Product Recalls in New Mexico
Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,925 recalls have been distributed to New Mexico in the last 12 months.
Showing 15781–15800 of 27,850 recalls
Recalled Item: RS 5F DL XPP Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to A...
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 DL-55CM IR-145 Kit Non-Valved PG Recalled by Angiodynamics...
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 (Valved) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol...
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 IR-145 Kit Non-Valved with Nitinol GW PG Recalled by...
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 5F DL BIOFLO 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: 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: 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: 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: 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: 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: 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: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: The recalling firm has identified two lots of test strips that are out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: The recalling firm has identified two lots of test strips that are out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: The recalling firm identified four US lots of test strips out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...
The Issue: Potential for positively biased results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.