Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,958 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,958 in last 12 months

Showing 2034120360 of 29,208 recalls

Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Cepheid

Recalled Item: Xpert MRSA Catalog GXMRSA-120 Recalled by Cepheid Due to Internal...

The Issue: Internal investigation found the certain lots of MRSA kits have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330NR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Spine. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: Synergy Cranial S7. The software application is sent in CD format with an...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Medtronic Navigation, Inc.

Recalled Item: S7 MACH FrameLink. The software application is sent in CD format with an IFU...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...

The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-330BR Bovie Precise 360 Handpiece 33cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas p 471 centrifuge unit calculator/data processing module Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 8000 Modular Analyzer Series c8000 Recalled by Roche Diagnostics...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: RSD 800 Sorting System calculator/data processing module Recalled by Roche...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6000 Series system c6000 Recalled by Roche Diagnostics Operations,...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A Recalled by...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Topcon Medical Laser Systems, Inc

Recalled Item: Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The...

The Issue: Topcon discovered an anomaly with titration, only when EpM is turned on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Hill-Rom, Inc.

Recalled Item: Affinity Four Birthing Bed Model P3700 The primary packaging is Recalled by...

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

Class II — Potential Health HazardOngoing