State

New Mexico product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23201–23225 of 77196

ModerateFDA (Drugs)·D-0335-2022·2022-01-12
CVS Allergy Relief Fexofenadine Tablets Recalled for Impurity
CVS Allergy Relief Fexofenadine Hydrochloride Tablets 60 mg are being recalled because stability testing found an out-of-specification result for impurity A. The recall affects approximately 138,144 containers distributed nationwide.
Product
CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 60 mg Antihistamine, 12HR, packaged as a) 12 count bottle, NDC 59779-425-53, UPC 0 50428 25414 1; b)24 count bottle, NDC 59779-425-62, UPC 0 50428 53435 9; Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI…
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V009000·2022-01-11
Oshkosh Recalls 2019-2022 S-Series Vehicles Due to Front Axle Bolt Failure Risk
Oshkosh is recalling 2019-2022 S-Series vehicles because front axle u-bolts may fail, potentially allowing the axle to shift or detach and increasing crash risk.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·22045·2022-01-11
Bella Residential Elevators Recalled for Child Entrapment Hazard
Bella residential elevators pose a risk of child entrapment between exterior and interior doors. Young children can become trapped and suffer serious injuries or death when the elevator moves to another floor.
Product
Bella residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·22047·2022-01-11
Residential Elevators Recalled for Child Entrapment Hazard
Savaria and Garaventa residential elevators pose an entrapment risk to young children due to gaps between doors. Young children can become trapped and suffer serious injury or death when the elevator is called to another floor.
Product
Savaria and Garaventa branded residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V007000·2022-01-11
Play-Mor Trailers Recalled Due to Propane Regulator Fire Risk
Play-Mor is recalling specific 2017-2020 trailers because a propane regulator may fail, increasing pressure and fire risk. Dealers will replace the parts free of charge.
Product
PLAY-MOR — PLAY-MOR MOTORSPORT SUV TRAILER, SINGLE ROOM TRAILER, 2 ROOM TRAILER, BBQ TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22046·2022-01-11
Inclinator residential elevators recalled for child entrapment hazard
Inclinator Company of America is recalling residential elevators manufactured from 1979 through 2021 because young children can become entrapped between the exterior landing door and interior elevator car door, risking serious injury or death.
Product
Inclinator residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V008000·2022-01-11
Oshkosh Recalls 2019-2022 S-Series Vehicles Due to Fuel Leak Fire Risk
Oshkosh is recalling 2019-2022 S-Series vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V006000·2022-01-10
Reading Truck Recalls Marauder Dump Bodies Due to Weld Failure Risk
Reading Truck Body is recalling 2017-2021 Marauder Landscape Dump Body vehicles because a rear pivot mount weld may fail, increasing injury risk.
Product
READING TRUCK — READING TRUCK MARAUDER DUMP
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·003-2022·2022-01-08
Abbyland Foods Recalls Beef Sticks for Undeclared Milk Allergen
Abbyland Foods is recalling approximately 14,976 pounds of smoked beef sticks because they contain undeclared milk, a known allergen.
Product
Abbyland Foods, Inc. Recalls Beef Stick Product Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22V005000·2022-01-07
Lakota Recalls 2021-2022 Trailers Due to Tire Belt Separation Risk
Lakota is recalling 2021-2022 Bighorn, Charger, and Livestock trailers because certain tires may experience belt separation, increasing crash risk.
Product
LAKOTA — LAKOTA CHARGER, BIGHORN, LIVESTOCK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V003000·2022-01-07
2022 Forest River Aurora travel trailers recalled for furnace cooktop fire risk
Forest River is recalling 2021-2022 Aurora and Catalina travel trailers because the panel sealing the cooktop from the furnace was not properly sealed, which could cause an inverted flame and fire risk.
Product
COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V004000·2022-01-07
2022 Forest River Cardinal Trailers Recalled for Tire Belt Separation
Forest River, Inc. is recalling certain 2021-2022 fifth wheel trailers equipped with defective Sailun tires that may experience belt separation. The defect could cause loss of vehicle control and increase the risk of a crash.
Product
PRIME TIME — PRIME TIME, FOREST RIVER, CONTINENTAL CARGO SANIBEL, CARDINAL, CRUSADER, CONTINENTAL CARGO
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·001-2022·2022-01-06
Interstate Meat Dist. Recalls Ground Beef Due To E. Coli O157:H7
Interstate Meat Dist. Inc. is recalling approximately 28,356 pounds of ground beef products due to possible E. coli O157:H7 contamination.
Product
Interstate Meat Dist. Inc., Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
Distributed nationwide
HighCPSC·22716·2022-01-06
Polaris Outlaw 110 EFI Youth ATVs Recalled for Fire Hazard
Polaris is recalling about 1,100 Model Year 2022 Outlaw 110 EFI Youth ATVs because the inner layer of the fuel line can leak, posing a fire hazard. No fires or injuries have been reported.
Product
Outlaw 110 EFI Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·002-2022·2022-01-06
Kettle River Recalls Chicken Alfredo Pizza for Undeclared Wheat Allergen
Kettle River Products is recalling approximately 1,464 pounds of chicken alfredo pizza due to misbranding and an undeclared wheat allergen. No adverse reactions have been reported.
Product
Kettle River Products Recalls Chicken Alfredo Pizza Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighCPSC·22715·2022-01-06
Children's Covered Wood Wagons Recalled for Excessive Lead Paint
Colony Brands is recalling about 20 covered wood wagons sold through Montgomery Ward's and Ginny's from September to October 2021 because paint on the wood, plastic handles, and red plastic cover contains excessive lead that can be toxic if ingested by young children.
Product
Covered Wood Wagons
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0363-2022·2022-01-05
kleantouch Hand Sanitizer recalled for methanol contamination
Valisa MFG LLC is recalling kleantouch Hand Sanitizer 8 FL OZ pump bottles nationwide because the product contains methanol and was marketed without FDA approval. Consumers should stop using the product immediately.
Product
kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC, Farmingdale, NY, 11735, Made in USA, UPC 6 86162 99246 1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0323-2022·2022-01-05
SterRx Phenylephrine HCl Injection Recalled for Sterility Assurance
SterRx is recalling PHENYLephrine HCl 40 mg per 250 mL injectable solution nationwide due to lack of assurance of sterility. The recall affects approximately 20,640 bags distributed across the United States.
Product
PHENYLephrine HCl, 40 mg per 250 mL, (160 mcg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-252-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0315-2022·2022-01-05
dilTIAZem HCl in Dextrose Injection Recalled for Sterility Assurance
SterRx is recalling dilTIAZem HCl in 5% Dextrose Injection due to lack of assurance of sterility. The recall affects 8,946 bags distributed nationwide.
Product
dilTIAZem HCl in 5% Dextrose Injection, 125 mg per 125 mL, (32 mcg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-951-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0319-2022·2022-01-05
SterRx Norepinephrine Injection Recalled for Lack of Sterility Assurance
SterRx is recalling 1,044 bags of Norepinephrine 16 mg per 250 mL in 5% Dextrose Injection nationwide due to lack of assurance of sterility. The affected product carries NDC 70324-002-01 with lot code S21194/CDW.
Product
NOREPINEPHRINE, 16 mg per 250 mL, (64 mcg per mL) in 5% Dextrose Injection, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-002-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0354-2022·2022-01-05
BUBS Naturals Collagen Supplement Recalled for Undeclared Milk
BUBS Naturals Fountain of Youth Formula collagen supplement is recalled nationwide because it contains undeclared milk from an MCT oil powder ingredient. Consumers with milk allergies or sensitivities should not consume this product.
Product
BUBS Naturals Fountain of Youth Formula; Collagen Protein; Support for Hair, Skin & Nails; Biotin, Antioxidant, Vitamin C; Maqui Berry Net Wt. 10.16 oz. (288 g)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0317-2022·2022-01-05
SterRx Fentanyl Citrate Injection recalled for lack of sterility assurance
SterRx is recalling Fentanyl Citrate in 0.9% Sodium Chloride Injection (2.5 mg per 250 mL) distributed nationwide due to lack of assurance of sterility.
Product
Fentanyl Citrate, in 0.9% Sodium Chloride Injection, 2.5 mg per 250 mL, (10 mcg per mL), Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-327-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0313-2022·2022-01-05
Morphine Sulfate Injection Recalled for Lack of Sterility Assurance
SterRx is recalling 40 bags of Morphine Sulfate in 5% Dextrose Injection (1 mg per mL) distributed nationwide due to lack of assurance of sterility. The product is subject to contamination risk.
Product
Morphine Sulfate in 5% Dextrose Injection, 100 mg per 100 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-452-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0300-2022·2022-01-05
SterRx Midazolam Injection Recalled for Lack of Sterility Assurance
SterRx, LLC is recalling Midazolam in 0.9% Sodium Chloride Injection (50 mg per 50 mL) distributed nationwide due to lack of assurance of sterility. The recall affects 15,660 bags from seven lots manufactured between November and December 2021.
Product
Midazolam in 0.9% Sodium Chloride Injection, 50 mg per 50 mL (1 mg per mL), Rx only, SterRx, 141 Idaho Ave. Plattsburgh, NY 12003, NDC #70324-102-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0305-2022·2022-01-05
Phenylephrine HCL Injection Recalled for Lack of Sterility Assurance
SterRx is recalling approximately 18,948 bags of Phenylephrine HCL in 0.9% Sodium Chloride injection nationwide due to lack of assurance of sterility. The product is distributed across the U.S.A.
Product
PHENYLepherine HCL in 0.9% Sodium Chloride, 20 mg per 250 mL (80 mcg per mL), Rx only, SterRx, 141 Idaho Avenue, Plattsburgh, NY 12903, NDC 70324-701-01.
Category
Drug
Distribution
Distributed nationwide