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. 2,681 recalls have been distributed to Oklahoma in the last 12 months.
Showing 861–880 of 28,654 recalls
Recalled Item: Portrait VSM Model nos. 6660000-666 Monitor Recalled by GE Healthcare...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carescape B450 Recalled by GE Healthcare Finland Oy Due to Potential loss of...
The Issue: Potential loss of monitoring on affected monitors when powered by certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator 11mm. Cranial Perforator. Recalled by Integra...
The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...
The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...
The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...
The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...
The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Microbiology Data Management System Recalled by Becton...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.