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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,485 in last 12 months

Showing 1982119840 of 27,451 recalls

Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego (system Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Possible leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Villa Radiology Systems LLC

Recalled Item: Apollo EZ: Model: 9784152036 Multi-function x-ray systems capable of routine...

The Issue: The analysis showed that the incident was caused by a chain of four faults:...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Horiba Instruments Inc

Recalled Item: Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 Recalled by Horiba...

The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis (system Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Possible leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Villa Radiology Systems LLC

Recalled Item: Apollo: Models: 9784000131 Recalled by Villa Radiology Systems LLC Due to...

The Issue: The analysis showed that the incident was caused by a chain of four faults:...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Villa Radiology Systems LLC

Recalled Item: Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of...

The Issue: The analysis showed that the incident was caused by a chain of four faults:...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Villa Radiology Systems LLC

Recalled Item: Juno DRF Recalled by Villa Radiology Systems LLC Due to The analysis showed...

The Issue: The analysis showed that the incident was caused by a chain of four faults:...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Integrated Science Systems Inc

Recalled Item: Sure Vue Color Staph 150T Recalled by Integrated Science Systems Inc Due to...

The Issue: Customer complaints of very weak reactions with the kit, or false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Mckesson Medical Immaging

Recalled Item: McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including...

The Issue: McKesson has identified a design deficiency where under rare circumstances,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: 1) VITROS¿ Immunodiagnostic Products Total Beta-hCG II Reagent Pack (Unique...

The Issue: When testing was conducted using certain lots, VITROS¿ Systems generated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing