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. 2,794 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,794 in last 12 months

Showing 97019720 of 29,208 recalls

Medical DeviceMay 14, 2021· Smiths Medical ASD Inc.

Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...

The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2021· Brainlab AG

Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...

The Issue: Display of potential patient movement might be delayed to the user for high...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· W L Gore & Associates, Inc.

Recalled Item: Gore Propaten Vascular Graft configured for Pediatric Shunt Recalled by W L...

The Issue: Vascular Grafts containing an inner diameter of 6 mm may be incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· W L Gore & Associates, Inc.

Recalled Item: Gore Propaten Vascular Graft configured for Pediatric Shunt Recalled by W L...

The Issue: Vascular Grafts containing an inner diameter of 6 mm may be incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Michael Graves with Stryker Highback Chair-intended for pediatric and adult...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: InTouch 2131-intended to support a human patient in an acute care setting...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing