The Recall Desk

State

New Mexico product recalls

73,741 recalls have nationwide distribution and so reach New Mexico. 3,636 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total
3,636
Critical
745
Severe
815
Most recent
2026-10-28

Of the 3,636 recalls naming New Mexico we have scored against our rubric, 745 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 815 (22%) are Severe.

These figures cover only the 3,636 recalls whose distribution notice names New Mexico specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33876–33900 of 77377

  • LowFDA (Drugs)·D-1743-2019·2019-08-21

    Glenmark Recalls Clotrimazole and Betamethasone Cream Due to Temperature Abuse

    Glenmark Pharmaceuticals is recalling 31,224 tubes of Clotrimazole and Betamethasone Dipropionate Cream due to complaints of a liquidy texture caused by temperature abuse.

    Product
    CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE — CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE (CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·085-2019·2019-08-20

    Tip Top Poultry Recalls Fully Cooked Chicken Due to Listeria Risk

    Tip Top Poultry is recalling approximately 135,810 pounds of fully cooked diced chicken products due to possible Listeria monocytogenes contamination.

    Product
    Silver Comet Foods, LLC (FKA Tip Top Poultry Inc.) distributed by Tip Top — Tip Top Poultry, Inc. Recalls Fully Cooked Poultry Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V609000·2019-08-20

    Thor Motor Coach Recalls 2020 Motorhomes for Battery Cable Fire Risk

    Thor Motor Coach is recalling 1,941 2020 motorhomes because loose battery cables may cause electrical arcing and increase the risk of a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MAJESTIC, DAYBREAK, CHATEAU, OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E055000·2019-08-20

    Hale SmartFoam 6.5-12 Foam Pump Systems Recalled for Overheating Risk

    Hale Products Inc. is recalling SmartFoam 6.5-12 foam pump systems with 12-volt power supplies because they can overheat and fail, rendering fire-fighting foam unavailable.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V610000·2019-08-20

    Newmar Recalls 2018-2020 Motorhomes Due to Falling Bedroom Fascia Header

    Newmar is recalling 2018-2020 King Aire, Mountain Aire, and Essex motorhomes because the bedroom fascia header may fall onto the bed, increasing injury risk.

    Product
    NEWMAR — NEWMAR ESSEX, MOUNTAIN AIRE, KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19769·2019-08-19

    Club Car Recalls Gas Utility Vehicles Due to Fuel Leak Fire Risk

    Club Car is recalling approximately 1,300 gas utility and transport vehicles because a fuel vent may leak fuel, posing a fire hazard. No injuries have been reported.

    Product
    Club Car Gas Carryall 300, Transporter, Villager Vehicles, Streetrod Lux and Streetrod Vintage Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V608000·2019-08-19

    Horton Emergency Vehicles Recalled for Air Bag Cushion Defect

    Halcore Group is recalling 2018-2020 Horton Type I and III emergency vehicles because air bag cushions may detach and fail to inflate during a crash.

    Product
    HORTON — HORTON TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19770·2019-08-19

    Club Car Recalls Gas Golf Vehicles Due to Fire and Burn Hazards

    Club Car is recalling about 9,000 gas-powered golf and transport vehicles because a fuel line may leak, posing fire and burn hazards.

    Product
    Club Car Precedent, Tempo, Onward and Villager model gas golf and transport vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V606000·2019-08-16

    Kenworth T270 and T370 Recalled for Brake Hose Separation Risk

    PACCAR is recalling 2020 Kenworth T270 and T370 trucks because loose fittings may cause the brake air hose to separate, reducing braking ability.

    Product
    KENWORTH — KENWORTH T270, T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V604000·2019-08-16

    Forest River Recalls 2019 Rockport Vans Due to Welding Defect

    Forest River is recalling 2019 Rockport box vans and service bodies because improperly welded bulk storage beams may fail when loaded, posing an injury risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V605000·2019-08-16

    Mercedes-Benz Recalls 2019 CLS 450 for Electrical Wiring Defect

    Mercedes-Benz is recalling 2019 CLS 450 vehicles because an electrical line may chafe, causing engine stalls or electrical system failures that increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·084-2019·2019-08-15

    Tyson Recalls Weaver Chicken Patties Due to Foreign Matter Contamination

    Tyson Foods is recalling approximately 39,078 pounds of Weaver brand frozen chicken patties due to possible foreign matter contamination. Consumers should not consume these products.

    Product
    Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Weaver Brand Ready-To-Eat Chicken Patty Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E054000·2019-08-15

    Capco Recalls CTR Outer Tie Rods Due to Durability Concerns

    Capco USA is recalling CTR Outer Tie Rods because the taper on the ball studs may affect durability. This defect could impact vehicle control and increase crash risk.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V602000·2019-08-15

    Altec Recalls Aerial Devices Due to Winch Valve Defect

    Altec is recalling 2012-2019 aerial devices because a winch valve defect may allow lifting beyond rated capacity, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V603000·2019-08-15

    Land Rover Recalls 2018 Range Rovers for Backup Camera Software Defect

    Jaguar Land Rover is recalling 2018 Range Rover and Range Rover Sport vehicles because the backup camera may fail to display the rearview image, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1691-2019·2019-08-14

    RXQ Compounding Recalls Ondansetron Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Ondansetron 2 mg/mL Injection Solution because the product lacks assurance of sterility.

    Product
    ONDANSETRON 2 MG/ML INJECTION SOLUTION (PFV), 2 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0158-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1668-2019·2019-08-14

    RXQ Compounding Recalls Inositol/Choline B12:B6 Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Inositol/Choline B12:B6 injection solution because there is a lack of assurance of sterility.

    Product
    Inositol/Choline B12:B6, 50/50/1/0.175 MG/ML INJ SOLN(Sulfa Free Lipostat), 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0999-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2073-2019·2019-08-14

    St Jude Medical Recalls 21 Ellipse DR Implantable Cardioverter Defibrillators

    St Jude Medical is recalling 21 Ellipse DR implantable cardioverter defibrillators due to damaged aluminum wires that may prevent the delivery of high-voltage therapy.

    Product
    ELLIPSE DR, REF: CD2377-36QC Implantable cardioverter defibrillators (ICDs)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1666-2019·2019-08-14

    RXQ Compounding Recalls Hydroxocobalamin Injections Due to Sterility Concerns

    RXQ Compounding LLC is recalling Hydroxocobalamin 1000 mcg/mL injections because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.

    Product
    HYDROXOCOBALAMIN 1000 MCG/ML (PFV), 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0949-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1704-2019·2019-08-14

    RXQ Compounding Recalls Sodium Bicarbonate Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Sodium Bicarbonate 8.4% Injection due to a lack of assurance of sterility. The product is distributed nationwide.

    Product
    SODIUM BICARBONATE 8.4% (1 MEQ/ML) INJ SOLN (PFV), 50 ML PER VIAL, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0957-50
    Category
    Drug
    Distribution
    Distributed nationwide