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. 1,009 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26621–26640 of 49,976 recalls
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.75% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Signature Care Calcium Chews Recalled by Bestco, Inc. Due to A packaging...
The Issue: A packaging revision and lack of revision to the corresponding packaging...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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: 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: 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: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER MicroScan MICroSTREP Plus Panel Recalled by Beckman Coulter...
The Issue: Beckman Coulter has received customer complaints of lowered minimum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...
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 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.
Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...
The Issue: Use of the product with insufficient lubrication may prolong surgery due to...
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: 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: 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: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: Potential failure of sterile packaging seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.