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 8701–8720 of 28,654 recalls
Recalled Item: RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated Recalled by Collagen...
The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OER-Elite Endoscope Reprocessor-for use in cleaning and high-level...
The Issue: The detergent and alcohol tank tubing may have been incorrectly assembled in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EnPlace is a single use trans-vaginal pelvic floor repair Recalled by...
The Issue: Certain lots may not have been packaged wth the Channel Tube Limiter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products VersaTips Recalled by Ortho-Clinical Diagnostics,...
The Issue: The lot has a shape deformity which may lead to a 16% reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERAKOS CELLEX Photopheresis Procedural Kit Recalled by Mallinckrodt...
The Issue: This recall was initiated to recover a Dunnage Case, which is a case of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaporizer Sevoflurane Maquet Filling Recalled by Getinge Usa Sales Inc Due...
The Issue: A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray...
The Issue: Potential safety issue under specific preconditons that may result in a user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...
The Issue: The chrome surface of the push brace can crack during use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...
The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.