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. 1,050 recalls have been distributed to Oklahoma in the last 12 months.
Showing 17381–17400 of 49,976 recalls
Recalled Item: Nature-Throid 1 GR (65 mg) Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: CGMP deviations; repackaged product was recalled by the manufacturer because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...
The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diethylpropion Recalled by Calvin Scott & Company, Inc. Due to cMGP...
The Issue: cMGP Deviations: Drug products repackaged into pouches without supporting...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine Recalled by Calvin Scott & Company, Inc. Due to cMGP Deviations:...
The Issue: cMGP Deviations: Drug products repackaged into pouches without supporting...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diethylpropion Recalled by Calvin Scott & Company, Inc. Due to cMGP...
The Issue: cMGP Deviations: Drug products repackaged into pouches without supporting...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...
The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with 4mm Adapter - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650301018 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #65220955 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650301023 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Coils The MR Coil is intended to be used Recalled by Invivo Corporation...
The Issue: The labels have been mistakenly printed with an IPX1 rating symbol. IPX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.