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. 2,719 recalls have been distributed to Washington in the last 12 months.
Showing 20301–20320 of 51,768 recalls
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...
The Issue: A mix-up of autosampler tube positions with a possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermage Face Tip 3.0 Recalled by Solta Medical Inc Due to Complaints of...
The Issue: Complaints of sparking of the tips of the electrosurgical device used in RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron Recalled by Philips North America, LLC Due to...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Eleva Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Eleva System codes 708028 708027 Recalled by Philips North...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 15 & 12 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poly G Integris H5000 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 Recalled by Philips North America, LLC Due to A capacitor inside...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Exper FD Series. System codes 722003 722010 722022 722005 Recalled by...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: Recalled by Smith &...
The Issue: Due to a potential for sterile barrier breach. A complaint was received that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dawson-Mueller Drainage Catheter Recalled by Cook Inc. Due to Specific lots...
The Issue: Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: Chemical contamination; out of specification results obtained for equipment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.