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. 2,766 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,766 in last 12 months

Showing 1386113880 of 51,768 recalls

Medical DeviceJanuary 28, 2022· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS Recalled by Remote Diagnostic Technologies Ltd. Due to...

The Issue: Distribution of Defibrillators that are not approved or cleared for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material #...

The Issue: Dimension Vista Magnesium Flex reagent cartridge lots exhibiting imprecision...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· Sam Medical Products

Recalled Item: SAM CHEST SEAL Combo LOT Y060321-09 Recalled by Sam Medical Products Due to...

The Issue: Due to partially assembled valved dressing that has a hole within it instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated)...

The Issue: If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· Brasseler USA, Medical L.L.C.

Recalled Item: Brasseler USA Recalled by Brasseler USA, Medical L.L.C. Due to One lot of...

The Issue: One lot of product was distributed in unsealed packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Integrity Implants Inc.

Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...

The Issue: Potential for weld separation of the Upper Tulip Head component from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Integrity Implants Inc.

Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...

The Issue: Potential for weld separation of the Upper Tulip Head component from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Integrity Implants Inc.

Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...

The Issue: Potential for weld separation of the Upper Tulip Head component from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· IN MY BATHROOM LLC

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Medtronic MiniMed

Recalled Item: MiniMed 630G: MMT-1715 Recalled by Medtronic MiniMed Due to New or...

The Issue: New or replacement insulin pumps are not pre-programmed with basal rates or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Hologic, Inc

Recalled Item: Panther Fusion Extraction Reagent-X Recalled by Hologic, Inc Due to Failed...

The Issue: Failed stability specifications for reagent kits that may result in false...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· C.R. Bard Inc

Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...

The Issue: There is a potential to leak from the catheter where it connects to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· C.R. Bard Inc

Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...

The Issue: There is a potential to leak from the catheter where it connects to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· E25Bio, Inc.

Recalled Item: E25Bio COVID-19 Direct Antigen Rapid Test Recalled by E25Bio, Inc. Due to...

The Issue: The Test is not authorized, cleared, or approved by FDA for clinical...

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

Class I — Serious Health HazardOngoing
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Enoxaparin Sodium Injection Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: RIVASTIGMINE TRANSDERMAL SYSTEM Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: ARMOUR THYROID (thyroid tablets Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Donepezil HCl Tablets Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: SPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Warfarin Sodium Tablets Recalled by CARDINAL HEALTHCARE Due to CGMP...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund