All recalls
- 2026-03-04FDA-FoodTENGEN USA TRADING CORPClass IIIYO!MAN CUCUMBER (FRESH HUNAN FLAVOR); Ingredients: Cucumber, chili pepper, edible vegetable oil, salt, water, sugar, brewing vinegar, food additives (monosodium glutamate, sodium dehydroacetate, potassium sorbate, streptoccoccus lactis, sodium D-isoacsorbate, disodium ethylenediaminetetraacetatic acid, sodium metabisulphite, citric acid, lactic acid, glacial acetic acid, xanthan gum), food flavors and fragrances; NET WT. 4.42oz.(125g); SHELF LIFE: 10 MONTHS; PRODUCT OF CHINA; Distributed by: Ten
Product contains undeclared cyclamates.
- 2026-03-04FDA-FoodLUBNA QUALITY PRODUCTS INC.Class IIIMung Beans packaged in 4lb polybags; 6-4lb bags per carton
Presence of Thiamethoxam-PESTICIDE
- 2026-03-04FDA-FoodJ2C Hawaii LLCClass IITiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label is read in parts: ***INGREDIENTS: Sugar***Whey Powder, Nonfat Milk Powder, Soy Lecithin***Peanut Butter (peanuts, peanut oil***), Pretzels (wheat flour***buttermilk solids***CONTAINS MILK AND SOY ***May contain wheat, peanuts and tree nuts***"
Ingredients List declares peanut but the Contains statement does not declare peanut
- 2026-03-04FDA-FoodOregon Potato Company LLCClass IIQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged in polyethylene liner within a Gaylord 1400lbs. tote. Product was not sold to consumers from retail stores. Willamette Valley Fruit Company 2994 82nd Ave. NE Salem OR 97305
Listeria monocytogenes
- 2026-03-04FDA-FoodPrime Food Processing LLC.Class IPrime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER FISH); DISTRIBUTED BY: PFP LLC, Brooklyn, NY, 11211, USA; Product must be thoroughly cleaned and cooked before consumption.; PRODUCT OF VIETNAM; UPC: 6 946976 818000
Uneviscerated Fish
- 2026-03-04FDA-FoodGerber Products Company dba Nestle Infant NutritionClass IIGerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015000005962, packed 4 bags/case with UPC 015000935726; Made for Gerber Products Co., Fremont, MI 49413
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IIBioGlo Fluorescein Sodium Ophthalmic Strips USP, 100 diagnostic strips, Manufactured by Omni Lens PVT. Ltd., 5 - Samrudhhi, Opp. Sakar-III, Navrangpura, Ahmedabad, Gujarat, India - 380014, Email:info@omnilens.in, Manufactured for & disibruted by: HUB Pharmaceuticals, LLC, 8767 E Via de Ventura #175, Scottsdale, AZ, 85258, NDC 17238-900-11.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IIBio Glo Fluorescein Sodium Ophthalmic Strips USP, 300 diagnostic strips, Manufactured Omni Lens Pvt Ltd 5 - Samruddhi, Opp. Sakar - III, Navrangpura, Ahmedabad - 380014, India, Email:info@omnilens.in, Manufactured for & distributed by: HUB Pharmaceuticals, LLC, 8767 E Via de Ventura #175, Scottsdale, AZ, 85258, NDC 17238-900-30.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IICHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) 100-count box, NDC 83851-100-10; b) 300-count box, NDC 83851-100-30. Manufactured by Wizcure Pharmaa PVT. LTD, H-681, Phase 3, RIICO Industrial Area, Bhiwadi- 301019 INDIA, Vistamerica USA, 20 Perkins Dr. Prescott, AZ 86301, Vistamerica USA, Made in India,
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IIVista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops. Dry Eye Relief, 15 ml. (1/2 fl. oz.), Wizcure Pharmaa Pvt. Ltd., H-881, Phase-3, RIICO Industrial Area, Bhiwadi-901019, INDIA, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-022-15.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IIVista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Dry Eye Relief Revitalizing Formula, 10 ml (1/3 fl.oz.), Wizcure Pharmaa PVT. LTD., H-881, Phase 3, RIICO Industrial Area, Bhiwadi-301019, India, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ 85260, NDC 77790-003-10.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IIVista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. (1/3 fl. oz), Wizcure Pharmaa PVT. LTD, H-881, Phase-3, RIICO Industrial Area, Bhiwadi-301019, India, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-002-10.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugWizcure Pharmaa Private LimitedClass IIVista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops, Dry Eye Relief, Lubricant Drops, Sterile 10 ml (1/3 fl. oz.), Manufactured by: RA/Drugs/ MFG/2019/196283, Omni Lens Pvt. Ltd. 5, Samrudhhi, Opposite:Sakar-III, Navrangpura, Ahmedabad-380014, INDIA. Manufactured for and distributed by hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260. NDC 77790-001-10.
