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. 2,765 recalls have been distributed to Washington in the last 12 months.
Showing 13241–13260 of 29,208 recalls
Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...
The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cautery Tip Cleaner Product Usage: electrosurgical accessory Recalled by...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...
The Issue: Incomplete seal and premature expiration of individually packaged Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE TITANIUM NON- FILLED Recalled by Angiodynamics Inc....
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.