Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 7961–7980 of 27,451 recalls
Recalled Item: Dimension LTNI -In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension CTNI-In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 Recalled by...
The Issue: There is a potential for sporadic incidents of positive and negative biases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: #1 MAC F/O LARYNGOSCOPE Recalled by Baxter Healthcare Corporation Due to...
The Issue: Packaging error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager SafeStar 55 Recalled by Draeger Medical, Inc. Due to Possible...
The Issue: Possible occlusion of filters due to manufacturing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...
The Issue: The outer package is mislabeled and the package contains a different IOL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...
The Issue: The affected staplers have the potential for the staple guide to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Central Station (CSCS) V2 Recalled by GE Healthcare, LLC Due to...
The Issue: The CARESAPE Central Station (CSCS) V2 can shut down due to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) Recalled by...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Recalled by...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS) Recalled by...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta" Plus3 White Blend OEM (sterile Recalled by Becton Dickinson &...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.