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 33041–33060 of 49,976 recalls
Recalled Item: cobas 6800/8800 system Hepatitis Viral B DNA Detection Product Usage:...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Four Birthing Bed Model P3700 The primary packaging is Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The...
The Issue: Topcon discovered an anomaly with titration, only when EpM is turned on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that a change to an Order Set will not be saved in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poppers brand Mozzarella Cheese Sticks Net Wt. 32 oz. (2 Recalled by...
The Issue: Monogram Appetizers is recalling Poppers Brand Mozzarella Cheese Sticks...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...
The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trokendi XR (topiramate) extended-release capsule Recalled by Supernus...
The Issue: Superpotent Drug: Failure of assay specifications in the capsule.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta...
The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fire roasted Poblano & Jalapeno popper bites packaged in a Recalled by...
The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...
The Issue: Software malfunction; The action being taken due to the device becoming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.