Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 27061–27080 of 52,000 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: CAN 5F SINGLE XCELA PICC 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: 5F DL BIOFLO PASV 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: BioFlo PICC (NV) 5FSL-55cm Maximal Barrier Nursing Kit w/ 70cm Nitinol Wire...
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: 5F DL BIOFLO PICC 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: 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: RS TANDEM 5F DL XPP 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: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...
The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...
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: 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: 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: 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: 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: 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: 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: 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 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: 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: Preferred Plus Pharmacy Antacid (Aluminum Hydroxide 200mg 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.