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. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1600116020 of 51,768 recalls

Medical DeviceJune 7, 2021· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel plus (Pneumoplus) Part Numbers: Part No:...

The Issue: Due to real-time stability study failures resulting in increase rate of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2021· Pear Therapeutics, Inc.

Recalled Item: reSET-O Mobile App Recalled by Pear Therapeutics, Inc. Due to Due to a...

The Issue: Due to a software issue, patients with a urine drug screen (UDS) received...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2021· Pear Therapeutics, Inc.

Recalled Item: reSET Mobile App Recalled by Pear Therapeutics, Inc. Due to Due to a...

The Issue: Due to a software issue, patients with a urine drug screen (UDS) received...

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

Class II — Potential Health HazardOngoing
DrugJune 4, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: due to presence of ATV cyclo...

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

Class III — Low RiskOngoing
Refund
FoodJune 4, 2021· Bomunity Ltd Co

Recalled Item: Paximune Dietary Supplement Contains Bovine Proteins that help Promote...

The Issue: Potential to be contaminated with bacteria

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2021· Simpleware Product Group, SYNOPSYS NORTHERN EUROPE

Recalled Item: Simpleware ScanIP software. For transfer of imaging information from a...

The Issue: A issue (bug) has been identified with the interface and image software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Simpleware Product Group, SYNOPSYS NORTHERN EUROPE

Recalled Item: Simpleware ScanIP medical software. For transfer of imaging information from...

The Issue: A issue (bug) has been identified with the interface and image software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Eight Medical International BV

Recalled Item: Recirculator 8.0s Disposable Lavage Kit (product code number 8100) Recalled...

The Issue: The patient may be exposed to potential aluminum ion release during warming...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus Stapler-intended for transection Recalled by...

The Issue: Mislabeled: Labeled on the package as 60mm contains 45mm devices

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Outflow Graft Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Accessories Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Implant Kit Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Implant Kit Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Axonics Modulation Technologies, Inc.

Recalled Item: BULKAMID Recalled by Axonics Modulation Technologies, Inc. Due to Lack of...

The Issue: Lack of Sterility Assurance; needle in procedure pack labeled as sterile may...

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

Class II — Potential Health HazardOngoing