State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Merit Medical Systems is recalling 15 Custom Sheath Introducer Kits because they were incorrectly labeled and contained the wrong sheath assembly.
ICU Medical is recalling 10 Central Venous Catheters because the included guidewire cannot pass through the needles.
Bard Peripheral Vascular Inc is recalling 200 units of PowerPort ClearVUE Slim Implantable Ports because the catheter locks may be 8Fr instead of the labeled 6Fr.
ICU Medical is recalling 60 units of Model 41406-23 Central Venous Catheters because the included guidewires cannot pass through the needles.
Edwards Lifesciences is recalling 35 HemoSphere oximetry cables due to intermittent communication caused by inconsistent crimping of connectors.
C.R. Bard is recalling 8,392 SureStep Foley Tray Systems because a white paper-type residue may be attached to the catheter.
ICU Medical is recalling 15 units of Central Venous Catheters because the included guidewire cannot pass through the needles.
ICU Medical is recalling 10 Central Venous Catheters because the included guidewire cannot pass through the needles. The defect prevents proper use of the device.
ICU Medical is recalling 235 Central Venous Catheters because the included guidewire cannot pass through the needles.
Becton, Dickinson and Company is recalling 1,473 vials of Analyte specific reagent (CD45) because of false positive reactions. The product is used for in vitro diagnostic testing.
ICU Medical is recalling 260 units of Central Venous Catheters because the included guidewire cannot pass through the needles.
ICU Medical is recalling 20 Central Venous Catheters because the included guidewire cannot pass through the needles. The product was distributed to US consignees and Canada.
Ra Medical Systems is recalling DABRA catheters because the actual shelf life is shorter than labeled, potentially causing calibration failures.
Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.
Genicon is recalling 1,550 units of the EZee Single Use Specimen Retrieval Bag to provide updated labeling instructions for multiple specimen retrieval.
Cardiac Assist, Inc. is recalling five TandemHeart pump kits because an assembly error may prevent the device from priming.
Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.
Medtronic is recalling 83 Vertex Select Multi Axial Screws because the product length is shorter than labeled. The recall covers units distributed in California and Michigan.
Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Very Berry due to observed separation in the secondary packaging.
Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Pretty in Pink due to observed separation in the secondary packaging.
Glaxosmithkline is recalling 288 packages of ChapStick Total Hydration Moisture Tint Peachy Keen due to observed separation in the secondary packaging.
Altec is recalling 2018-2020 aerial devices and digger derricks because bolts securing the pedestal to the turntable may fail, increasing the risk of injury or death.
Mitsubishi is recalling specific Lancer, Outlander, and Outlander Sport vehicles because front cross members may corrode and detach, increasing crash risk.
DTNA is recalling certain 2019-2021 Western Star 4700 and 5700 trucks. An undersized wire in the ground harness may cause a melted connector, leading to engine stall and increasing crash risk.
Mitsubishi is recalling 2019-2020 Outlander and 2019 Outlander PHEV vehicles because the right-side second-row seat belt may be assembled incorrectly, potentially failing to restrain occupants in a crash.