New York recalls
4,048 federal recalls affecting New York in the last 12 months - 418 New York-specific plus 3,630 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-09-23FDA-FoodPanorama ProduceClass IIMartina Fresh Whole Mangoes recalled for Salmonella risk
Panorama Produce Sales Inc. is recalling Martina brand Fresh Whole Mangoes (Lot 038, PLU 4584) because they may be contaminated with Salmonella. The affected mangoes were distributed in Connecticut, New York, New Jersey, and Pennsylvania.
- 2026-09-23FDA-FoodFoods AliveClass INationwideFoods Alive moringa powder recalled for Salmonella risk
Foods Alive organic moringa leaf powder in 8oz pouches may be contaminated with Salmonella. About 1,691 pouches were distributed nationwide and online. No illnesses have been reported so far.
- 2026-09-23FDA-DrugVitruvias TherapeuticsClass INationwideVitruvias Therapeutics thyroid tablets recalled for superpotency
Vitruvias Therapeutics is recalling Thyroid Tablets, USP 1/2 Grain (30 mg) because the tablets are superpotent—meaning they contain higher-than-intended levels of active ingredients. This lot was distributed nationwide. The affected lot number is 504950, expiring 09/30/2026.
- 2026-09-23FDA-DrugPfizerClass IINationwidePfizer Dopamine HCl injection recalled for sterility concern
Pfizer has recalled one lot of Dopamine HCl injection (40 mg/mL) distributed nationwide due to a lack of assurance of sterility. The affected lot is NL5230, with an expiration date of October 2027. This is a precautionary measure to ensure patient safety.
- 2026-09-23FDA-DrugInventia HealthcareClass IINationwideInventia chlorthalidone tablets recalled for dissolution failure
Inventia Healthcare Limited's chlorthalidone 25 mg tablets (batch RISA24002, expiring 04/2027) failed to meet dissolution specifications, meaning the tablets may not break down properly in the body. This could affect how well the medication works. About 13,567 bottles were distributed nationwide.
- 2026-09-23FDA-DrugSun PharmaceuticalClass IINationwideTaro Lidocaine Ointment recalled for strength variation
Taro Pharmaceuticals is recalling one lot of Lidocaine Ointment USP 5% because testing found the active ingredient strength was outside acceptable limits. The affected lot was identified during long-term stability testing. No injuries have been reported.
- 2026-09-23FDA-DrugSafecor HealthClass IINationwideSafecor Health Fluphenazine HCl Elixir recalled for stability failure
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir 20 mg per 4 mL because they failed to meet stability specifications — meaning the medication may not remain safe and effective until its printed expiration date. The affected lots were distributed nationwide.
- 2026-09-23FDA-DrugSafecor HealthClass IINationwideSafecor Health Fluphenazine HCl Elixir recalled for stability failure
Safecor Health is recalling Fluphenazine HCl Elixir (15 mg per 3 mL) in four specific lots because the medication failed to meet stability test requirements. This means the drug may not remain safe and effective through its expiration date. The affected lots were distributed nationwide.
- 2026-09-23FDA-DrugSafecor HealthClass IINationwideSafecor Health Fluphenazine HCl Elixir recalled for stability failure
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir 10 mg per 2 mL because they failed stability testing. This means the medication may not maintain its strength or safety over time. The recall affects 11 lots distributed nationwide.
- 2026-09-23FDA-DrugSafecor HealthClass IINationwideSafecor Health Fluphenazine HCl Elixir recalled for stability failure
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir 5 mg per 10 mL because they failed stability testing requirements. The affected lots may not maintain their expected strength and safety over their labeled shelf life. This medication is used to treat certain psychiatric conditions.
- 2026-09-23FDA-DrugSafecor HealthClass IINationwideSafecor Health Fluphenazine HCl Elixir recalled for stability failure
Safecor Health is recalling multiple lots of Fluphenazine HCl Elixir (5 mg per 1 mL) because the medication failed to meet stability specifications. This means the drug's strength, purity, or safety characteristics may not be reliable. The recall affects 19 lots distributed nationwide.
- 2026-09-23FDA-DrugSafecor HealthClass IINationwideSafecor Health Fluphenazine HCl Elixir recalled for stability failure
Safecor Health is recalling specific lots of Fluphenazine HCl Elixir 2.5 mg per 5 mL because they failed stability testing, meaning the medication may not maintain its strength or safety over time. The affected lots were distributed nationwide.
- 2026-09-23FDA-DrugSun PharmaceuticalNot Yet ClassifiedNationwideSun Pharmaceutical Nystatin Cream recalled for stability failure
Sun Pharmaceutical is recalling specific lots of Nystatin Cream, USP (15 g tubes) because the medication failed stability testing. This means the cream may not maintain its expected strength or safety over time. The affected lots are AD49605 and AD49606, with expiration dates of 05/31/2027.
- 2026-09-23FDA-FoodKraft HeinzNot Yet ClassifiedNationwideHeinz Real Mayonnaise packets recalled for undeclared mustard
Heinz Real - Vraie Mayonnaise 12.5ml single-serving packets contain undeclared ingredients, including mustard. This poses a risk to people with mustard allergies. The affected packets have best-by dates of March 27 or 28, 2027, and were distributed in Canada.
- 2026-09-22USDAA&D FoodsClass INationwideA&D Foods meat products recalled for lack of inspection
Star Meat Delivery Inc. produced approximately 167,639 pounds of raw pork, beef, and goat products without federal inspection and labeled them with a false USDA inspection mark (establishment number EST. 1363). The products were distributed in bulk under the A&D Foods label to retailers and restaurants nationwide. Food produced without inspection may contain harmful bacteria, undeclared allergens, or other contaminants.
