New Mexico recalls
3,444 federal recalls affecting New Mexico in the last 12 months - 82 New Mexico-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using recalled DayQuil liquid
DayQuil liquid (12/8oz bottles) distributed by Gold Star Distribution Inc. was stored in conditions that did not meet safety standards, including exposure to rodents at their distribution center. All unexpired lots distributed by this company are affected. No injuries have been reported.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using recalled DayQuil Cold & Flu
DayQuil Cold & Flu 32-count twin packs distributed by Gold Star Distribution may have been stored in insanitary conditions with rodent activity at a distribution center. The FDA is recalling all lots still within their expiration date that were distributed nationwide.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using Claritin from Gold Star Distribution
Gold Star Distribution Inc. distributed Claritin 20-count tablets that were stored in conditions with rodent exposure and activity at their distribution center. The FDA found insanitary conditions that violate manufacturing standards. This affects all lots of this product distributed by Gold Star that are still within their expiration date.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using Bayer 2Pk 25 CT products
Bayer products distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and other sanitation issues at their distribution center. The FDA is recalling all lots that are still within their expiration date.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideCheck your Benadryl 25-count 2-pack for recall
Gold Star Distribution Inc. distributed Benadryl 25-count 2-packs (UPC 815556020316) from a distribution center with insanitary conditions and evidence of rodent activity. The contamination risk affects all lots that were within expiration and distributed by this company across the United States.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using recalled Alka-Seltzer products
Alka-Seltzer Original (58-count boxes) and Plus Cold & Flu (36-count boxes) distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and activity. The FDA found unsanitary conditions at the distribution center that do not meet manufacturing safety standards.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using Aleve 1's from Gold Star Distribution
Gold Star Distribution Inc. distributed Aleve 1's (60-count bottles) that were stored in conditions that did not meet safety standards. The distribution center had insanitary conditions and evidence of rodent activity. All unexpired lots distributed by this company are affected.
- 2026-01-21FDA-DrugGold Star DistributionClass IINationwideStop using recalled Advil products
Advil Ibuprofen and Advil PM dispenser packs distributed by Gold Star Distribution Inc. were stored in conditions that did not meet safety standards, including rodent exposure at their distribution center. The affected products were distributed nationwide. No injuries have been reported.
- 2026-01-21FDA-DrugEncon Safety ProductsClass IINationwideCheck your Aquarion Preserved Cartridges lot number
Encon Safety Products is recalling specific lots of AQ 120 GFEW Aquarion Preserved Cartridges due to manufacturing process deviations that do not meet FDA standards. The cartridges were distributed nationwide. No injuries have been reported.
- 2026-01-21FDA-DrugAlvogenClass IINationwideCheck your Alvogen Thyro-Tabs levothyroxine bottle
One bottle of Alvogen Thyro-Tabs 150mcg levothyroxine tablets (Lot MHA21825) was found to contain 88mcg tablets instead of the labeled 150mcg strength. This mix-up affects only a single bottle distributed nationwide. No injuries have been reported.
- 2026-01-21FDA-DrugSun PharmaceuticalClass IIINationwideStop using Sun Pharmaceutical clindamycin solution
Sun Pharmaceutical has recalled three lots of clindamycin phosphate 1% topical solution due to failed quality tests. The affected batches contain higher-than-acceptable impurities and may not contain the correct amount of active ingredient, which could reduce effectiveness.
- 2026-01-21FDA-DrugSun PharmaceuticalClass IIINationwideStop using recalled fluocinolone acetonide solution
Taro Pharmaceuticals is recalling specific lots of fluocinolone acetonide topical solution (0.01%) because testing found higher-than-allowed levels of an impurity. The affected lots were distributed nationwide. No injuries have been reported.
- 2026-01-15CPSCShangYu North Electron ManufactureNationwideStop using recalled Frigidaire minifridges immediately
Frigidaire-brand minifridges sold at Target can overheat and catch fire due to faulty electrical components. Curtis International has received six reports of fires in the EFMIS121 model, with property damage. The recall now includes about 330,000 additional units across five model numbers.
- 2026-01-15CPSCRonghuiNationwideStop using RootStim Beard Growth Serum
RootStim Beard Growth Serum spray bottles contain minoxidil, a powerful medication that must be in child-resistant packaging by law. These bottles do not have child-resistant caps, creating a serious risk of poisoning if a young child swallows the liquid. The product was sold online from November 2024 through September 2025.
- 2026-01-15CPSCGreataleNationwideStop using Greatale self-feeding pillows
Greatale self-feeding pillows can hold a bottle at an unsafe angle that an infant cannot pull away from, risking aspiration of milk or formula and suffocation. About 1,260 pillows were sold online through Amazon between September 2024 and July 2025.
- 2026-01-15CPSCKebenNationwideStop using HEZI power strips immediately
HEZI brand power strips with gray or yellow metal enclosures can cause serious electric shock or death if the metal case becomes energized. The strips lack proper grounding and were sold online from May 2024 through October 2025. No injuries have been reported yet, but the risk is serious.
