot and/or expiration date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 30000 Capsules
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: Glenmark Ranitidine Tablets USP 150 mg Rx Only 500 Tablets
The Issue: CGMP Deviations: Presence of NDMA impurity detected in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull Platinum 30000 Capsules
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: Ketorolac Tromethamine Injection
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stallion Platinum 30000 Capsules in blue
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: Panther Platinum 30000 Capsules
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: Ketorolac Tromethamine Injection
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Ranitidine Tablets USP 300 mg Rx Only 250 Tablets
The Issue: CGMP Deviations: Presence of NDMA impurity detected in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Ranitidine Tablets USP 300 mg Rx Only 100 Tablets
The Issue: CGMP Deviations: Presence of NDMA impurity detected in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Ranitidine Tablets USP 150 mg Rx Only 60 Tablets
The Issue: CGMP Deviations: Presence of NDMA impurity detected in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Ranitidine Tablets USP 150 mg Rx Only 100 Tablets
The Issue: CGMP Deviations: Presence of NDMA impurity detected in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Ranitidine Tablets USP 300 mg Rx Only 30 Tablets
The Issue: CGMP Deviations: Presence of NDMA impurity detected in
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocortisone and Acetic Acid Otic Solution
The Issue: Subpotent Drug: Low Out of specification (OOS) assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.