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. 1,157 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,157 in last 12 months

Showing 2901–2920 of 51,768 recalls

DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Haloperidol Decanoate Injection Recalled by Somerset Therapeutics Private...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 650 SE Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750c A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
DrugMarch 21, 2025· Somerset Therapeutics Private Limited

Recalled Item: Methocarbamol Injection USP 1 Recalled by Somerset Therapeutics Private...

The Issue: Lack of Assurance of Sterility: Media fill with bacterial contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 650c A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 620 A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
DrugMarch 21, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Venlafaxine Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Presence of Foreign Substance: Product complaint received for the presence...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750 A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· Radiometer Medical ApS

Recalled Item: Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090...

The Issue: ABL90 FLEX and ABL90 FLEX PLUS analyzers running with Radiometer Windows 10...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2025· Abbott Molecular, Inc.

Recalled Item: The Alinity m System is designed to automate the steps Recalled by Abbott...

The Issue: The design of the Alinity m System Solutions drawer enclosure may allow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2025· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...

The Issue: There have been at least 12 complaints from users as of March 3, 2025,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2025· Channel Medsystems, Inc.

Recalled Item: Brand Name: Cerene Cryotherapy Device Product Name: DEVICE Recalled by...

The Issue: Due to evaporator gasket not sealing which can cause liquid nitrous oxide to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM Crea Test Card (25 pk) for the epoc Blood Analysis System Recalled...

The Issue: The occurrence of discrepant high pH results in samples introduced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing