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. 2,653 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,653 in last 12 months

Showing 2304123060 of 51,768 recalls

FoodMay 22, 2019· ADM - CHICAGO

Recalled Item: Baker's Corner All Purpose Flour 5 lb. bag code: 041498130404 Recalled by...

The Issue: potential presence of E. coli. O26

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 22, 2019· ADM - CHICAGO

Recalled Item: Commander Flour Enr Recalled by ADM - CHICAGO Due to Potential E. coli...

The Issue: potential presence of E. coli. O26

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 22, 2019· ADM - CHICAGO

Recalled Item: Pillsbury BEST Bread Flour Enriched 5 LB bag code: 051500200315 Recalled by...

The Issue: potential presence of E. coli. O26

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 22, 2019· ADM - CHICAGO

Recalled Item: GWB Special Flour Bulk Product Code 803011 Recalled by ADM - CHICAGO Due to...

The Issue: potential presence of E. coli. O26

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 22, 2019· ADM - CHICAGO

Recalled Item: Latina Niagra Flour 50lbs bags Product Code 845202 Lot#: 8344BF Recalled by...

The Issue: potential presence of E. coli. O26

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 22, 2019· Abbott Laboratories

Recalled Item: "HEMOGLOBIN A1c CALIBRATORS *** *** 307261/R03 *** S4P5X0 Recalled by Abbott...

The Issue: Calibrator level 2 bottle may have been manufactured incorrectly for a...

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

Class II — Potential Health HazardOngoing
DrugMay 21, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: AMIKACIN SULFATE INJECTION Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 21, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: PROCHLORPERAZINE EDISYLATE INJECTION Recalled by Heritage Pharmaceuticals,...

The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2019· Dutch Ophthalmic USA, Inc.

Recalled Item: The device is a 25-gauge infusion line that is part Recalled by Dutch...

The Issue: Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Abbott Gmbh & Co. KG

Recalled Item: The Alinity ci-series System Control Modules which are configured with...

The Issue: All versions of the Alinity ci-series software may not detect an issue on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· DRG Instruments GmbH

Recalled Item: DRG Salivary Testosterone ELISA- IVD for the detection of Testerone Recalled...

The Issue: Salivary assay may observe a higher percentage of samples with 0 pg/ml...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· GE Healthcare, LLC

Recalled Item: LVivo EF app on Vscan Extend. Sold under the following Recalled by GE...

The Issue: Overestimation bias in automatically calculated ejection fraction (EF)...

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

Class II — Potential Health HazardOngoing
DrugMay 20, 2019· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 20, 2019· Medtronic Inc.

Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...

The Issue: Customers using the firm's continuous glucose monitoring system application...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Opternative Inc

Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...

The Issue: Lack of 510K clearance

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

Class II — Potential Health HazardOngoing