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 15521–15540 of 27,850 recalls
Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...
The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...
The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 16FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensor Foley catheter 10FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 18FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 8FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 12FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.