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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.
Showing 26241–26260 of 49,976 recalls
Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved PG Recalled by Angiodynamics Inc....
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS 5F DL XCELA PICC Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical Inc.)...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAN 5F DL BIOFLO PASV PICC NURSING TRAY Recalled by Angiodynamics Inc....
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS TANDEM 5F DL BIOFLO PASV Recalled by Angiodynamics Inc. (Navilyst Medical...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG Recalled...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS - TANDEM 5F DL BIOFLO MIDLINE Recalled by Angiodynamics Inc. (Navilyst...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS 5F DL XPP KIT Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due...
The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PHYT Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: There is a potential for imprecise results when using the slides. Increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS-7 Recalled by Konica Minolta Medical Imaging USA, Inc. Due to Panasonic...
The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Recalled by Konica Minolta Medical Imaging USA, Inc. Due to...
The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...
The Issue: In certain eyepiece configurations the laser shutter may not close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: The firm will be updating the Instructions for Use for the product. Current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...
The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...
The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...
The Issue: Stryker Sustainability Solutions has received an increase in reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: The firm will be updating the Instructions for Use for the product. Current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Inc. Due to...
The Issue: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Inc. Due to...
The Issue: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RPC Children's Non-Aspirin (Acetaminophen 160 mg) Elixir Recalled by RIJ...
The Issue: CGMP Deviations: Products are being recalled due to an out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.