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 16421–16440 of 28,654 recalls
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU Recalled by Ace...
The Issue: The product inside the package is incorrect. A single blade shoe was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due to Firm is...
The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ratcheting Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due...
The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Functionality in the report sections "Findings Information" and "Summary of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use...
The Issue: Urea Nitrogen reagent kit demonstrated an increased incidence of Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...
The Issue: These one-way valves may disconnect at the joint between the two components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDim Eleva 708032 As a multifunctional universal imaging application...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional...
The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.