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. 2,844 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,844 in last 12 months

Showing 141160 of 51,768 recalls

Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Roche Diagnostics Operations, Inc.

Recalled Item: cobas pro integrated solutions with cobas c 503 analytical units: Recalled...

The Issue: Software defect, which allows the system to accept erroneous, non-monotonous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2026· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Private Label CVS. Model Number: CVS405406. Helps maintain a moist Recalled...

The Issue: Potential packaging failures, which could lead to a breach in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for Recalled...

The Issue: Issue with software algorithm which may lead to overpressure events.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus High Flow Insufflation Unit. Model Number: UHI. Used for Recalled by...

The Issue: Issue with software algorithm which may lead to overpressure events.

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

Class I — Serious Health HazardOngoing
DrugJanuary 16, 2026· Specialty Process Labs LLC

Recalled Item: Thyroid Recalled by Specialty Process Labs LLC Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2026· GE Healthcare

Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Client Recalled by...

The Issue: Under certain workflows, patient information shown in the viewer may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2026· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1)...

The Issue: Potential packaging failures, which could lead to a breach in the sterile...

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

Class II — Potential Health HazardOngoing