Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22661–22680 of 47,654 recalls
Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules USP Recalled by Dr. Reddy's...
The Issue: Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 Units added to NS 500 mL (oxytocin and Recalled by Advanced...
The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gel Hand Sanitizer (Ethyl Alcohol 70%) Recalled by Ecolab Inc Due to...
The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advanced Gel Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc Due...
The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...
The Issue: Potential compromise of product sterility after routine monitoring for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...
The Issue: Potential esophageal laceration during a patient procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moisturizing Lubricant Eye Drops Recalled by Akorn Inc Due to Failed...
The Issue: Failed Stability Specification: out of specification results for Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levoleucovorin Injection Recalled by Mylan Institutional Inc Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as copper salts
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray...
The Issue: Defective Container: Potential for broken glass in the neck area of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...
The Issue: The products were manufactured without a back bevel on the needle tip. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...
The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...
The Issue: Potential for the Semi-Rigid canister lid to fragment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Dr. Reddy's...
The Issue: Failed Dissolution Specifications: Out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.