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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 30661–30680 of 49,976 recalls
Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...
The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ATENOLOL Tablets Recalled by Legacy Pharmaceutical Packaging LLC Due to...
The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adalat CC (nifedipine) Extended Release Tablets 30 mg Recalled by Alvogen,...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adalat CC (nifedipine) Extended Release Tablets Recalled by Alvogen, Inc Due...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RIVASTIGMINE Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Cross-contamination with other products -Related Substances test for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sensodyne Repair & Protect Whitening Recalled by GSK Consumer Healthcare Due...
The Issue: Presence of Foreign Substance; low concentration of an additional flavoring...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software changes now available to address several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...
The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software changes now available to address several issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.