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 2308123100 of 51,768 recalls

Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: GE Senographe Pristina - Product Usage: Senographe Pristina generates...

The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: GE Pristina Serena - Product Usage: Pristina Serena is an Recalled by GE...

The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Is a device that displays medical Recalled...

The Issue: There is the possibility of viewing studies directly from the Enterprise...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...

The Issue: There is the possibility of viewing studies directly from the Enterprise...

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

Class II — Potential Health HazardOngoing
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: Immulox Recalled by APS BioGroup, Inc Due to The recall is being conducted...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: DPS Throat Spray Recalled by APS BioGroup, Inc Due to The recall is being...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: Viralox Recalled by APS BioGroup, Inc Due to The recall is being conducted...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: Immuno PRP Spray Recalled by APS BioGroup, Inc Due to The recall is being...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· COOLHAUS

Recalled Item: Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Recalled by...

The Issue: Product contains undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 15, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C...

The Issue: Observed reported incidence rate for harm associated with intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C...

The Issue: Observed reported incidence rate for harm associated with intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C...

The Issue: Observed reported incidence rate for harm associated with intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2019· Medtronic Neuromodulation

Recalled Item: InterStim(TM) System Recalled by Medtronic Neuromodulation Due to There is a...

The Issue: There is a potential for an unexpected increase in stimulation during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2019· Edwards Lifesciences, LLC

Recalled Item: IntraClude Intra-Aortic Occlusion Device Recalled by Edwards Lifesciences,...

The Issue: Possibility of balloon rupture in intra-aortic occlusion devices. If the...

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

Class I — Serious Health HazardOngoing
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· American Health Packaging

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by American Health Packaging...

The Issue: GMP Deviations; possible cross contamination of product due to cleaning...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· MALLINCKRODT PHARMACEUTICALS

Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...

The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2019· MALLINCKRODT PHARMACEUTICALS

Recalled Item: Amitiza (lubiprostone) capsules Recalled by MALLINCKRODT PHARMACEUTICALS Due...

The Issue: Labeling: Label mix-up. Amitiza 8 mcg capsules are being recalled because 24...

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

Class II — Potential Health HazardOngoing
Refund