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. 2,610 recalls have been distributed to Oklahoma in the last 12 months.
Showing 12301–12320 of 28,654 recalls
Recalled Item: DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Recalled by Ra...
The Issue: A software issue was identified which could result in user or patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Canister System (finished part numbers FG 12009 Recalled by Stryker...
The Issue: Some Canister Scanning Labels used to calibrate the Triton Canister System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical, Cardiac Rhythm Management Division Due...
The Issue: Past updates to programmers and transmitters may lead some implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS REV F TIBIA OFFSET CEMENTED Recalled by Aesculap Implant Systems...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Detect Cotinine Recalled by Polymer Technology Systems, Inc. Due to The...
The Issue: The firm is removing the product from the market after discussions with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...
The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LabPro Data Management System Recalled by Beckman Coulter Inc. Due to A...
The Issue: A security-only update was released via remote diagnostics on January 14,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...
The Issue: The action is being taken due to an increase in complaints relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection...
The Issue: Potential for the sterile barrier to be compromised. Products with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...
The Issue: The action is being taken due to an increase in complaints relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COHERENCE Oncologist Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue arises when an offset calculation is followed by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth...
The Issue: The catheter locks for the lot may contain an 8Fr catheter lock instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.