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. 2,469 recalls have been distributed to Washington in the last 12 months.
Showing 861–880 of 51,768 recalls
Recalled Item: MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software...
The Issue: A software timing and processor communication issue in MiniMed" 780G...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nivagen Pharmaceuticals Recalled by Blossom Pharmaceuticals Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dynashield Skin Protectant Recalled by Blossom Pharmaceuticals Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wecare Enema Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WeCare Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dynashield Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Globe Zinc Oxide Ointment USP Zinc Oxide 20% Skin Protectant Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lumify Diagnostic Ultrasound System models : 795005 Recalled by Philips...
The Issue: Ultrasound system compatibility issues with Apple devices running iOS 18 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX800. Product Number: 865240. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phytonadione Injectable Emulsion Recalled by Cipla Limited Due to Failed...
The Issue: Failed Stability Specifications: Observed OOS results: eg results for colour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Arise 1000EX mattress Recalled by Stryker Medical Division of...
The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MV3 bariatric bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX100. Product Number: 867033. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OER-Elite Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP60. Product Number: M8005A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nivagen Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP90. Product Number: M8010A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP30. Product Number: M8002A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.