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. 1,923 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,923 in last 12 months

Showing 2630126320 of 29,208 recalls

Medical DeviceAugust 26, 2013· Bayer Healthcare Llc

Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...

The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Zimmer, Inc.

Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...

The Issue: Possibility of the weld to the quick-connect breaking when force is applied...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2013· Medtronic Xomed, Inc.

Recalled Item: Universal Titanium Prosthesis Recalled by Medtronic Xomed, Inc. Due to One...

The Issue: One lot of the product was assembled using the Cam Head version of the same...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· Ebi, Llc

Recalled Item: BIOMET Spine Recalled by Ebi, Llc Due to Polaris Translation Screw Failures...

The Issue: Polaris Translation Screw Failures were recently reported to Biomet Spine....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· Trans American Medical, Inc.

Recalled Item: Spectre Wireless Footswitch/Handswitch system Model 98/99 Recalled by Trans...

The Issue: TransAmerican Medical Imaging is recalling certain lots of TMI Spectre...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· ITC-Nexus Dx

Recalled Item: Surgicutt fully automated incision making device for bleeding time...

The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.33 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Combo 3 Sold outside of US only. Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 1 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Combo 2 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Urine Combo 4 Sold outside of US Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Breakpoint Combo 4 Sold outside of US Recalled by...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Breakpoint Combo 7 Product Usage:...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2013· Bio-Rad Laboratories

Recalled Item: FSE Image Upgrade Kit Recalled by Bio-Rad Laboratories Due to The FSE Image...

The Issue: The FSE Image Upgrade kit (part 92019C) is recalled due to issue related to...

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

Class III — Low RiskOngoing
Medical DeviceAugust 20, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX Evolution System (Standard Q) The DRX-Evolution System...

The Issue: Carestream received a report of an exposure being initiated without a...

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

Class II — Potential Health HazardOngoing