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. 2,379 recalls have been distributed to Oklahoma in the last 12 months.
Showing 46801–46820 of 49,976 recalls
Recalled Item: Atropine Injection Recalled by Pallimed Solutions Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate/Testosterone Enanthate Injection Recalled by Pallimed...
The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injectable Recalled by Pallimed Solutions Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIC with B6 and B12 Recalled by Pallimed Solutions Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Some of the KWIK-STIK...
The Issue: Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taco Seasoning Recalled by Decoty Coffee Company, Inc Due to Undeclared...
The Issue: Recently, DeCoty Taco Seasoning, 1.25 lb (Lot numbers 010111-021313) and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin) Recalled...
The Issue: Use of affected lots may give false indication of susceptibility to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon Femoral Distal Augment- Left Recalled by...
The Issue: Stryker Orthopaedics received a report that a label on the external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Broken tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...
The Issue: Failed Tablet/Capsule Specifications: Broken tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg Recalled by...
The Issue: Failed USP Dissolution Test Requirements: Out-of-specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner & Reprocessor System Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) has determined that a limited number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511...
The Issue: Medtronic is recalling the Medtronic Paradigm Insulin Pump because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.