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. 2,612 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,612 in last 12 months

Showing 3124131260 of 51,768 recalls

Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: XARIO 100 TUS-X100 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Skewers Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO 300 TUS-A300 diagnostic ultrasound system Recalled by Toshiba American...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: LapSac Introducer Set Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Circadiance LLC

Recalled Item: SmartMonitor 2 PS/PSL Recalled by Circadiance LLC Due to Circadiance has...

The Issue: Circadiance has determined that it is possible for certain Smart Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Plate Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Set Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 Recalled by Toshiba...

The Issue: When Continuous Trace method is used as the tracing method on Spectral...

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

Class II — Potential Health HazardOngoing
FoodMay 1, 2017· Herbalife International Of America Inc

Recalled Item: Protein Bar 14 bars/box Recalled by Herbalife International Of America Inc...

The Issue: Herbalife is recalling Protein Bar-Peanut Butter because it may contain a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugMay 1, 2017· Allergan Sales, LLC

Recalled Item: Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic...

The Issue: Failed Impurities/Degradation Specifications: stability testing results did...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2017· PAR Sterile Products LLC

Recalled Item: Buprenorphine HCI Injection Recalled by PAR Sterile Products LLC Due to...

The Issue: Crystallization: due to the presence of white, crystalline particulates,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: TIBIAL I/M NAIL 15MMDX26CM Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: FEM IM NAIL 14MMDX30CM LEFT Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSA-FX II STD TUBE 130DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...

The Issue: Mindray has received two reports from outside the United States that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: FEM IM NAIL 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: R-F IM NAIL 10MMDX48CM LG Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· Zimmer Biomet, Inc.

Recalled Item: 4.5 BROAD SCP PLT 26-H STER Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...

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

Class II — Potential Health HazardOngoing