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. 2,647 recalls have been distributed to Oklahoma in the last 12 months.
Showing 6801–6820 of 49,976 recalls
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules USP Recalled by Amerisource Health Services LLC Due to...
The Issue: Failed Impurities/Degradation Specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vasostrict (vasopressin in 5% Dextrose) Injection Recalled by Par Sterile...
The Issue: Superpotent Drug: Assay from the 3-month and 6-month stability intervals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...
The Issue: European version of microcatheter were distributed within US which contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...
The Issue: European version of microcatheter were distributed within US which contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023 Recalled by Brasseler...
The Issue: The device has a grip detail (right angle latch) out of specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...
The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...
The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.