State

New Mexico product recalls

73,100 recalls have nationwide distribution and so reach New Mexico. 3,628 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,628
Critical: 747
Severe: 649
Most recent: 2026-09-23

Of the 3,628 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 649 (18%) are Severe.

Which agencies issued them

These figures cover only the 3,628 recalls whose distribution notice names New Mexico specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8451–8475 of 76728

HighFDA (Devices)·Z-0780-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline custom procedure kits containing non-sterile Codman Surgical Patties & Strips are being recalled due to potential endotoxin contamination. The recall affects 74 units distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2025·2025-01-08
Medtronic SynchroMed II and III Implantable Pumps Recalled for Software Defects
Medtronic is recalling SynchroMed II and III implantable pumps used with a clinician tablet app that has software issues in version 2.x. Approximately 319 systems were distributed worldwide.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0782-2025·2025-01-08
Medical Device Kits Recalled for Non-Sterile Surgical Components
Medline Industries is recalling See DocMan custom convenience kits that contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 48,655 units were distributed worldwide.
Product
See DocMan
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V003000·2025-01-08
Blue Bird Recalls 2024-2025 All American School Buses for Wiring Defect
Blue Bird is recalling 2024-2025 All American school buses because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2025·2025-01-08
Baxter SIGMA Spectrum Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter is recalling SIGMA Spectrum Infusion Pump (Version 6) units that were released after repair without complete flow testing. The incomplete testing poses a risk of improper device operation.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0174-2025·2025-01-08
Injectable phenylephrine recalled due to defective tamper-evident seals nationwide
Hikma Injectables is recalling phenylephrine injections nationwide because tamper-evident seals on some syringes were not properly attached. Affected lot 243120003D has a use-by date of 03/11/2025.
Product
phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0772-2025·2025-01-08
SynchroMed II and III implantable pumps recalled for software issues
Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk
Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0797-2025·2025-01-08
3M Unitek Orthodontic Primer Recalled Due to Bond Failures and Skin Irritation
3M Unitek is recalling Transbond Plus Self-Etching Primer used in orthodontic bonding due to reports of bracket bond failures and skin irritation or blistering.
Product
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self Etching Primer is an orthodontic all-in-one etchant and primer that is used in the bonding process of orthodontic appliances to teeth.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0783-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling 943 custom surgical kits containing non-sterile Codman Surgical Patties and Strips that may be contaminated with endotoxin.
Product
Medline custom medical procedure kits labeled as: 1) FREE FLAP BASIC SET-UP PK, REF DYNJ0991320J; 2) MVFF/FIBU #54-RF, REF DYNJ21927R; 3) FUNCTIONAL SINUS ENDOSCOPY, REF DYNJ40406A; 4) DR GOLDSTEIN ACCESSORY PACK, REF DYNJ51818F; 5) ENDOSCOPIC SKULL BASE, REF DYNJ58648
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0786-2025·2025-01-08
Medline Custom Surgical Kits Recalled for Non-Sterile Components with Endotoxin Risk
Medline Industries is recalling 3,903 custom medical procedure kits due to non-sterile Codman Surgical Patties and Strips with potential for endotoxin contamination. The recall affects products distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, REF DYNJ0660040R; 2) FREE FLAP PACK-LF, REF DYNJ42833A; 3) FREE FLAP PACK-LF, REF DYNJ42833B; 4) TYMPANOPLASTY PACK, REF DYNJ50692C; 5) MAJOR CRANIOTOMY SAFETY, REF DYNJ54736B; 6) FREE FLAP CU
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V004000·2025-01-08
Blue Bird Recalls 2025 All American Bus for Wiring Defect
Blue Bird is recalling one 2025 All American transit bus because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0792-2025·2025-01-08
Medline Medical Procedure Kits Recalled for Non-Sterile Component Contamination
Medline Industries is recalling 2,664 custom medical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The affected kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0175-2025·2025-01-08
