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 101120 of 51,768 recalls

DrugJanuary 26, 2026· F.H. INVESTMENTS, Inc. (dba Asteria Health)

Recalled Item: ESTRADIOL Recalled by F.H. INVESTMENTS, Inc. (dba Asteria Health) Due to...

The Issue: Presence of Foreign substance - potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 26, 2026· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 B12 System Model Numbers:(1) 722067 Recalled by PHILIPS MEDICAL...

The Issue: Under certain conditions, the table may move unexpectedly when the Reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2026· Datascope Corp.

Recalled Item: CS100 IABP. Software Version CS100 IABP Q.01. Recalled by Datascope Corp....

The Issue: The firm has identified that the battery runtime and cycle specifications...

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

Class II — Potential Health HazardOngoing
FoodJanuary 23, 2026· Navitas, LLC.

Recalled Item: NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) Recalled by Navitas,...

The Issue: Potential contamination with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2026· Datascope Corp.

Recalled Item: CS300 IABP. Software Version CS300 IABP C.01. Recalled by Datascope Corp....

The Issue: The firm has identified that the battery runtime and cycle specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Auris Health, Inc

Recalled Item: MONARCH Platform Recalled by Auris Health, Inc Due to Device for...

The Issue: Device for bronchoscopic visualization, patient airway access has software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Stryker Corporation

Recalled Item: MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm...

The Issue: Due to a need to update the product labeling (Instructions for Use IFU) as a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2026· Agiliti Health - Ellis

Recalled Item: Adapt Pump Recalled by Agiliti Health - Ellis Due to Agiliti identified an...

The Issue: Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump)...

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

Class II — Potential Health HazardOngoing
DrugJanuary 21, 2026· Unichem Pharmaceuticals USA Inc.

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide tablets Recalled by Unichem...

The Issue: cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2026· Physio-Control, Inc.

Recalled Item: PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog...

The Issue: Due to pediatric defibrillator electrode delamination

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

Class II — Potential Health HazardOngoing
DrugJanuary 21, 2026· Unichem Pharmaceuticals USA Inc.

Recalled Item: Doxazosin Tablets Recalled by Unichem Pharmaceuticals USA Inc. Due to...

The Issue: Tablets/Capsules Imprinted with Wrong ID

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

Class III — Low RiskOngoing
Refund
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
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Green Guard Antiseptic Wipes (Benzalkonium Chloride 0.13%) Recalled by ACME...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%) Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Dukal BZK Antiseptic Towelette (Benzalkonium Chloride 0.13%) 1000 Packs per...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
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
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Medi-First Antiseptic Wipes (BZK)(Benzalkonium Chloride 0.13%) Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%) Recalled...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund