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 1526115280 of 51,768 recalls

Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence with software syngo.CT VB20 Model #10590100 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive with software syngo.CT VB20 Model #10431700 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 Recalled by...

The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK LOGIC Polyethylene Tibial Inserts Recalled by Exactech, Inc. Due to...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX Recalled by...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: TRULIANT Knee System including TRULIANT Tibial Inserts Recalled by Exactech,...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System custom devices labeled as the following:...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System Recalled by Exactech, Inc. Due to Inserts...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2021· Exactech, Inc.

Recalled Item: OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial...

The Issue: Inserts were packaged in vacuum bags that lacked an additional oxygen...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Chlorzoxazone Tablets USP 750 mg 100 Tablets Rx Only NDC Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Fulvestrant Injection 250 mg/5 mL (50 mg/mL) For Intramuscular Use Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules USP 50 mg 100 Capsules Rx Only NDC Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules USP 100 mg Rx Only Manufactured by: Glenmark Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2021· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund