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. 2,635 recalls have been distributed to District of Columbia in the last 12 months.
Showing 4621–4640 of 47,654 recalls
Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump 371 14F LT CMR Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 Set AU Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empower Pharmacy Recalled by EMPOWER CLINIC SERVICES LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...
The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection) Recalled by...
The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Tablets Recalled by Amneal Pharmaceuticals, LLC Due to Presence...
The Issue: Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV LL 18X103- Wallflex Esophageal Partially Recalled...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGILE ESO OTW PC 23MM X 6.2CM IN 18.5 FR- Recalled by Boston Scientific...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX PC ESOPH STENT 23/28MM X 105MM- Wallflex Esophageal Partially...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX ESOPHAGEAL FC 23/28MMX12CM- Wallflex Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX ESOPHAGEAL FC 18/23-25MMX15CM- Agile Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV LL 23X155- Wallflex Esophageal Partially Recalled...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 instrument -Intended for the rapid identification (ID)...
The Issue: Escherichia coli (E. coli) misidentification for clinical samples that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX ESOPHAGEAL FC 23/28MMX15CM-Wallflex Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX PC ESOPH STENT 18/23MM X 123MM- Wallflex Esophageal Partially...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV 18X103MM- Wallflex Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.