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. 1,939 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,939 in last 12 months

Showing 2236122380 of 29,208 recalls

Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...

The Issue: When performing head or neck scans, the currently displayed SAR values could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Elekta, Inc.

Recalled Item: XiO Radiation Treatment Planning System. Used to create treatment plans...

The Issue: Incorrect Treatment Delivery Using Third Party Fixed Wedges.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: Recalled...

The Issue: The Synthes Cranial Flap Tube Clamp and Crimping Device for Cranial Tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Beckman Coulter Inc.

Recalled Item: Access Free T3 Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter, Inc. is recalling Access Free T3 Reagent Kit because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConForMIS Unicondylar Knee Replacement System iUNI G2 Recalled by ConforMIS,...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· ConforMIS, Inc.

Recalled Item: ConFormis iDUO G2 Recalled by ConforMIS, Inc. Due to May contain small...

The Issue: May contain small amounts of ethylene glycol residue

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Medical Systems Duodenoscope Recalled by Fujifilm Medical Systems...

The Issue: A precautionary measure because the Duodenoscopes have been redesigned to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2015· Becton Dickinson & Co.

Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...

The Issue: BD has confirmed that a portion of tests associated with the affected lots(...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...

The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.

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

Class III — Low RiskOngoing
Medical DeviceAugust 27, 2015· Arrow International Inc

Recalled Item: Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes...

The Issue: Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to...

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

Class II — Potential Health HazardOngoing