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. 2,566 recalls have been distributed to Oklahoma in the last 12 months.
Showing 18361–18380 of 49,976 recalls
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACTIV.A.C Therapy System Recalled by KCI USA, INC. Due to The device may...
The Issue: The device may power off without notification to the user resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips M3015A Microstream CO2 Extension Model No. 862393 -used with...
The Issue: Affected M3015A extensions are incompatible with the lntelliVue X3 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lokomat Pro Recalled by Hocoma AG Due to The motor controller may fail,...
The Issue: The motor controller may fail, which can potentially lead to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: Recalled...
The Issue: A missing component (hand suction pump) in the emergency medical kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation" S7 System with Polaris Spectra Camera part number PSU...
The Issue: There is a potential for specific camera units to be affected by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component...
The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Core OneTouch Smart Cable Recalled by Verathon, Inc. Due to When...
The Issue: When video laryngoscopy system users apply, twisting motions while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 6mm implant component...
The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics,...
The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.