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. 936 recalls have been distributed to Oklahoma in the last 12 months.
Showing 46141–46160 of 49,976 recalls
Recalled Item: Nimodipine Capsules 30 mg Recalled by Sun Pharmaceutical Industries Inc. Due...
The Issue: Crystallization; crystallized nimodipine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Sandoz Incorporated Due to Presence of...
The Issue: Presence of Particulate Matter: Found during examination of retention samples.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XIYOUJI QINGZHI CAPSULE Recalled by Dolphin Intertrade Corporation Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: JaDera Recalled by Dolphin Intertrade Corporation Due to Undeclared Sibutramine
The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate; lot being recalled as a precaution due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...
The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...
The Issue: There is a possibility that the pump head was not shipped in the locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...
The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunny Sea Sardines in Tomato Sauce Recalled by Golden Beach Inc Due to...
The Issue: Golden Beach Inc. is recalling Sunny Sea Sardines in Tomato Sauce for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...
The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...
The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....
The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS System (PST) The CoaguChek XS PT test strips Recalled by Roche...
The Issue: Roche has confirmed the potential for an undetected elevated INR test result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...
The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.