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
- 2026-03-04FDA-DrugAgeboxClass IIAgebox iKids-Growth (Night Formula), 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 850065597027
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
- 2026-03-04FDA-DrugAgeboxClass IIAgebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
- 2026-03-04FDA-DrugSlate Run PharmaceuticalsClass IIIEptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only, Manufactured by: Hainan Poly Pharm. Co., Ltd., Guilinyang Economic Development Area, Haikou, Hainan Province, China 571127; Distributed by: Slate Run Pharmaceuticals, LLC, Columbus, Ohio 43215. NDC Slate Run Carton Label: 70436-027-80; NDC ProRx Carton Label: 70436-163-80
Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.
- 2026-03-04FDA-DrugAvKAREClass IIAmantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
- 2026-03-04FDA-DrugLEO PHARMA INCClass IIAdbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only, Manufactured by: LEO Pharma A/S. Industriparken 55, DK-2750 Ballerup, Denmark, Distributed by: LEO Pharma Inc., Madison, NJ 07940, USA,
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.
- 2026-03-04NHTSA-EquipmentKumho Tire Co., Inc.Kumho Tire Co., Inc. — Tire Tread May Separate/FMVSS 139
Tread separation may increase the risk of a crash.
- 2026-03-03USDAClass IAjinomoto Foods North America, Inc. Expands Recall for Chicken and Pork Fried Rice, Ramen, and Shu Mai Products Due to Possible Foreign Matter Contamination
Product Contamination
- 2026-03-01USDAPublic Health AlertFSIS Issues Public Health Alert for Ready-To-Eat Beef Jerky Products Due to Misbranding and Undeclared Allergen
Unreported Allergens
- 2026-02-26CPSCShenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of ChinaEvajoy Above-Ground Pools 48 Inches and Taller Recalled Due to Drowning Hazard; Manufactured by Shenzhen Danya Tech
The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.
- 2026-02-26CPSCHisense Ltd., of IsraelBabysense Max View Baby Monitors Recalled Due to Fire Hazard; Manufactured by Hisense
The display or "parent" unit of the Max View baby monitors can overheat and/or spark when charging, posing a fire hazard to consumers.
- 2026-02-26CPSCAndersen Windows, Inc., of Bayport, MinnesotaAndersen Windows Recalls Window Opening Control Devices Sold as Kits or Installed on 100 Series Casement Windows Due to Fall and Serious Injury Hazards
The window opening control devices can break or detach after accidental or other impact, allowing the window to be opened, posing fall and serious injury hazards.
- 2026-02-26CPSCDongguan Fuxin E-Commerce Co., Ltd., dba SumDirect, of ChinaSumDirect LED Mini Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-02-26CPSCTodson, Inc., of Foxboro, MassachusettsTodson Recalls Concord Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system and positional stability requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- 2026-02-26CPSCGuangzhou Mengli Trading Co., Ltd., dba Indream Store, of ChinaJoyreal Busy Board Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking and Laceration Hazards; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Indream Store
The recalled children's toys violate the small parts ban because the small mirror can detach from the toy, posing a deadly choking hazard. In addition, the toys violate the mandatory standard for toys because the toy's mirror has sharp edges, posing a laceration hazard.
- 2026-02-26CPSCShenZhenShiGuWangChuanShuoKeJiYouXianGongSi (Shenzhen Guwang Legend Technology Co., Ltd.), dba n b plus, of ChinaZelbuck Children's Chess Games Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by n b plus
The recalled children's chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, they can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Sensory Swing Due to Risk of Serious Injury or Death from Strangulation
The recalled swing's flexible fabric can form loops that can entangle a child's head or neck, posing a risk of serious injury or death from strangulations.
- 2026-02-26CPSCSN Commerce LLC, dba TheKiddoSpaceStore, of Dover, DelawareTheKiddoSpace Recalls Children's Christmas Tree Play Sets Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban and Mandatory Standard for Toys
The zipper pull on the music box compartment of the recalled Christmas Tree Toys contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues. Additionally, the Christmas tree component fails to comply with various mechanical and electrical requirements for battery-operated toys.