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. 2,465 recalls have been distributed to Oklahoma in the last 12 months.
Showing 33161–33180 of 49,976 recalls
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...
The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...
The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...
The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...
The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra External Fixation System Rocker Bottom Model # 12225400. For...
The Issue: The silicone insert embedded in the rocker bottom has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...
The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...
The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection Recalled by...
The Issue: Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.