State
72,940 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,625 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 647 (18%) are Severe.
Which agencies issued them
These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Volkswagen is recalling certain 2025 Jetta and Taos vehicles because the instrument panel may fail to display warning lights or gauges. This fails FMVSS 101.
GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.
Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.
USDA FSIS issued a public health alert for raw Blackwing organic beef and pork products produced without federal inspection. Consumers are urged to discard or return these items.
Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.
Saputo Cheese USA is recalling Great Value Lowfat Cottage Cheese due to potential under-pasteurization caused by a broken pasteurizer seal. The product was distributed to ten states.
Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.
Clover Sonoma low-fat cottage cheese (16 oz and 32 oz sizes) is being recalled due to potential under-pasteurization from a broken pasteurizer seal. The product may not be safe for consumption.
Strides Pharma is recalling two lots of Children's Ibuprofen Oral Suspension after complaints of a gel-like mass and black particles in the product.
Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.
GE Medical Systems is recalling Centricity Universal Viewer software versions 7.0 through 7.0 SP2.0.1 because user login credentials may be exposed on the local client workstation.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423657, because the drainable large pouch may leak due to a manufacturing issue.
ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.
GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.
Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.
Volvo Trucks is recalling certain 2025–2026 VNL (4) vehicles because the instrument panel may fail while driving, potentially hiding critical safety information like the speedometer and warning lights.
Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.
Clover Sonoma sour cream (8 oz and 16 oz sizes) is being recalled because a broken seal on the pasteurizer may have resulted in underpasteurized product. The recall affects multiple states including California, Washington, and others.
LeMaitre Vascular is recalling one Artegraft Vascular Graft, REF AG740, because of a labeling mix-up resulting in the incorrect lot outer packaging of the product.
Stryker is recalling Cub Pediatric Cribs, model FL19H, because cribs sold in the USA are missing two access door warning labels.
Datascope is recalling the Battery Charging Station, model 0998-00-0802, because a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging.
Nova Bus is recalling certain 2016-2023 LFS and LFS Artic transit buses because the driver's seat belt tension-relieving device may fail to disengage without manual intervention. This fails FMVSS 208.
Toyota is recalling 2022-2024 Lexus LX vehicles because a seat frame issue may cause the front passenger air bag to deploy incorrectly during a crash.
Bentley is recalling 2025 Bentayga vehicles because the tire information placard may display incorrect tire size and pressure, increasing crash risk.