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Recalls in New Mexico

Recalls sold in New Mexico, including nationwide recalls, newest first.
Agency
Risk level
Date
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9 recalls

B. Braun Spinal Needle Procedure Kits

Spinal Needle procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP, with potential quality issues.

High risk, FDA, Device defect

Entegra Qwest SE, Condor, Jayco Granite Ridge, and Melbourne Recreational Vehicles

The taillight warning light may incorrectly illuminate on the instrument panel display, potentially causing confusion and increasing crash risk.

NHTSA, Electrical system defect

2026 Entegra Qwest and Jayco Melbourne Prestige Recreational Vehicles

The taillight warning light may incorrectly illuminate on the instrument panel display, potentially causing confusion and increasing crash risk.

NHTSA, Electrical system defect

Aston Martin Valkyrie

The Aston Martin Valkyrie has a brake master cylinder seal that can deform, causing overheated brakes and a fire risk.

NHTSA, Brake defect

10 recalls

Spectra Medical Devices Lidocaine HCl Injection

Lidocaine HCl Injection USP may lack sterility.

Moderate risk, FDA, Sterility problem

Albertsons: 121 products

Albertsons foods contain undeclared allergens.

Moderate risk, FDA, Undeclared tree nut

Sato Yunker Energy & Health Herbal Supplement with Vitamins

This herbal supplement with vitamins does not meet label claim for Vitamin E.

Low risk, FDA, Wrong nutrient levels

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Tablets

Amlodipine and Olmesartan Medoxomil Tablets have failed dissolution specifications, with olmesartan medoxomil content below specifications.

Moderate risk, FDA, Drug dissolving problem

Shimadzu Digital Angiography and Radiography Systems

Digital Angiography Systems and a Digital Radiography System have electromagnetic contactors that may weld together.

Moderate risk, FDA, Device defect

Braun Ram ProMaster Seat Belts

Wheelchair seat belts may have incompatible connectors and fail to properly restrain occupants, increasing injury risk in a crash.

NHTSA, Seat belt defect

Kia Telluride and Kia Telluride Hybrid (2027)

The driver seat belt strap may not extend, failing to restrain an occupant in a crash and increasing injury risk.

NHTSA, Seat belt defect

Braun Chrysler Pacifica and Voyager Vehicles

Air bags may not deploy in certain Chrysler Pacifica and Voyager vehicles, increasing the risk of injury in a crash.

NHTSA, Air bag defect

Nova Bus LFS (1997-2002, 2005-2024) and Nova Bus LFS Artic (2009-2014, 2016-2024)

Nova Bus LFS transit buses have a low brake air pressure warning light that may fail to illuminate when the engine is off, increasing crash risk.

NHTSA, Brake defect

Daavlin Phothera 200 Phototherapy Devices

Phothera 200 Phototherapy Devices have calibration certificates with reversed outputs.

Moderate risk, FDA, Device defect

4 recalls

CASE v7.0 Cardiac Testing System

The CASE v7.0 Cardiac Testing System can spark at the printer head, potentially causing serious thermal injury.

Moderate risk, FDA, Device defect

Covidien EndoStitch Polysorb Single Use Loading Unit

The Covidien EndoStitch Polysorb Single Use Loading Unit may have holes in its pouch, compromising the sterile barrier.

Moderate risk, FDA, Sterility problem

Grand Design Reflection Fifth Wheel Recreational Trailers

Reflection fifth wheel trailers have shock bolts that may be incorrectly tightened, and broken parts can become a road hazard.

NHTSA, Suspension defect

Philips Azurion 3M12, 3M15, 5M12 and Other Angiography Systems

Philips Azurion systems may show a dark image during Roadmap Pro, not clinically usable.

Moderate risk, FDA, Device defect

6 recalls

Motor City Pizza Co. 5 Cheese Bread

Motor City Pizza Co. 5 Cheese Bread may be contaminated with Salmonella, which can cause serious infections.

Moderate risk, FDA, Salmonella

Eugia Lidocaine HCl Injection

Lidocaine HCl Injection has a label wrap that covers the barcode, making it hard to scan.

Low risk, FDA, Labeling error

Exacta Mix Vented Micro-Volume Inlet

Exacta Mix Vented Micro-Volume Inlet tubing sets may contain incorrect filters, causing reduced flow and clinical effects.

Moderate risk, FDA, Device defect

Becton Dickinson & Company BD Spinal Trays

BD Spinal Trays with Quincke or Whitacre needles have quality deficiencies related to acceptance testing.

High risk, FDA, Device defect

Forest River Salem (2024-2026), Forest River Stealth EVO (2026), and Forest River Wildwood (2024-2026)

The fireplace outlet may have incorrect wiring, increasing the amperage and risk of a fire.

NHTSA, Vehicle equipment defect

Mercedes-Benz GLE, GLS and Maybach Vehicles

The rear seat belt bolts may not be tightened properly, and a loose belt may not restrain an occupant during a crash.

NHTSA, Seat belt defect

17 recalls

MiniWarGaming and Primal Horizon Disc Magnets

Disc magnets violate the mandatory safety standard, posing a deadly ingestion hazard to children.

CPSC, Swallowing hazard

Panasonic-Branded Lithium Coin Batteries

The coin batteries are not in child-resistant packaging and lack required warning labels, which can cause serious injuries if swallowed.

CPSC, Swallowing hazard

Anzmtosn Luminous Fidget Spinner Balls

Luminous Fidget Spinner Balls have easily accessible button cell batteries that can cause serious injury or death if swallowed.

CPSC, Swallowing hazard

Misco Sports Light-Up Racket Sets

If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

CPSC, Swallowing hazard

Mainstays 9-Drawer Fabric Dressers

Mainstays 9-Drawer Fabric Dressers are unstable if not anchored, posing tip-over and entrapment hazards that can cause serious injury or death to children.

CPSC, Tip-over hazard

Medtronic 1x4 and 2x4 Pocket Adaptor Kit for Deep Brain Stimulation

The Medtronic Pocket Adaptor Kits are labeled with incorrect Use-By-Dates.

Moderate risk, FDA, Labeling error

Medline Anesthesia and Spinal Trays

Medline kits containing Huons Bupivacaine in Dextrose Injection have quality issues, including data integrity concerns and efficacy complaints.

High risk, FDA, Device defect

Philips Azurion and Allura Systems

The Azurion system may show decreased performance as it ages, potentially causing loss of imaging functionality.

Moderate risk, FDA, Device defect

Better Weather Actives Fix Elixir

Better Weather Fix Elixir may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl, which can cause nausea, vomiting, and other effects.

FDA

ARBOC Specialty Vehicles Spirit of Equess (2025) and 3 more

The wheelchair restraint retractor may not lock, allowing the wheelchair to move during transit.

NHTSA, Mobility equipment defect

IC Bus EVSB School Buses

The IC Bus EVSB school buses have improperly tightened mounting bracket bolts that can allow the drive motor to detach, posing a road hazard.

NHTSA, Electrical system defect

Forest River Bus Eldorado (2026), Forest River Van (2025-2026), and 7 more

Wheelchair restraint retractors may not lock, allowing the wheelchair to move during transit.

NHTSA, Mobility equipment defect

Subaru 2026 Forester and Forester Hybrid Vehicles

The moonroof glass panel may detach from the vehicle, becoming a road hazard.

NHTSA, Driver visibility defect

Mack Anthem, Pioneer, Pinnacle and Granite Trucks

The vehicles may have wheel lug nuts that loosen, allowing the wheel to detach and increasing crash risk.

High risk, NHTSA, Do not drive

Volvo VAH (2026), Volvo VHD (2026-2027), Volvo VN (2026-2027), and 2 more

Wheel lug nuts may loosen and allow the wheel to detach, causing loss of control or a road hazard.

High risk, NHTSA, Do not drive

2026 Chevrolet Express and GMC Savana Vehicles

The gear shifter may provide inaccurate gear selection feedback, which could lead to unexpected vehicle movement.

NHTSA, Steering defect

Abiomed Impella Controllers

The Automated Impella Controller has alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing.

High risk, FDA, Device defect

8 recalls

AbbVie Pred Mild Ophthalmic Suspension

Pred Mild ophthalmic suspension failed stability specifications.

Low risk, FDA, Quality testing problem

HydroMARK Breast Biopsy Site Marker

The HydroMARK Breast Biopsy Site Marker has incorrect inner package labeling.

Moderate risk, FDA, Labeling error

Tiffin Midas (2026), Tiffin Open Trail (2026-2027), and Tiffin Wayfarer (2026-2027)

The cargo carrying capacity label may be printed on a white label, which can make locating loading or tire pressure information difficult.

NHTSA, Vehicle equipment defect

Ember Touring Edition (2026-2027)

The shock bolts may be improperly tightened, causing broken parts to become a road hazard.

NHTSA, Suspension defect

Lexus GX (2024), Lexus UX Hybrid (2025), Toyota Land Cruiser Hybrid (2024-2025), and Toyota Mirai (2024)

The instrument panel display may fail to show warnings, increasing the risk of a crash or injury.

NHTSA, Electrical system defect

Ford Bronco Sport (2021-2026) and Ford Maverick (2022-2026)

The front lower control arm ball joints may detach, causing loss of vehicle control and crash risk.

High risk, NHTSA, Do not drive

Ford Expedition and Lincoln Navigator (2018-2022)

The seat belt may lock and fail to retract or extend, increasing injury risk in a crash.

NHTSA, Seat belt defect

Ford Bronco, Ford Explorer, and Ford Ranger (2025-2026)

The engine may fail, causing a sudden loss of drive power and increasing crash risk.

NHTSA, Engine defect

7 recalls

Omnipod 5 Pods, Omnipod DASH Pod, and Omnipod (Eros) Pod

Omnipod insulin pods may leak insulin due to cannula damage, causing under-delivery and high blood glucose.

High risk, FDA, Device defect