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. 2,592 recalls have been distributed to Oklahoma in the last 12 months.
Showing 14441–14460 of 49,976 recalls
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Delivery System Recalled by Baxter Healthcare Corporation Due...
The Issue: If the operator initiates therapy with a saved prescription profile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage Recalled by Revive...
The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artesunate for Injection Recalled by AMIVAS (US), LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Air filter failed post integrity test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES Recalled by O&M...
The Issue: All lots of the glove may discolor and lose elasticity upon aging, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...
The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...
The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.