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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.
Showing 2141–2160 of 49,976 recalls
Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...
The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base Recalled...
The Issue: Engaging titanium base was manufactured 180 degrees around the post from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FARAWAVE 1.0 Pulsed Field Ablation Catheter Recalled by Boston Scientific...
The Issue: The potentially impacted units were manufactured using specific equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 800 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 600 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxI 600 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxI 800 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....
The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...
The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...
The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...
The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...
The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...
The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Granules...
The Issue: Failed Dissolution Specifications: Product failed to meet dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Blood Products Administration Set Dual-Inlet Recalled by Fresenius Kabi...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PILLAR SA Ti Recalled by Orthofix U.S. LLC Due to A 37 mm implant width...
The Issue: A 37 mm implant width intervertebral body fusion device has a labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Potential for external cassette leaks
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.