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 7661–7680 of 49,976 recalls
Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Product Code 6802445 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Product Code 6802413 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Product Code 6802783 and Product...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stay Safe Cap Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Updating the labeling to include additional warnings and contraindications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP Emergency Drive Recalled by Maquet Medical Systems USA Due to...
The Issue: Product removal due to possible blocking or impairment of the CARDIOHELP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stabilyze Sugar Stable Dark Chocolate Peanut Butter Recalled by Betty Lou's...
The Issue: Undeclared Sesame
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to This recall is...
The Issue: This recall is part of a 2-issue recall for the same system. When using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.