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. 1,112 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,112 in last 12 months

Showing 15501–15520 of 51,768 recalls

Medical DeviceAugust 6, 2021· Philips Ultrasound Inc

Recalled Item: Affiniti Diagnostic Ultrasound Systems: Software Versions 5.0 Recalled by...

The Issue: Due to a software defect that can intermittently cause the system to lock-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· GE Healthcare, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer - Product Usage: Is a Recalled by...

The Issue: Image acquisition failures and synchronization failure with the Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Medline Industries Inc

Recalled Item: NAMIC Stopcocks: (1) NAMIC STOPCOCK Recalled by Medline Industries Inc Due...

The Issue: Potential for sterile barrier breach. Microscopic pinholes within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is Recalled by...

The Issue: Image acquisition failures and synchronization failure with the Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Medline Industries Inc

Recalled Item: NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD Recalled by Medline...

The Issue: Potential for sterile barrier breach. Microscopic pinholes within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Johnson & Johnson Surgical Vision Inc

Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for...

The Issue: Nonconforming product was distributed in error. Product was nonconforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
FoodAugust 6, 2021· Ingredion

Recalled Item: Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with...

The Issue: Undeclared egg allergen

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2021· DuPont Nutrition USA, Inc

Recalled Item: Avicel Recalled by DuPont Nutrition USA, Inc Due to Out of specification...

The Issue: Out of specification results for conductivity.

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2021· Hikma Pharmaceuticals USA Inc.

Recalled Item: Bleomycin for Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Labeling: Not elsewhere classified: Mislabeling

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A800061 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A319416AM Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A800360 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing