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. 2,728 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,728 in last 12 months

Showing 1786117880 of 51,768 recalls

DrugOctober 27, 2020· Sunstar Americas, Inc.

Recalled Item: Paroex (chlorhexidine gluconate) Oral Rinse Recalled by Sunstar Americas,...

The Issue: Microbial Contamination of Non-sterile Products: contamination with...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 27, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg Recalled by...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2020· Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers

Recalled Item: Natural Grocers Recalled by Vitamin Cottage Natural Foods Market, Inc DBA...

The Issue: Potential contamination with Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2020· Philips Ultrasound Inc

Recalled Item: All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G Recalled...

The Issue: The manufacturer has determined that with certain uncommon workflows there...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2020· GE Healthcare, LLC

Recalled Item: MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient...

The Issue: Incorrect patient identification and/or patient demographic errors.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2020· Mani, Inc. - Kiyohara Facility

Recalled Item: MANI Infusion Cannula 23G S - Product Usage: for use Recalled by Mani, Inc....

The Issue: Dimensions of the Luer connector parts out of specification, may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2020· Mani, Inc. - Kiyohara Facility

Recalled Item: MANI TROCAR KIT 23G S - Product Usage: for use Recalled by Mani, Inc. -...

The Issue: Dimensions of the Luer connector parts out of specification, may cause...

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

Class II — Potential Health HazardOngoing
DrugOctober 26, 2020· Ascent Pharmaceuticals, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...

The Issue: Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2020· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Olanzapine Orally Disintegrating Tablets Recalled by Jubilant Cadista...

The Issue: Subpotent

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 26, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...

The Issue: Test Definition scanning may reset custom settings to defaults causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer - Product Usage: automated Recalled by Siemens...

The Issue: Test Definition scanning may reset custom settings to defaults. When a 2D...

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2020· Heritage Pharmaceuticals Inc

Recalled Item: Felodipine Extended Release Tablets Recalled by Heritage Pharmaceuticals Inc...

The Issue: Failed impurities/ degradation specifications: Out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2020· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2020· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 23, 2020· Hardy Diagnostics

Recalled Item: Viral Transport Medium Recalled by Hardy Diagnostics Due to There is a...

The Issue: There is a potential for contamination within Viral Transport Media. Use of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Medtronic Heart Valves Division

Recalled Item: Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23...

The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Medtronic Heart Valves Division

Recalled Item: Evolut (TM) PRO+ System. With the following model numbers: a. Recalled by...

The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Medtronic Heart Valves Division

Recalled Item: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...

The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Biomeme, Inc.

Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...

The Issue: The firm has become aware of nine reports by a single customer that the...

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

Class II — Potential Health HazardOngoing