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. 1,038 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,038 in last 12 months

Showing 27321–27340 of 51,768 recalls

Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Roche Diagnostics Corporation

Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...

The Issue: The device may give a falsely elevated result that is non-reproducible. If...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
DrugApril 27, 2018· Sanofi-Aventis U.S. LLC

Recalled Item: Docetaxel injection concentrate Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Superpotent drug: over-concentrated vials of Docetaxel injection concentrate...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Riomet (metformin hydrochloride oral solution) Recalled by Sun...

The Issue: Labeling: Not Elsewhere Classified: Sun Pharma has decided to initiate this...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VWR ZESTAW DO VATS KLIN Product Usage: The Endo Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX PST03533 KIT APP STAPLER Product Usage: The Endo GIA Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VMIN ZESTAW DO VATS PODSTAWOWY Product Usage: The Endo Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX PST03699 KIT APP MED ALTERNATIV STAP Product Usage: The Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX LAPZD ZESTAW DO SG (2) BOX LAPISG1 ZESTAW Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)KIT4184 APEN LOBECTOMY KIT X0 Item Number: KIT4184 APEN LOBECTOMY...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX HEMIGX1 ZESTAW DO HEMICOLECTOMII (Item Number HEMIGX1 ZESTAW DO...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX TGGLOGOWX1 DO TOTAL GASTRECTOMIII Product Usage: The Endo GIA Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: KIT-DE-0080 BYPASS KIT LOHNE X1( Item KIT-DE-0080) Product Usage: The...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· Draeger Medical, Inc.

Recalled Item: Carina Ventilator Recalled by Draeger Medical, Inc. Due to The valve...

The Issue: The valve assembly material may become corroded due to insufficient cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX KITDE0143 BYPASS BOX (Item Number: KITDE0143 Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing