Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,642 recalls have been distributed to Oklahoma in the last 12 months.
Showing 8101–8120 of 28,654 recalls
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: Alcon Clareon IOL with AutonoMe Delivery System Recalled by Alcon...
The Issue: Due to device (preloaded intraocular lens) mislabeling, associated with...
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.
Recalled Item: BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) Recalled by Becton...
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.