- 2026-01-15CPSCMorgan LaneNationwideStop using Morgan Lane Asher Pajamas immediately
Morgan Lane Asher Pajama Sets (Style 816TR in Petal, sizes 2T–14) fail to meet federal flammability standards for children's sleepwear and pose a serious burn hazard. These cotton pajamas with tiny rose prints were sold online from March 2024 through May 2025.
- 2026-01-15CPSCAdams ManufacturingNationwideStop using Adams Adirondack patio chairs
Adams Manufacturing recalled Adirondack-style resin patio chairs sold at Lowe's and Home Depot because they can crack and collapse during use, creating a fall and injury risk. About 6,100 chairs are affected, sold from August through October 2025 in multiple colors.
- 2026-01-15CPSCYixing TradingNationwideStop using KEAWIS crib mattresses immediately
KEAWIS crib mattresses (model XX-BM-01) may not fit properly in certain play yards or smaller cribs, creating dangerous gaps where babies can become trapped or suffocate. The mattresses do not meet federal safety standards for crib mattresses. About 1,500 units were sold online through Amazon between August 2024 and July 2025.
- 2026-01-15CPSCR.X.YNationwideStop using R.X.Y bicycle helmets immediately
R.X.Y-branded adult bicycle helmets sold on Amazon do not meet federal safety standards for impact protection and stability. In a crash, these helmets may fail to protect your head, creating a serious risk of injury or death.
- 2026-01-15CPSCLSY DirectNationwideStop using BBWOO baby loungers immediately
BBWOO baby loungers have sides that are too low to safely contain an infant and openings that are wider than safety standards allow, creating fall and entrapment hazards. The loungers also lack a stand, which can cause them to fall if placed on elevated surfaces. These design flaws violate mandatory infant sleep product safety standards.
- 2026-01-15CPSCEnergizerNationwideStop using Energizer rechargeable lanterns immediately
Energizer is recalling about 4,100 Large Power Indicator Lanterns (model BGAAL9) with June 2024 date codes because the lithium-ion batteries can overheat and cause burns. One overheating incident has been reported, though no injuries so far.
- 2026-01-15CPSCRuahouineNationwideSecure Ruahouine Hair Growth Serum away from children
Ruahouine Hair Growth Serum bottles contain minoxidil, a powerful chemical that can cause serious poisoning if swallowed. The bottles do not have child-resistant caps as required by law, making it easy for young children to open and ingest the contents. About 25,000 bottles were sold on Amazon between January and July 2025.
- 2026-01-14FDA-DeviceIntegra LifeSciencesClass IINationwideCheck Codman CereLink ICP Sensor lot numbers
The 14-gauge Tuohy needle included in certain Codman CereLink ICP Sensor Basic Kits may have corrosion stains on its surface. These kits are used by hospitals and surgical centers for monitoring intracranial pressure during brain procedures. Integra LifeSciences is recalling specific lot numbers distributed worldwide.
- 2026-01-14FDA-DeviceIntegra LifeSciencesClass IINationwideCodman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only.
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
- 2026-01-14FDA-DeviceMedlineClass IINationwideStop using Medline Hudson RCI oxygen masks
Medline Industries is recalling multiple models of Hudson RCI oxygen masks because the tubing can disconnect during use. If this happens, oxygen delivery stops, which can delay patient care and cause breathing problems that may require medical intervention.
- 2026-01-14FDA-DeviceIMRISClass IINationwideStop using affected IMRIS HFD100 devices
The torque screw in certain IMRIS HFD100 Head Fixation Devices may crack or separate during use. This could cause the device to fail to hold a patient's head securely during surgery, potentially affecting surgical accuracy and requiring emergency use of backup fixation methods.
- 2026-01-14FDA-DevicePhilipsClass IINationwideCheck your Philips MX40 patient monitor
Philips MX40 patient monitors may lose wireless connection to the PIC iX central station when moving between certain access points if the signal strength changes rapidly. This could interrupt patient data transmission to clinical staff.
- 2026-01-14FDA-DeviceSecuritas HealthcareClass IINationwideCheck your Securitas Healthcare call station
Securitas Healthcare identified a firmware problem in certain Arial 900 MHz Call Station units (Model CSK200-900MR, Firmware 1.6.3) sold between January 2023 and June 2024. The affected units may fail to send a low battery alert to the wireless system before the battery dies, or may not send the alert at least 7 days in advance as designed. This could leave the call station without power when someone needs to use it.
- 2026-01-14FDA-DeviceSecuritas HealthcareClass IINationwideCheck your Securitas Arial call station battery alerts
A firmware issue in certain Securitas Healthcare Arial 900 MHz call stations (Model CSK200-900) may prevent them from sending low battery warnings to the wireless system. This means the device could lose power without giving you advance notice. The affected units were sold between January 1, 2023 and June 26, 2024.
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