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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.
Showing 7341–7360 of 49,976 recalls
Recalled Item: EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 48IN (121.9CM) INJ LINE ROTATING ADAPT (900psi) Recalled by Smiths Medical...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 20IN (50.8CM) INJ LINE ROTATING ADAPT Recalled by Smiths Medical Asd...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1050 STOPCOCK LEFT ROTATOR OFF HANDLE Recalled by Smiths Medical Asd Inc Due...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR WITH MALE LUER LOCK Recalled by Smiths Medical Asd Inc...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6IN PRESSURE TUBING Recalled by Smiths Medical Asd Inc Due to There is a...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK Recalled by Smiths Medical Asd...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex LOGICAL CATH LAB KIT Recalled by Smiths Medical Asd Inc Due to There...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medex 700PSI STOPCOCK W/ROTATOR Recalled by Smiths Medical Asd Inc Due to...
The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated...
The Issue: Due to incorrect product/device within packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHENYLephrine HCl 5000 mcg/50 mL in 0.9% Sodium Chloride Injection Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: labetalol HCl 20 mg/4mL Injection Recalled by SCA Pharmaceuticals, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl 30 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 40 mg in 0.9% Sodium Chloride Injection Recalled by SCA...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.