State
73,809 recalls have nationwide distribution and so reach New Mexico. 3,638 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,638 recalls naming New Mexico we have scored against our rubric, 745 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 816 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,638 recalls whose distribution notice names New Mexico specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
OriGen Biomedical is recalling 72 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of tube disconnection from the hub caused by adhesive failure.
OriGen Biomedical is recalling 66 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of the clear tube disconnecting from the hub if clamped improperly.
OriGen Biomedical is recalling 145 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of the clear tube disconnecting from the hub.
OriGen Biomedical is recalling 66 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of the clear tube disconnecting from the hub.
Maquet Cardiovascular is recalling Getinge Meera Mobile Operating Tables because exposed electronic components may cause electric shock to users.
Porsche is recalling specific Cayenne and Panamera models because a degraded bushing may allow the driver to exit the vehicle while the transmission is not in Park, increasing crash risk.
Icco Cheese Co Inc is recalling Gia Russa Whole Grain Italian Unseasoned Bread Crumbs because the product contains undeclared walnuts and pecans.
OriGen Biomedical is recalling 61 units of ECMO Reinforced Dual Lumen Cannulas due to a risk of tube disconnection from the hub caused by adhesive failure.
Flowonix Medical Inc is recalling 6,445 Prometra II Programmable Pumps because a software defect can cause the device to shut down unexpectedly.
Hayward Industries is recalling specific pool heater vent kits because improper sizing may allow carbon monoxide leaks. Consumers should stop using affected heaters and contact the company for a free replacement.
OMNIlife science Inc. is recalling 9 OMNIBotics iBlock Cutting Guides because they may not lock onto the iBlock Saw Guide as intended and could loosen during use.
Leica Microsystems is recalling 17,179 cryostats because the labels lack warnings about the fire risk associated with flammable freezing sprays.
Zimmer Biomet is recalling 15 Oxford Partial Knee drill guides because incorrect raw materials may cause the screw component to corrode.
Flowonix Medical Inc. is recalling 163 Prometra II Programmable Pumps due to a software defect that can cause unexpected shutdowns.
Centurion Medical Products Corporation is recalling sterile nail nippers because the sterile barrier pouch seal is compromised, potentially affecting sterility.
Bio-Rad Laboratories is recalling MRSASelect II diagnostic plates due to abnormal agar coloration and non-characteristic colony growth. The recall covers 3,632 units distributed nationwide.
Philips is recalling IntelliVue MX40 Patient Monitors because they may experience increased power consumption and lack visual or audible notifications when in a low battery state.
Zimmer Biomet is recalling 3 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw materials may cause corrosion.
Stryker is recalling High Flow II Tube Sets because they consistently leak and detach from the cassette. The product is a medical device accessory distributed nationwide and internationally.
AngioDynamics is recalling 178 Solero Microwave Tissue Ablation System generators to update manuals and software, reducing the risk of patient harm from procedure delays.
Flowonix Medical Inc is recalling Prometra Clinician Programmer software due to a defect that can cause intrathecal pumps to shut down unexpectedly.
Zimmer Biomet is recalling 10 units of Oxford Partial Knee Phase 3 Femoral Drill Guides because incorrect raw material was used, potentially leading to corrosion.
Philips is recalling IntelliVue MX40 Patient Monitors because they may fail to provide visual or audible alerts when the battery is low.
AngioDynamics is recalling Solero Microwave Tissue Ablation System applicators to reduce the risk of patient harm from delayed procedures via manual and software updates.
Philips is recalling IntelliVue MX40 Patient Monitors because they may consume excess power and fail to provide visual or audible low-battery alerts.