State
73,741 recalls have nationwide distribution and so reach New Mexico. 3,636 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,636 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 815 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,636 recalls whose distribution notice names New Mexico specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mylan Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to an out-of-specification result for an unknown impurity.
Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.
American Health Packaging is recalling Lamivudine Tablets due to an error in the package insert that incorrectly lists tablet description coding.
Contract Manufacturer is recalling specific CM truck bed models because attachment brackets may crack, potentially causing the bed to shift or detach.
McNeilus is recalling 330 CNG-powered trucks from 2013-2018 because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.
Hyundai Translead is recalling 2017-2018 Duralite HT flatbed trailers because bulkhead brackets may break, causing the bulkhead to detach and create a road hazard.
Terex is recalling 2016-2017 TLM aerial devices because an incorrect holding valve may cause the boom to drift down if a hose bursts.
TransPower is recalling 2017-2018 Peterbilt 579 electric trucks because they lack required Electronic Stability Control systems, increasing crash risk.
Humanscale is recalling QuickStand Lite workstations because the adjustable arm can break and fall, posing a risk of injury to consumers.
Airstream is recalling specific 2016-2017 Flying Cloud and International trailers because an inverter may contact a fuse, creating a fire hazard.
General Motors is recalling 2015-2018 Chevrolet Trax vehicles because a front lower control arm joint may be improperly welded, posing a crash risk.
Toyota is recalling 2020 Supra vehicles because the driver's seat belt guide loop mount may be improperly welded, which could compromise restraint in a crash.
Nissan is recalling 2018-2019 Nissan and Infiniti vehicles because backup camera settings can be adjusted to hide the rear view image, increasing crash risk.
Chrysler is recalling specific Mopar replacement passenger air bag modules that did not complete developmental testing. These modules may not perform as designed in a crash, increasing injury risk.
OMNIlife science Inc. is recalling six ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.
OMNIlife science Inc. is recalling 14 ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.
Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111W units because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.
OMNIlife science Inc. is recalling 22 ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.
Keystone is recalling 2020 Cougar 30RKD trailers because emergency exit windows lack red handles and labels, potentially delaying evacuation during an emergency.
Siemens Medical Solutions is recalling syngo.CT software version VA48A_SP5.5 for specific SOMATOM CT models due to scanning workflow interruptions and unexpected user notifications.
Integra LifeSciences Corp. is recalling 237 units of the Jarit GEMINI CLAMP because a small crack may cause corrosion and breakage after repeated sterilization.
Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111Z devices because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.
Ford is recalling 2017 Ford Explorer vehicles with power front seats because the seat frames may have sharp edges that could injure occupants.
Heidelberg Engineering is recalling 29 SPECTRALIS ophthalmic imaging devices because a software configuration error may cause incorrect display of patient master data.
Fujifilm is recalling 174 FDR Go Plus mobile X-ray systems because a graphics driver issue may cause the device to display a Blue Screen of Death.