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. 2,443 recalls have been distributed to Oklahoma in the last 12 months.
Showing 36541–36560 of 49,976 recalls
Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...
The Issue: Chemical Contamination: The product may contain trace amounts of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....
The Issue: Chemical Contamination: The product may contain trace amounts of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Traditional Round Yellow Tortillas. Sold under the brand names of: Better...
The Issue: Firm was notified by a customer that the product contained an undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...
The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...
The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...
The Issue: The firm is conducting a product correction due to an increase in U90-382 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cetirizine HCl 10 mg Tablet Recalled by Perrigo Company PLC Due to Failed...
The Issue: Failed Impurity/Degradations Specifications; impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Actavis...
The Issue: Failed Dissolution Specifications: Low Out-of-Specification results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.