- 2026-09-21FDA-PRGlobal MixNationwideNiwali Tejocote Capsules and Pieces recalled for yellow oleander toxicity
Global Mix Inc. is recalling Niwali Tejocote Capsules and Niwali Tejocote Pieces because FDA testing found the products actually contain yellow oleander (Thevetia peruviana), a highly toxic plant. All parts of yellow oleander contain cardiac glycosides that can cause severe or fatal effects including nausea, vomiting, heart rhythm changes, and organ damage.
- 2026-09-18FDA-PRPar HealthNationwidePar Pharmaceutical dexmedetomidine injection recalled for particulate matter
Par Pharmaceutical is recalling two lots of dexmedetomidine HCl injection used in hospitals for patient sedation. The vials contain unwanted particles of cellulose or stopper material that could cause serious blood vessel blockages or clotting if injected into patients. No patient injuries have been reported so far.
- 2026-09-18FDA-PRGF BlendsNationwideGF Blends flour and pizza mixes recalled for undeclared wheat
GF Blends recalled Truly AIP All Purpose Flour and Bread Mix, and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix because they contain undeclared wheat gluten. The contamination came from plantain flour supplied by a third party that tested positive for gluten at levels well above FDA safety limits. People with celiac disease or severe gluten intolerance could experience allergic reactions or other adverse health effects.
- 2026-09-17FDA-PRICU MedicalNationwideICU Medical sodium chloride injection recalled for potassium chloride mix-up
One lot of ICU Medical 0.9% Sodium Chloride Injection (a salt solution) was found to contain 10 mEq Potassium Chloride Injection instead. The vial had the correct outer label but the wrong product inside. This was discovered through a customer complaint.
- 2026-09-17CPSCToyworld168NationwideToyworld168 squishy bun toys recalled for water bead ingestion risk
These translucent green squishy toys contain water beads that expand larger than the legal safety limit. If a child ingests a water bead, it can cause choking, intestinal blockage, vomiting, dehydration, and potentially death.
- 2026-09-17CPSCTongyang CyclingNationwideTongyang Cycling Basecamp helmets recalled for safety failures
Tongyang Cycling's Basecamp model HT-10 bicycle helmets do not meet federal safety standards for impact protection and stability, and may fail to protect your head in a crash. The helmets also contain button cell batteries without required warning labels, creating a poisoning risk if swallowed.
- 2026-09-17CPSCSauna360NationwideSauna360 infrared saunas recalled for fire and burn risk
The infrared heating panels in Sauna360 saunas and kits can short circuit and overheat, creating a risk of fire and serious burns. The company has received 67 reports of overheating, melting, charring, or burning, though no injuries have been reported yet.
- 2026-09-17CPSCSFactorNationwideSauna360 Tylö saunas recalled for collapsing bench hazard
The bench seating in Sauna360's Tylö Halmstad and Kiruna Hybrid sauna rooms can collapse, creating a fall hazard. A previous repair offered in October 2025 did not fully resolve the problem. Sauna360 has received 77 reports of bench failures, resulting in six injuries.
- 2026-09-17CPSCSheinNationwideSHEIN teething toys recalled for choking hazard
SHEIN is recalling Pull and Chew Montessori Teething Toys because the silicone strings are longer and smaller than safety standards allow. The strings can reach the back of a child's throat and become lodged, creating a serious choking risk.
- 2026-09-17CPSCRegfearNationwideRegfear BedsPick mattresses recalled for fire hazard
Regfear's BedsPick brand mattresses (12-inch queen size, sold compressed in boxes) fail to meet mandatory federal flammability standards, creating a risk of fire-related injury or death. The mattresses have a white top with either purple or gray sides and were sold on Amazon between February 2025 and May 2026.
- 2026-09-17CPSCMelissa & DougNationwideMelissa & Doug Fire Truck Activity Board recalled for choking hazard
The black plastic fire hose port on this toy fire truck can come loose and detach, creating a choking hazard for young children. Melissa & Doug has received 26 reports of the port detaching and one report of a minor cut. The toy was sold at Target stores and online from July 2025 through August 2026.
- 2026-09-17CPSCI don't have enough information to match this firm to one of the candidate brands. Ningbo Lanchez E-Commerce Co., Ltd. doesn't directly correspond to Shenyu, Resoul, or Iceberg based on the firm name aloneNationwideLANCHEZ pressure washers recalled for electrocution risk
LANCHEZ-branded electric pressure washers lack a ground-fault circuit-interrupter (GFCI) and have a short power cord, which may lead users to rely on extension cords. This creates a serious risk of electric shock or electrocution. About 329 units were sold online between February and June 2026.
- 2026-09-17CPSCJiande PengshuaiNationwideJKMAX heated blankets and pads recalled for fire hazard
The heating elements inside JKMAX branded heated blankets and pads can overheat, causing the products to smoke, melt, or catch fire. The company has received 577 reports of overheating, including 53 burn injuries.
- 2026-09-17CPSCHaywardNationwideHayward pool heaters recalled for carbon monoxide risk
Hayward-branded HDFS400 Universal-HC Series pool heaters can produce dangerously high levels of carbon monoxide during operation, which may cause serious injury or death. About 4,600 of these 400,000 BTU dual-fuel heaters were sold between March and July 2026.
- 2026-09-17CPSCFriedrichNationwideFriedrich KÜHL window air conditioners recalled for fire risk
The control board inside the motor of certain Friedrich KÜHL Q and KÜHL S window air conditioners can fail, causing the motor to ignite. The company has received two reports of motors catching fire, including one incident that caused smoke and fire damage to a home.
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