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. 2,567 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,567 in last 12 months

Showing 1442114440 of 27,451 recalls

Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Smooth Recalled by...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Pressure Sentinel¿ Intramedullary Reaming System Recalled by Zimmer...

The Issue: Various Trauma Guide Wires- creases in the sealing area on the end opposite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2018· Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...

The Issue: Software defect: For Helical scan with ClearView function, when small arc...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q.zen biplane with Material 10848355 - a Angiographic x-ray Recalled...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee biplane systems with Material 10094141- a Angiographic x-ray...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q biplane with Material 10848282- - a Angiographic x-ray Recalled by...

The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 10 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Slice (Air) Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 40 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· EUROTROL INC

Recalled Item: HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture....

The Issue: Incorrect measurement results caused by microbial contamination of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· EUROTROL INC

Recalled Item: HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture...

The Issue: Incorrect measurement results caused by microbial contamination of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Slice (Power) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: Falsely elevated (false positive) urobilinogen patient results due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-RFP-456 Recalled by NxStage Medical, Inc....

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing