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. 1,965 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,965 in last 12 months

Showing 1956119580 of 29,208 recalls

Medical DeviceDecember 1, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 722012 is intended for: Cardiovascular and vascular...

The Issue: Due to a production error, screws were not tightened to specified torque....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and Recalled by...

The Issue: Due to a production error, screws were not tightened to specified torque....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Merit Medical Systems, Inc.

Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...

The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Pride Mobility Products Corp

Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...

The Issue: The interface between the TB3 back and tilt base can separate when tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD10 722026 is intended for: Cardiovascular and vascular...

The Issue: Due to a production error, screws were not tightened to specified torque....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Pediatric Chamber Ocean Drains as follows: 2012-320 Ocean...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes VA Implant Rack for the Compact Distal Radius System Recalled by...

The Issue: The screw rack plate was assembled incorrectly which could cause the screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Single Drain as follows: 3600-100 Oasis single Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: CentraLink¿ Data Management System Software Versions: v13x Recalled by...

The Issue: There is a remote possibility CentraLink may download an order to the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Oasis Blood Recovery Drains as follows: 3650-100 Oasis...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical Dual Chamber Ocean Drains as follows: 2020-000 Ocean Recalled...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2016· Atrium Medical Corporation

Recalled Item: Atrium Medical 400 Series Express Drains as follows: 4000-100N Express...

The Issue: Outer Packaging is not sterile

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

Class II — Potential Health HazardOngoing