State

New Mexico product recalls

73,584 recalls have nationwide distribution and so reach New Mexico. 3,630 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,630
Critical: 747
Severe: 813
Most recent: 2026-10-21

Of the 3,630 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 3,630 recalls whose distribution notice names New Mexico specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24576–24600 of 77214

HighFDA (Devices)·Z-2384-2021·2021-09-08
MY01 Continuous Compartmental Pressure Monitor Recalled for Out-of-Specification Needle
MY01, INC. is recalling the MY01 Continuous Compartmental Pressure Monitor (37 units) due to an incorrect needle with out-of-specification trocar geometry. The affected devices may require higher force to penetrate patient skin.
Product
MY01 Continuous Compartmental Pressure Monitor, Reference Number MY01-0001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2382-2021·2021-09-08
FDA Recalls COVID-19 Antibody Test Kits for Increased False Positive Risk
Thera Test Laboratories is recalling EL-Anti-SARS-CoV-2 IgG kits due to cross-reactivity that may produce false positive results. The recalled lot numbers are 05204351 and 05204368, affecting distribution in six US states.
Product
EL-Anti-SARS-CoV-2 IgG Kit, Catalog #104-130. Submitted as EUA202128
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2383-2021·2021-09-08
CoolSculpting Elite System Software Error May Misreport Thermal Events
The CoolSculpting Elite System may incorrectly report or fail to report thermal events during treatment, potentially causing unnecessary re-treatment or continued use without awareness of a malfunction.
Product
CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2380-2021·2021-09-08
Surgical Instrument Recall: Failed Adhesive May Cause Tissue Burns
Olympus recalls Gyrus Acmi PKS surgical instruments due to expired adhesive that could fail, potentially causing foreign body reactions or electrical burns to patients.
Product
Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation, mechanical grasping, and dissection of tissue during the performance of laparoscopic and general open surgical procedures when used in conjunction with the Gyrus ACMI G400 workstation Ref: 970010PC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2404-2021·2021-09-08
Siemens Artis Angiography Systems Software Error May Delay Clinical Treatment
Certain Siemens Artis angiography systems with software version VD12 may fail to start up properly due to a software error, potentially delaying clinical imaging procedures. The issue affects specific units identified by serial number.
Product
Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP 10094139 Artis Q floor 10848280 Artis Q ceiling 10848281 Artis Q biplane 10848282 Artis Q.zen floor 10848353 Artis Q.zen ceiling 10848354…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2409-2021·2021-09-08
Healgen COVID-19 Rapid Test Cassette Recalled Due to Unauthorized Laboratory Distribution
Healgen COVID-19 IgG/IgM Rapid Test Cassettes were distributed to laboratories not certified under CLIA, violating Emergency Use Authorization requirements. Unauthorized labs may produce inaccurate test results.
Product
Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) Qualitative detection and differentiation of IgM and IgG antibodies against SARS-CoV-2 in human venous whole blood, plasma (Li+- heparin, K2-EDTA and sodium-citrate), and serum. Intended for use as an aid…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2388-2021·2021-09-08
Surgical arm suspension kits recalled due to sterilization concerns
Aspen Surgical Products is recalling Jessie Sterile Arm Suspension Kits due to bioburden levels exceeding sterilization validation limits. This may compromise the sterile field and increase infection risk.
Product
Jessie Sterile Arm Suspension Kit, Product Code 711300, (previous product code 100401), Sample Kit S711300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0789-2021·2021-09-08
China-Gel Topical Pain Reliever Recalled for Manufacturing Facility Contamination
China-Gel Inc is recalling China-Gel White topical pain reliever products due to potential contamination with Burkholderia cepacia found at the manufacturing facility. The recall affects multiple package sizes distributed nationwide and internationally.
Product
CHINA-GEL — CHINA-GEL (MENTHOL AND CAMOHOR (SYNTHETIC))
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0788-2021·2021-09-08
China-Gel Topical Pain Reliever Recall Due to Manufacturing Contamination
China Gel Inc is recalling China-Gel (menthol and camphor) topical pain reliever products due to contamination with B. cepacia found in the manufacturing facility where the product was made.
Product
CHINA-GEL — CHINA-GEL (MENTHOL AND CAMOHOR (SYNTHETIC))
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0790-2021·2021-09-08
Topical Pain Relief AULIEF Recalled for Facility Contamination Risk
China Gel Inc is recalling AULIEF topical pain relief (menthol and camphor) because the product was manufactured in a facility where Burkholderia cepacia contamination was found in other products.
Product
AULIEF — AULIEF (MENTHOL AND CAMOHOR)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0957-2021·2021-09-08
Hostess Soft White Hamburger Buns Recalled for Listeria and Salmonella Risk
Hostess Brands, LLC is recalling Hostess Soft White Hamburger Buns because the contract manufacturer detected positive environmental samples for Listeria and Salmonella species. The affected product was distributed to retailers and distributors across 34 states.
Product
Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987
Category
Food
Distribution
35 states
HighFDA (Drugs)·D-0786-2021·2021-09-08
Akorn Artificial Tears Ointment Recalled for Non-Sterility
