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. 2,840 recalls have been distributed to Washington in the last 12 months.
Showing 1381–1400 of 29,208 recalls
Recalled Item: Orascoptic Superior Visualization Custom loupes configured with Phantom...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L17-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C10-3v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Phantom Essential kit ( Nose pad Recalled...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S8-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S12-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare OEC 9800. Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare OEC 9900 Elite C-arm Systems. Recalled by GE Medical Systems,...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sparrow Ascent Patient Controller Recalled by Spark Biomedical Inc Due to...
The Issue: Due to manufacturing issue, neurostimulator device may experience "cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SmartPump Tourniquet Recalled by Stryker Corporation Due to...
The Issue: Tourniquet cuff flange may become detached from the bladder. If leak occurs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) Recalled by North American Rescue...
The Issue: Device used for unilateral or bilateral occlusion of blood flow to the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 3.0T Quasar Dual Model Number (REF): 781150 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.