Carboxymethylcellulose sodium eye drops recalled for label mix-up
AvKARE is recalling Carboxymethylcellulose Sodium Ophthalmic Solution eye drops due to a label mix-up. The recall affects 16,677 cartons distributed nationwide.
Product
CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0770-2025·2025-01-08
Auryon Laser Atherectomy System Recalled for Activation Failure
Angiodynamics is recalling 138 units of the Auryon atherectomy laser system due to potential failure to advance to activation mode during use. This malfunction could cause procedural delays or interruptions.
Product
AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0171-2025·2025-01-08
Dapsone Gel Recalled Nationwide for Crystallization
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% nationwide due to crystallization detected in multiple lots. Patients should contact their pharmacy or healthcare provider for guidance.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0168-2025·2025-01-08
AvKARE Nitrofurantoin 100 mg Capsules Recalled for Dissolution Failures
AvKARE is recalling Nitrofurantoin 100 mg capsules (NDC 50268-625-15, lot 47101, exp. 02/2026) nationwide because they failed dissolution specifications. Affected users should consult their healthcare provider.
Product
Nitrofurantoin Capsules, USP, 100 mg, 50 Capsules (5 x 10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478. NDC#: 50268-625-15.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0176-2025·2025-01-08
Eye drops recalled nationwide due to labeling mix-up
AvKARE is recalling Polyvinyl Alcohol Ophthalmic Solution eye drops due to a labeling mix-up. The recall affects Lot #0160 and was distributed nationwide.
Product
POLYVINYL ALCOHOL — POLYVINYL ALCOHOL (POLYVINYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0169-2025·2025-01-08
FDA Class III Atropine Sulfate Ophthalmic Solution Recall for Specification Failures
Somerset Therapeutics is recalling Atropine Sulfate Ophthalmic Solution due to failed impurity and degradation specifications. No illnesses have been reported.
Product
ATROPINE SULFATE — ATROPINE SULFATE (ATROPINE SULFATE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V002000·2025-01-06
Tesla Model X, Model Y, Model S, and Model 3 Rearview Camera Loss
Tesla is recalling certain 2023–2025 Model X, Model Y, Model S, and Model 3 vehicles because the computer circuit board may short, disabling the rearview camera image. This reduces rear visibility and increases crash risk.
Product
TESLA — TESLA MODEL 3, MODEL S, MODEL Y, MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25081·2025-01-02
Euqee Wintergreen Essential Oil Recalled for Unsafe Packaging
Euqee Wintergreen Essential Oils sold on Amazon.com are recalled because their packaging is not child-resistant, violating federal law. Methyl salicylate in the oil could poison young children if swallowed.
Product
Euqee Wintergreen Essential Oils
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V001000·2025-01-02
Aston Martin Vehicles Recalled: Infotainment Display Obstructs Rearview Camera
Aston Martin is recalling certain 2024-2025 DB12, Vantage, and DBX707 vehicles. The infotainment home screen menu may obstruct the rearview camera when in reverse, reducing rear visibility and increasing the risk of a crash.
Product
ASTON MARTIN — ASTON MARTIN DB12, DBX707, VANTAGE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25082·2025-01-02
Yaomiao Children's Jewelry Sets Recalled for Dangerous Lead and Cadmium Levels
Yaomiao children's jewelry sets sold on Amazon contain dangerous levels of lead and cadmium. Consumers should stop using them immediately, keep them away from children, and request a refund from the seller.
Product
Yaomiao Children's Jewelry Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25083·2025-01-02
John Deere ZTrak Zero-Turn Mowers Recalled for Fire and Burn Hazards
Kawasaki is recalling about 39,000 John Deere ZTrak zero-turn mowers with Kawasaki engines because the voltage regulator can fail, causing the engine to overheat and creating fire and burn hazards. No injuries have been reported to date.
Product
John Deere ZTrak™ Zero Turn Mowers with Kawasaki Engines
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0682-2025·2025-01-01
Blood Glucose Ketone Meter Firmware Bug Causes Inaccurate Test Results
Software bug in StatStrip Glucose Ketone Hospital Meter System can cause incorrect blood glucose and ketone test results to be transmitted to healthcare data systems. 347 units affected.
Product
StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683. Prescription use blood glucose ketone meter for near-patient testing
Category
Medical Device
Distribution
Distributed nationwide