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 10041–10060 of 17,529 recalls
Recalled Item: 0.9% Sodium Chloride Injection USP
The Issue: Lack of Assurance of Sterility: Customer complaints for
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection
The Issue: Lack of Assurance of Sterility: Bags have the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection
The Issue: Lack of Assurance of Sterility: Bags have the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: D-ZINE Rapid Size and Strength capsules
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA-STEN Rapid Size and Strength capsules
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Oral Suspension
The Issue: Labeling Error: Label mix-up. Products' unit dose cups
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per Bottle
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Obagi-C Rx System C-Therapy Night Cream
The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...
The Issue: Presence of Foreign Substance: possibility of the presence
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution
The Issue: Microbial contamination of non-sterile product: product failed Total
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution
The Issue: Microbial contamination of non-sterile product: product failed Total
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine Chloride Injection (Preserved) 20 mg per mL
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection
The Issue: Lack of Assurance of Sterility; media fill failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.