Akorn, Inc. is recalling Artificial Tears Ointment eye lubricant due to failure of sterility testing. The product may be contaminated with Bacillus cereus.
Product
Artificial Tears Ointment, Lubricant Eye Ointment, Net Wt. 3.5 g (1/8 oz.) per tube, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-062-35
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2386-2021·2021-09-08
Peripheral Atherectomy Devices Recalled Due to Crown Size Mislabeling
Cardiovascular Systems Inc is recalling STEALTH 360 GEN2 peripheral atherectomy devices due to potential mislabeling of crown sizes. Some 1.50mm crowns may be labeled as 1.25mm and vice versa, potentially affecting device performance.
Product
STEALTH 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.25MM MICRO, 145 CM, REF PRD-SC30-MICRO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2390-2021·2021-09-08
Norton Arm Kit surgical device recall due to sterilization failure
Aspen Surgical Products is recalling 124 Norton Arm Kits due to bioburden levels exceeding sterilization validation limits, creating potential risk of surgical site infection.
Product
Norton Arm Kit, Product Code 711400, (previous product code 031001), Sample Kit S711400
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2408-2021·2021-09-08
FaStep COVID-19 Test Devices Recalled for Unauthorized Laboratory Distribution
Versea Diagnostics recalled 563,290 FaStep COVID-19 antibody test devices that were distributed to laboratories not certified under federal standards. The devices were authorized only for use in CLIA-certified laboratories.
Product
FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium EDTA), serum, plasma (sodium EDTA) and fingerstick whole blood. Intended for use as an aid in identifying individuals…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0775-2021·2021-09-08
Cyclobenzaprine Hydrochloride Tablets 7.5mg Recalled for Microbial Contamination
Teva Pharmaceuticals USA is recalling Cyclobenzaprine Hydrochloride Tablets 7.5mg due to out-of-specification microbial test results in an excipient batch. The affected product was distributed nationwide.
Product
Cyclobenzaprine Hydrochloride Tablets, 7.5mg, 100 count tablets per bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314, NDC 70199-014-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0774-2021·2021-09-08
Cyclobenzaprine Hydrochloride Tablets 7.5mg Recalled for Microbial Contamination
Teva Pharmaceuticals is recalling Cyclobenzaprine Hydrochloride Tablets 7.5mg due to out-of-specification microbial counts in an ingredient batch. The product was distributed nationwide.
Product
Cyclobenzaprine Hydrochloride Tablets, 7.5mg, 100 count tablets per bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 0591-3330-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0787-2021·2021-09-08
Clopidogrel Tablets Recalled for Foreign Matter Contamination
Macleods Pharma USA is recalling Clopidogrel 75 mg tablets due to the presence of foreign matter in the product. The affected lot was distributed nationwide.
Product
CLOPIDOGREL — CLOPIDOGREL (CLOPIDOGREL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2393-2021·2021-09-08
Steripath Luer Transport Pack Gen2 Recalled for Incorrect Instructions
Magnolia Medical Technologies is recalling 9,400 units of Steripath Luer Transport Pack Gen2 because they were shipped with incorrect Transfer Adapter Instructions For Use (IFU).
Product
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2407-2021·2021-09-08
COVID-19 diagnostic test distributed outside certified laboratory channels
CareStart COVID-19 Antigen Rapid Diagnostic Test units were distributed to non-CLIA-certified customers, violating the product's Emergency Use Authorization requirements.
Product
CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals suspected of COVID-19 by…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0785-2021·2021-09-08
Lidocaine Ointment USP 5% Recalled for Failed Viscosity Specifications
Teligent Pharma is recalling Lidocaine Ointment USP 5% (114,456 tubes, Lots 15378 and 14418) distributed nationwide because certain lots do not meet viscosity specifications, as determined through routine testing.
Product
Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-008-14.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0784-2021·2021-09-08
Donepezil HCL Tablets 5 mg Recalled for Subpotency
Jubilant Cadista Pharmaceuticals is recalling Donepezil HCL Tablets, USP, 5 mg (Lot # DN120006A, exp. 12/2021) because the tablets are subpotent—meaning they contain less active ingredient than specified. The recall affects 14,544 bottles distributed nationwide.
Product
Donepezil HCL Tablets, USP, 5 mg, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd. India, Marketed by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 NDC 59746-329-90
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V694000·2021-09-07
Eldorado EZRM Recalled for Fuel Hose Leak Fire Risk
Eldorado National is recalling 2019-2021 EZRM vehicles with L9 Diesel Engines due to a fuel hose leak that increases fire risk.
Product
ELDORADO — ELDORADO EZRM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V693000·2021-09-07
LDJ Recalls 2021 Thunder Creek Trailers Due to Fender Light Wiring Defect
LDJ Manufacturing is recalling 279 2021 Thunder Creek trailers because improperly routed wiring may cause fender clearance lights to fail, increasing crash risk.
Product
THUNDER CREEK — THUNDER CREEK STT, MTO, SLT, MTT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E084000·2021-09-04
Nineo F2-H11 LED Bulbs Recalled for Excessive Brightness
Nineo is recalling F2-H11 replacement LED bulbs because they may be too bright, posing a glare hazard to oncoming drivers.
Product
EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
Category
Vehicle
Distribution
Distributed nationwide