New Mexico recalls
3300 federal recalls on file affecting New Mexico - 224 New Mexico-specific plus 3076 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Sambhar Mix KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Methi Blocks KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Karela Ring Cut KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Kantola KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Guvar KEEP FROZEN a) Net Wt. 12 oz. (340 g); b) Net Wt. 2 LB (907 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Chikoo Slices KEEP FROZEN Net Wt. 12 oz. (340 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Baby Bhindi KEEP FROZEN Net Wt. 12 oz (340 g)
Product tested positive Salmonella .
- 2025-12-17FDA-FoodChetakClass INationwideDeep-brand Premium Select Surti Undhiu Mix Net Wt. 12 oz. (340 g) KEEP FROZEN
Product tested positive Salmonella .
- 2025-12-17FDA-FoodByHeartClass INationwide1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets
Contaminated with Clostridium botulinum
- 2025-12-17FDA-DrugLupinClass IINationwideSertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.
Defective container - seal not adhering to bottles
- 2025-12-17FDA-DrugCiplaClass IINationwideCinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-412-02
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- 2025-12-17FDA-DrugCiplaClass IINationwideCinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-411-02
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- 2025-12-17FDA-DrugCiplaClass IINationwideCinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-410-02
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- 2025-12-17FDA-DrugWinder LaboratoriesClass IIINationwideMorphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL, Rx Only, For Oral Use Only, Manufactured By: /winder Laboratories, LLC, Winder, GA 30680. NDC: 75826-131-01
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
- 2025-12-17FDA-DrugGlenmarkClass IIINationwideNebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for Avkare, Pulaski, TN 38478, Product of Italy, NDC 42291-874-90.
Cross Contamination with Other Products
- 2025-12-17FDA-DrugFagronClass IINationwideTropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution, 0.5mL Single-Use Syringe, For Topical Ophthalmic Use Only. Not for IV Use. Fagron Sterile Services, 8710 E 34th St N, Wichita, KS 67226. NDC: 71266-8240-01
Incorrect Product Formulation
- 2025-12-17FDA-DrugDr. Reddy'sClass IIINationwideVarenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-908-56
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.
- 2025-12-17FDA-DrugCiplaClass IINationwideLanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., (a subsidary of Cipla Ltd) Hauppauge, NY 11786, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33422, Carton NDC 76282-478-90; Bottle NDC 76282-478-13.
Failed stability specifications: Out of specification for hardness test
- 2025-12-17FDA-DrugCiplaClass IINationwideLanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., Hauppauge, NY 11786, Manufactured for : Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-936-98.
Failed stability specifications: Out of specification for hardness test
- 2025-12-12USDAClass INationwideDo not serve Suzanna's Kitchen breaded chicken
Misbranding, Unreported Allergens
- 2025-12-11CPSCYongkang Luyuan Industrial & TradingNationwideLuyuan Recalls Youth ATVs Due to Risk of Serious Injury or Death from Crash Hazard; Violate Mandatory Standard for All-Terrain Vehicles
The recalled youth ATVs violate the mandatory ATV safety standard. The youth ATVs' mechanical suspension fails to comply with safety requirements, posing a crash hazard. Additionally, the handlebars pose a laceration hazard, if the child rider's body or head impacts the handlebars at high speed. ATVs that fail to meet the mandatory safety requirements pose a risk of serious injury or death.
- 2025-12-11CPSCVevorNationwideSanven Technology Recalls Vevor Ice Crushers Due to Fire Hazard
The ice crusher can experience a thermal event and ignite, posing a fire hazard.
- 2025-12-11CPSCBenTalkNationwideYCXXKJ Baby Bath Seats Recalled Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats; Sold on Amazon by BenTalk
The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
- 2025-12-11CPSCVevorNationwideSanven Technology Recalls VEVOR Steamers Due to Risk of Serious Injury from Burn Hazard
The steamers can leak or spit hot water, posing a risk of serious burn injury to users and bystanders. The water tank cap can also leak or detach during use, exposing users to hot water.
- 2025-12-11CPSCBaoDNationwideUuoeebb Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by BaoD
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard. In addition, the infant walkers have leg openings that allow the child to slip down until the child's head can become entrapped, posing a risk of serious injury or death.
- 2025-12-11CPSCSKCAIHT DirectNationwideSKCAIHT Children's Costumes Recalled Due to Risk of Injury from Phthalate Exposure; Violates Federal Phthalates Ban; Sold on Amazon by SKCAIHT Direct
The children's costumes contain a prohibited phthalate, which violates the federal phthalates ban. Phthalates are toxic if ingested by young children and can cause adverse health effects.
- 2025-12-11CPSCTrekNationwideTREK Recalls Electric Bicycles Due to Fall or Crash Hazard
The bolts on the chainring can come loose, causing the chainring to separate from the bike, resulting in a fall or crash hazard to the user.
- 2025-12-10FDA-DeviceIlluminaClass IINationwideReagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5 (75 cycles) IVD, REF: 20028870/NextSeq 550Dx HO FC Cart v2.5, 75 Cycles, REF: 20031098; NextSeq 550Dx High Output Reagent Kit v2.5 (300 cycles) IVD, REF: 20028871/NextSeq 550Dx HO FC Cart v2.5, 300 Cycles, REF: 20026365; CN NextSeq 550Dx High Output Reagent Kit v2.5 (75 cycles) IVD, REF: 20064341/CN NEXTSEQ 550Dx HO FLOW CELL V2.5, REF: 20062316; CN NextSeq 550Dx High Outpu
An instrument intended for sequencing DNA libraries with in vitro diagnostic assays is used with reagent kits including flow cells that have flow cell gaskets that have a quality issue, which may lead to flow cell leaks during runs, which could cause run failures, that may result in: No/insufficient data output, instrument fluidics clogs, toxic substance exposure to user.
- 2025-12-10FDA-DevicePhilipsClass IINationwideLumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
- 2025-12-10FDA-DevicePhilipsClass IINationwideCT 5300; Software Version Number: 4.5, 5.0, 5.1;
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make contact with other components located within the Incisive CT systems during rotation. Other components could be damaged due to the contact with the tube heat exchanger.
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