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. 2,724 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,724 in last 12 months

Showing 1838118400 of 51,768 recalls

Medical DeviceAugust 14, 2020· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...

The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Battelle Memorial Institute

Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...

The Issue: Masks processed at one site were not maintained at levels of condensation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Sobel Westex

Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...

The Issue: Due to non-surgical isolation gowns not meeting all performance test...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Pharmaceutical Innovations, Inc.

Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...

The Issue: The firm registered the product as a Class I device, but has since been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker IsoAir 2.0 support surface-provides pressure redistribution and is...

The Issue: Connector between support surface and pump may be out of tolerance resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrognease P-L Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2020· Randox Laboratories Ltd.

Recalled Item: Lactate Dehydrogenase L-P Recalled by Randox Laboratories Ltd. Due to An...

The Issue: An update to the carryover avoidance technical bulletin to introduce...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Aurobindo Pharma USA...

The Issue: Presence of Foreign Substance: product complaints were received by the firm...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2020· Sanofi-Aventis U.S. LLC

Recalled Item: Elitek (rasburicase) for injection Recalled by Sanofi-Aventis U.S. LLC Due...

The Issue: Failed Stability Specifications: Out of Specification result for enzyme...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2020· Lannett Company, Inc.

Recalled Item: Prednisone Tablets Recalled by Lannett Company, Inc. Due to Labeling: Label...

The Issue: Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 10, 2020· Whole Foods Market

Recalled Item: Whole Foods Market Mitica La Dama Sagrada Raw Milk - Recalled by Whole Foods...

The Issue: Undeclared lysozyme (from egg whites)

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

Class I — Serious Health HazardOngoing
Refund