State

New Mexico product recalls

73,509 recalls have nationwide distribution and so reach New Mexico. 3,629 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,629
Critical: 747
Severe: 813
Most recent: 2026-10-14

Of the 3,629 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 813 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,629 recalls whose distribution notice names New Mexico specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22676–22700 of 77138

HighFDA (Devices)·Z-0595-2022·2022-02-16
GE Healthcare MR Magnets Cryogenic Ventilation System Defect Recall
GE Healthcare is recalling 17,228 MR superconducting magnet systems because the cryogenic ventilation system may not meet required venting standards.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA PET/MR System, tomographic imager combining emission computed tomography with nuclear magnetic resonance system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0584-2022·2022-02-16
KWIK-STIK Quality Control Sets recalled for potential bacterial contamination
Microbiologics Inc is recalling KWIK-STIK QC Sets and Panels due to potential contamination with E. coli and Staphylococcus species. The affected product was distributed worldwide to laboratory testing facilities.
Product
QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Sets and Panels GP Comprehensive QC Set. Each KWIK-STIK unit contains a lyophilized microorganism pellet, an ampoule of hydrating fluid, and an inoculating swab. Each device is sealed within a laminated pouch that…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0562-2022·2022-02-16
Novalung Sensor Box Communication Failure May Disable Flow Measurement
The Novalung Sensor Box may experience communication failures between its flow sensor and sensor box component, potentially disabling flow measurement and air bubble detection. The recall affects 115 units distributed across 16 US states.
Product
Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)- Indicated for long-term (> 6 hours) respiratory/ cardiopulmonary support that provides assisted extracorporeal circulation and physiologic gas exchange (oxygenation and CO2 removal) of the patient's…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0635-2022·2022-02-16
Acufex Access Advanced Positioning Kit Recalled for Missing Sterilization
Smith & Nephew is recalling the Acufex Access Advanced Positioning Kit because the products were shipped to a distribution center instead of the sterilizer and were not sterilized before distribution.
Product
Acufex Access Advanced Positioning Kit - indicated for use to position and distract the extremity of patient during open and arthroscopic surgical procedures Product Number: 72205104
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0602-2022·2022-02-16
GE Healthcare MRI systems recalled for cryogen ventilation system defect
GE Healthcare Discovery MR450 MRI systems may have cryogen ventilation systems that do not meet required venting standards. The recall affects approximately 17,228 devices distributed in the U.S. and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR450 1.5T system, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0604-2022·2022-02-16
GE Healthcare MR Superconducting Magnets Recalled for Ventilation Defect
GE Healthcare recalled 17,228 superconducting magnets, a component of SIGNA 1.5T MR systems, due to a cryogen ventilation system that may not meet venting requirements. Systems are distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA 1.5T TwinSpeed MR System, nuclear magnetic resonance system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0596-2022·2022-02-16
GE Healthcare MRI Systems Recalled for Potential Cryogen Ventilation Defect
GE Healthcare is recalling approximately 17,228 SIGNA Creator and Explorer MRI systems due to potential defects in their cryogen ventilation systems that may not meet required venting standards.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Creator and SIGNA Explorer System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0594-2022·2022-02-16
GE Healthcare MRI Systems Recalled for Inadequate Cryogen Ventilation
GE Healthcare is recalling MRI superconducting magnets with cryogen ventilation system defects not meeting safety requirements. The recall affects 17,228 devices distributed across the US and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750 3.0T System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0605-2022·2022-02-16
GE Healthcare MR system magnets recalled due to cryogen ventilation defect
GE Healthcare is recalling 17,228 MR superconducting magnet components due to a cryogen ventilation system that may not meet required venting specifications.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Infinity MR System, SIGNA Infinity MR System with Excite Technology, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0586-2022·2022-02-16
Diagnostic Control Microorganism Recalled for Incorrect Test Results
Diagnostic control microorganisms manufactured by Microbiologics Inc are recalled for returning incorrect antibiotic susceptibility test results. These controls failed quality specifications and could cause inaccurate lab test results.
Product
LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic Control microorganisms
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0565-2022·2022-02-16
MIC Percutaneous Endoscopic Gastrostomy Kits Recalled for Oversized Retention Bolster
Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy (PEG) Kit because the external retention bolster may be oversized relative to the tube. Approximately 2,652 units have been distributed in the US, Canada, and Chile.
Product
MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0593-2022·2022-02-16
GE Healthcare MRI Systems Cryogen Ventilation System Defect Recall
GE Healthcare is recalling Discovery MR750w 3.0T MRI systems due to cryogen ventilation systems that may not meet FDA venting requirements. Approximately 17,228 devices were affected.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750w 3.0T System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0730-2022·2022-02-16
Amy's Vegan Rice Mac & Cheese Recall: Undeclared Milk Allergen
Amy's Kitchen is recalling its Vegan Organic Rice Mac & Cheese due to undeclared milk detected during testing. The product is labeled dairy-free, posing a risk to consumers with milk allergies.
Product
Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic overwrap, inside preprinted cardboard boxes; UPC 04227200432; Amy's Kitchen, Inc., P.O.Box 7129, Petaluma, CA 94955 8 or 12 retail units per case; Organic Gluten…
Category
Food
Distribution
33 states
HighFDA (Food)·F-0739-2022·2022-02-16
Lily's Peppermint Flavor Baking Chips Recalled for Undeclared Soy Allergen
Lily's Sweets is recalling 7 oz. pouches of Peppermint Flavor Baking Chips because they contain undeclared soy lecithin, a common allergen. The product was distributed to 22 U.S. states.
Product
Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch
Category
Food
Distribution
22 states
HighFDA (Devices)·Z-0634-2022·2022-02-16
Universal Chuck Surgical Instrument Handle May Detach and Release Ball Bearings
The Universal Chuck instrument handle may loosen and release ball bearings onto the surgical field. If not recovered, these bearings could delay surgery and potentially cause infection or tissue damage.
Product
Universal Chuck-The Universal Chuck is an Instrument Handle provided as an alternative instrument available for use in the TN-ADVANCED" Tibial Nailing System (TNA), TFN-ADVANCED" Proximal Femoral Nailing System (TFNA), RFN-ADVANCED" Retrograde Femoral Nailing System (RFNA)…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22083·2022-02-16
Valco Baby Snap Duo Trend Strollers recalled for front wheel breakage hazard
Valco Baby is recalling Snap Duo Trend strollers because the front wheels can break off during use, causing the stroller to fall unexpectedly. Consumers should stop using the stroller immediately and contact Valco Baby for a free replacement wheel assembly.
Product
Valco Baby Snap Duo Trend Strollers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0632-2022·2022-02-16
Orthopedic knee replacement component recalled for adhesive residue contamination
DePuy Orthopaedics is recalling 3 units of ATTUNE REVISION DISTAL FEMORAL AUGMENT due to adhesive residue that could cause tissue irritation or infection if not detected before surgery.
Product
ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0601-2022·2022-02-16
GE Healthcare MRI Cryogen Ventilation System Defect Recall
GE Healthcare is recalling 17,228 MRI systems due to a potential defect in the cryogen ventilation system that may not meet venting requirements. This Class II recall affects systems distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Optima MR450w 1.5T, Optima MR450w GEM system, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V567000·2022-02-16
2017-2021 Freightliner Cascadia Brake Lights May Remain Illuminated
Daimler Trucks North America is recalling 2017-2021 Freightliner Cascadia trucks because brake lights may remain illuminated after braking. This increases crash risk by making drivers unaware of actual braking.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0618-2022·2022-02-16
GE Healthcare MRI Systems Cryogenic Ventilation System Failure Recall
GE Healthcare is recalling 17,228 MR Vectra MRI systems because the cryogenic ventilation system may not meet required venting specifications.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare MR Vectra System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0609-2022·2022-02-16
GE Healthcare 1.5T SIGNA MRI systems recalled for ventilation defect
GE Healthcare is recalling 17,228 of its 1.5T SIGNA HDe MR imaging systems because the cryogenic ventilation system does not meet required venting standards.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare 1.5T SIGNA HDe MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0587-2022·2022-02-16
QC Control Materials KWIK-STIK AST-GP Produce Incorrect Test Results
Microbiologics Inc recalls KWIK-STIK AST-GP quality control materials that produce incorrect antibiotic susceptibility test results. Two lot numbers were distributed worldwide.
Product
QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V090000·2022-02-16
2022 Lucid Air suspension defect may cause brake failure and loss of control
Lucid Motors is recalling certain 2022 Lucid Air vehicles due to a failing snap ring in the front strut damper. This defect may result in sudden loss of ride height or brake line damage, increasing the risk of a crash.
Product
LUCID — LUCID AIR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0620-2022·2022-02-16
GE Healthcare Optima MR430s MRI systems have potential cryogenic ventilation defect
GE Healthcare recalled MR430s MRI systems because the cryogenic ventilation system may not meet required venting standards, creating potential safety risks.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Optima MR430s System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0600-2022·2022-02-16
GE Healthcare MRI Systems Recalled for Cryogen Ventilation Issue
GE Healthcare is recalling 17,228 SIGNA Artist MRI systems due to a potential defect in the cryogen ventilation system that may not meet safety venting requirements.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide