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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18881–18900 of 47,654 recalls
Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Extra Strength Acetaminophen Tablets Recalled by Contract Pharmacal...
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Extra Strength Acetaminophen Tablets Recalled by Contract Pharmacal...
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by Pfizer Inc. Due to Defective Container:...
The Issue: Defective Container: confirmed customer reports for vials with loose metal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ABL90 FLEX PLUS Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal PS Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: New! Rompe Pecho MAX Multi Symptoms Recalled by Efficient Laboratories, Inc....
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rompe Pecho EX Expectorant Recalled by Efficient Laboratories, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rompe Pecho CF Cold & Flu with Honey Recalled by Efficient Laboratories,...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethacrynate Sodium for Injection Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile Recalled by Applied...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Procedure Packs containing AAMI Level 3 surgical gowns Recalled by...
The Issue: The kits contained recalled surgical gowns. The gowns were manufactured at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Procedure Packs containing AAMI Level 3 surgical gowns Recalled by...
The Issue: The kits contained recalled surgical gowns. The gowns were manufactured at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink 2090 Programmer. Used to interrogate and program...
The Issue: Medtronic Conexus Telemetry has been determined to contain two primary cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink Encore 29901 Programmer. Used to interrogate and program...
The Issue: Medtronic Conexus Telemetry has been determined to contain two primary cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.