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. 2,798 recalls have been distributed to Washington in the last 12 months.
Showing 9001–9020 of 29,208 recalls
Recalled Item: Affected components are limited to the Monoprice charging cable (Product...
The Issue: Warning Added: Using damaged cables or chargers, or charging when moisture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147...
The Issue: Due to an increased risk of false positive Acinetobacter calcoaceticus-...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant 3.5x10 Recalled by Jjgc Industria E Comercio De...
The Issue: 3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261....
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Crescent Knife Recalled by Beaver Visitec International, Inc....
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle Recalled by Cook Inc. Due to Transseptal needles may...
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComposiTCP 30 Interference screw D 7- L:25 mm Recalled by SCIENCE & BIO...
The Issue: Mislabeled product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Electrodes Recalled by 3M Company - Health Care Business Due to...
The Issue: Potential for breakage of the ECG electrode carbon stud from the eyelet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis/ Sensis Vibe systems with software VD1X as follows: (1)Sensis...
The Issue: System operator manual states that the system should be rebooted once, every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE...
The Issue: Due to component (housing and plunger) detaching from the semi-automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliquid MD version 3.4 software used in conjunction with Analyst Recalled by...
The Issue: The values of the Internal Standard (IS) concentrations are incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellume COVID-19 Home Test Recalled by ELLUME LTD Due to Due to a higher rate...
The Issue: Due to a higher rate of false positive test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.020 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.