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. 2,432 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,432 in last 12 months

Showing 5138151400 of 51,768 recalls

Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Infusion Pump Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2012· Orthosensor

Recalled Item: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass...

The Issue: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface...

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

Class II — Potential Health HazardOngoing
DrugFebruary 3, 2012· Lloyd Inc

Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 1, 2012· Roche Molecular Systems, Inc.

Recalled Item: COBAS AmpliPrep Sample Tube Input Barcode Clips Recalled by Roche Molecular...

The Issue: Certain lots of COBAS AmpliPrep (CAP) S-tube Input (Box of 12 bags 12x24...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2012· Beckman Coulter Inc.

Recalled Item: IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent Recalled by...

The Issue: The recall was initiated because Beckman Coulter has confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH...

The Issue: Stryker has become aware that there exists a potential for breach of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2012· Exactech, Inc.

Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...

The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2012· GE Healthcare, LLC

Recalled Item: VMX Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware of...

The Issue: GE Healthcare has become aware of an issue associated with the base casting...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2012· Beckman Coulter Inc.

Recalled Item: COULTER PrepPlus Recalled by Beckman Coulter Inc. Due to The recall was...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing