New Mexico recalls
3,431 federal recalls affecting New Mexico in the last 12 months - 99 New Mexico-specific plus 3,332 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA Flexible Cryoprobe devices
Erbe USA Inc. is recalling certain Flexible Cryoprobe surgical devices (model OD 1.7mm, L1.15mm, REF: 20402-410) because the probes may rupture or burst when activated during surgery. This defect could cause injury to patients or surgical staff. No injuries have been reported so far.
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA cryoprobes immediately
Erbe USA has recalled certain flexible cryoprobes used in surgery because they may rupture or burst when activated. The defect could cause unexpected device failure during a procedure. No injuries have been reported, but the risk requires immediate action.
- 2026-04-01FDA-FoodSiluetayaClass IStop using SiluetaYa Tejocote Roots supplement
SiluetaYa Mexican Tejocote Roots Supplement Pieces contain yellow oleander, a toxic plant that can cause serious illness. The affected product was sold online in Arizona, California, New Mexico, New York, Texas, and Utah. This is a Class I recall, the FDA's most serious category.
- 2026-04-01FDA-FoodNuts.comClass INationwideStop eating Nuts.com Espresso Malted Milk Balls
Nuts.com Espresso Malted Milk Balls contain wheat and soy allergens that are not listed on the package label. The ingredient soy lecithin contains soy, and wheat is also present in the product. People with wheat or soy allergies could have a serious reaction if they eat this product.
- 2026-04-01FDA-FoodAmerican LaboratoriesClass IIStop using American Laboratories Pepsin powder
American Laboratories is recalling Pepsin 1:3000 Powder (Item #FTI-G0193-00, Lot Code 00160041) because it may be contaminated with Salmonella. The affected powder was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported so far.
- 2026-04-01FDA-FoodAmerican LaboratoriesClass IIStop using American Laboratories pepsin powder
American Laboratories is recalling Pepsin 1:10,000 Powder (Item #FTI-G0193-00, Lot Code 00560021) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.
- 2026-04-01FDA-FoodAmerican LaboratoriesClass IIStop using American Laboratories Pepsin powder
American Laboratories is recalling Pepsin Full Strength Powder (Item #5000545, Lot Code 29460025) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.
- 2026-04-01FDA-FoodHerbal Creations USAClass IINationwideBulk packaged Colustrum Powder. packaged with generic product label.
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
- 2026-04-01FDA-FoodWestern MixersClass IINationwideStop using Treasured Harvest Chilli Spanish Peanuts
Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bag, lot #260230, expiration 1/23/2027) because glass fragments were found inside a sealed container. One case has been distributed to retail locations across the country.
- 2026-04-01FDA-FoodWestern MixersClass IINationwideStop eating First Street Chilli Spanish Peanuts
Western Mixers Produce & Nuts found glass inside sealed containers of First Street Chilli Spanish Peanuts (11oz). The affected products have lot numbers 260422, 260442, or 260543, with expiration dates between February 11–23, 2027. No injuries have been reported.
- 2026-04-01FDA-DrugAmerisourceClass IINationwideStop using recalled Meclizine Hydrochloride tablets
American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.
- 2026-04-01FDA-DrugTevaClass IINationwideStop using recalled Teva Octreotide Acetate injections
Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate 30 mg injectable suspension due to quality control problems found at the manufacturer. The FDA identified deficiencies that mean the sterility of these vials cannot be guaranteed. No injuries have been reported.
- 2026-04-01FDA-DrugTevaClass IINationwideStop using Teva Octreotide Acetate injections
Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension (20 mg) due to quality control issues at the manufacturing facility in Greece. The FDA found deficiencies that could affect sterility—the assurance that the medication is free from harmful bacteria and other microorganisms.
- 2026-04-01FDA-DrugTevaClass IINationwideStop using Teva Octreotide Acetate injection
Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.
- 2026-04-01FDA-DrugMacLeods PharmaClass IINationwideStop using Macleods Pharma levothyroxine tablets
Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.
- 2026-04-01FDA-DrugChiesiClass IINationwideStop using recalled CUROSURF lung surfactant
Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.
- 2026-04-01FDA-DrugRadnostixClass IIINationwideStop using Radnostix Gelatin Capsule Pack
Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.
- 2026-03-30FDA-PRBuy-herbal.comNationwideStop using Kian Pee Wan capsules immediately
Kian Pee Wan capsules, sold online as a dietary supplement for weight gain and appetite, contain two hidden prescription drugs: dexamethasone (a corticosteroid) and cyproheptadine (an antihistamine). These drugs were not listed on the label. Taking these undeclared drugs can cause serious health problems including infections, high blood sugar, psychiatric issues, and withdrawal symptoms if stopped abruptly.
- 2026-03-27FDA-PRSchreiber FoodsSchreiber Foods, Inc. Issues Allergy Alert on Undeclared Tree Nuts (Almonds) in Product
Schreiber Foods, Inc of Green Bay, WI is voluntarily recalling 144 Cases of Honey Almond Cream Cheese Spread, because it may contain undeclared almonds. People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this prod
- 2026-03-26CPSCBioenrrtyNationwideStop using MPINOI bed rails immediately
MPINOI brand adult portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 200 units were sold on Amazon between December 2025 and February 2026.
- 2026-03-26CPSCDIY Cold PlungeNationwideStop using DIY Cold Plunge Sauna Heater Kit
The electrical components in DIY Cold Plunge Sauna Heater Kits can overheat and create a fire hazard. The company has received 12 reports of units overheating, though no fires or injuries have occurred yet. The kits were sold online from March 2025 through February 2026.
- 2026-03-26CPSCSegmartNationwideStop using FUNTOK ride-on trucks immediately
FUNTOK 24V 2-Seater Ride-On Trucks (model DLS-K03) can overheat and catch fire due to a defective circuit board. The company has received 11 reports of fires, sparking, and smoking. No injuries have been reported yet, but the risk of serious burn injury is significant.
- 2026-03-26CPSCPetzlNationwideStop using Petzl ice climbing axes immediately
The aluminum shaft on Petzl Nomic and Ergonomic ice climbing axes can break at the handle during use, creating a fall hazard. This affects axes sold between December 2017 and March 2022. Petzl has received 26 reports of shaft breaks but no injuries so far.
- 2026-03-26CPSCMiddle Way ElectronicsNationwideStop using CCCEI power strips immediately
CCCEI-branded power strips sold online lack proper safety protection and can overheat and catch fire if too many devices are plugged in. Two units have already sparked and melted. The company is recalling about 5,500 units sold between April 2024 and January 2026.
- 2026-03-26CPSCGLMZZNationwideStop using GLMZZ magnet ball toys
GLMZZ Fidget Magnet Ball Toy Sets contain high-powered magnets that can be swallowed by children. If multiple magnets are ingested, they can attract each other inside the digestive system, causing perforations, blockages, or twisting of the intestines—which can lead to serious injury or death. The sets were sold on Amazon between February and October 2025.
- 2026-03-26CPSCSunnyyesNationwideStop using Sunnyyes LED mini lights immediately
Sunnyyes LED mini lights contain lithium coin batteries that children can easily access and swallow. The battery compartment screws can come loose, and the packaging lacks required safety warnings. Swallowing these batteries can cause serious internal burns and death.
- 2026-03-26CPSCDuraTracNationwideStop using DuraTrac gas connectors
DuraTrac stainless steel gas connectors sold between May and November 2025 contain a manufacturing defect that can cause gas leaks. These leaks pose a fire hazard. About 196,800 units are affected.
- 2026-03-26CPSCAirClubNationwideStop using AirClub convertible bassinets immediately
AirClub convertible bassinets (model QX-831) have a defective attachment mechanism that creates a dangerous gap between the bassinet and adult bed mattress. Infants can fall through this opening, causing serious injury or death. About 110,400 units were sold online between October 2023 and December 2025.
- 2026-03-26CPSCVive HealthNationwideStop using Vive Health bed rails immediately
Vive Health bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. Two deaths have been reported. The recall affects three models: Compact Bed Rail (LVA2009SLV), Bed Rail Collection V (LVA2097SLV), and Bed Rail model LVA1024 purchased on or before August 21, 2023.
- 2026-03-26CPSC4our KiddiesNationwideStop using 4our Kiddies furniture straps immediately
4our Kiddies plastic furniture straps (tip restraint kits) can break or degrade over time, allowing furniture to tip over and potentially trap or injure children or elderly people. The plastic brackets and cables fail to meet safety standards, and CPSC has received reports of at least 150 incidents where these straps broke, including three furniture tip-overs.
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