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. 1,965 recalls have been distributed to Washington in the last 12 months.
Showing 19061–19080 of 29,208 recalls
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics notified customers that errors were contained in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...
The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYFRECATOR 2000 HANDPIECE SHEATH Recalled by ConMed Corporation Due to For...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.