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. 1,918 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,918 in last 12 months

Showing 2714127160 of 29,208 recalls

Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14217-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14200-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14211-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14207-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14206-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products-HCY Reagent packaged in a kit carton. Catalog#...

The Issue: The firm is recalling the specific lot due to lower than expected results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ 4800 system z480 instrument. Integrates fully automated total...

The Issue: In rare instances, channel shifted results have been generated with cobas¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Fresenius Medical Care Holdings, Inc. dba Renal Solutions

Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...

The Issue: Product is being recalled because the combination of the current 50 mg vial,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2013· Hospira Inc.

Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...

The Issue: It was discovered that there was a potential for the piercing pin on certain...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2013· Sysmex America, Inc.

Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...

The Issue: The current Century Break patch did not contain the same setting for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2013· Cordis Corporation

Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...

The Issue: Correction to provide clarification and additional labeling to minimize...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Stylet Product...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Helistat Absorbable Hemostatic Recalled by Integra LifeSciences Corporation...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: HeliPlug Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Custom Spine, Inc.

Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...

The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: CollaPlug Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing