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. 2,824 recalls have been distributed to Washington in the last 12 months.
Showing 4141–4160 of 29,208 recalls
Recalled Item: Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX...
The Issue: Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE Recalled by MEDLINE...
The Issue: It has been identified that testing documentation does not support that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX and Patient Information Center iX Expand...
The Issue: Event Catalog information does not save when copied and transferred from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro2 Guidewires are a steerable guidewire family with a Recalled by...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...
The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro SELECT Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro Neuro Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...
The Issue: The required leakage test was not performed following of a re-work for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...
The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syntel Silicone Thrombectomy Catheter Recalled by LeMaitre Vascular, Inc....
The Issue: The guide tip can become damaged and result in the tip detaching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial access kit (without Prep solutions) Bit and Guard- Recalled...
The Issue: Potential holes and tears in the sterile packaging (header bag) of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in....
The Issue: Potential contamination of the product with latex adhesive residual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Inspection System Recalled by YAMAHA MOTOR CORPORATION Due to...
The Issue: Non-medical laser products which were determined to not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelli-C: Right side suspended Tabletop Recalled by NRT X-RAY A/S Due to...
The Issue: X-ray system C-arm may experience uncontrolled motion if 1) AC motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yamaha Surface Mounter YR series Recalled by YAMAHA MOTOR CORPORATION Due to...
The Issue: Non-medical laser products which were determined to not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes labeled as: a) SYR 10ML L/L CONTROL Recalled by MEDLINE INDUSTRIES,...
The Issue: These syringes were identified to be affected by the FDA Safety Alert issued...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.