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.

47,654 total recalls
2,552 in last 12 months

Showing 1504115060 of 27,451 recalls

Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (mono) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: NTEGRIS Allura 9 0 FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010/10 DRTable Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AlIura Xper F010 F Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci Si/X/Xi Surgical System Redundant Medical Grade Power Supply...

The Issue: Certain Redundant Medical Grade Power Supply (RMGPS) units specific to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Cesar Powerpack-Visub(V3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 Biplane DR Table Recalled by Philips Electronics North...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Cesar-DMCP-Visub(HM2000/3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AlluraXperFOlO/lO Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 F FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...

The Issue: Analyzers were distributed with software which lacks a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Haemonetics Corporation

Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...

The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...

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

Class II — Potential Health HazardOngoing