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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16721–16740 of 47,654 recalls
Recalled Item: Best Choice Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kaiser Permanente Clotrimazole Cream USP Recalled by Taro Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equate Athlete's Foot Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: H-E-B - Athlete's Foot Cream Clotrimazole Cream USP Recalled by Taro...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Recalled by Fresenius...
The Issue: Cross Contamination with other products: trace amounts of lidocaine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARIPIPRAZOLE TABLETS Recalled by Golden State Medical Supply Inc. Due to...
The Issue: FAILED DISSOLUTION SPECIFICATIONS: Possibility of out-of-specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel Recalled by MPM...
The Issue: Microbial Contamination of Non-Sterile Drug Product. The product was found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...
The Issue: Cross Contamination with Other Products: trace amounts of octreotide found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE...
The Issue: The firm is recalling their products due the unapproved use of a food...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...
The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.