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. 2,565 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,565 in last 12 months

Showing 1458114600 of 27,451 recalls

Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 40mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 14mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 12mm x 30mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 12mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Giraffe Warmer. Device sold under the following product names: Giraffe...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 4mm x 20mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver Biliary 518 Stent 5mm x 60mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 20mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 518 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Cook Medical Incorporated

Recalled Item: Zilver 635 Biliary Stent 5mm x 80mm Recalled by Cook Medical Incorporated...

The Issue: The instruction for use detail, with respect to removal of the delivery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda Wall Mount warmer. Infant radiant warmer Recalled by GE Healthcare,...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· GE Healthcare, LLC

Recalled Item: Panda iRes Infant Radiant Warmer. Device sold under the following Recalled...

The Issue: Potential electric leakage affecting the user.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2018· Pro-Dex Inc

Recalled Item: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack...

The Issue: Visual particulates within a battery Tyvek pouch. The battery is provided...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001...

The Issue: Limits of Detection (LoD) for protein, nitrite, leukocytes, and erythrocytes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Reader Spare Part Recalled by Becton Dickinson & Co. Due...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2018· Becton Dickinson & Co.

Recalled Item: BD Max Instrument Recalled by Becton Dickinson & Co. Due to A trend for...

The Issue: A trend for false positive Candida glabrata results has been confirmed. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing