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. 1,872 recalls have been distributed to New Mexico in the last 12 months.
Showing 19681–19700 of 27,850 recalls
Recalled Item: Crit Line in a Clip (CLiC). CliC P/N: CL 10041001 Recalled by Fresenius...
The Issue: Use of the Blood Pressure Graph located on the Crit-Line screen of the 2008T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickSlide MGS-80 Recalled by Hardy Diagnostics Due to Discrepant culture...
The Issue: Discrepant culture and gram stain results, which could potentially lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 EverFiex" Self-expanding Peripheral Stent System Recalled by Ev3, Inc....
The Issue: Medtronic is issuing a medical device recall to return product potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Right Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...
The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz....
The Issue: Product did not meet specifications for Zinc Acetate (OOS).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...
The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...
The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.