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. 2,629 recalls have been distributed to Washington in the last 12 months.
Showing 27321–27340 of 51,768 recalls
Recalled Item: Tibial 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.
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.
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.
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.
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.
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.
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.
Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - 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.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm...
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: BOX KIT1171C KIT LAP CYSTECTOMY 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.
Recalled Item: Endo GIA" 45mm Gray Curved Tip Articulating Vascular Reload with 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.
Recalled Item: Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with 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.