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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IIMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Major Pharmaceuticals is recalling certain lots of Levothyroxine Sodium Tablets, USP, 75 mcg because they may contain less active ingredient than labeled. Patients taking affected tablets may not receive the full intended dose of this thyroid hormone medication.
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IIMajor Pharmaceuticals levothyroxine tablets recalled for reduced potency
Major Pharmaceuticals is recalling levothyroxine sodium 50 mcg tablets (lot N02200, expiration 10/2026) because they do not contain the full labeled dose. Levothyroxine is a thyroid hormone replacement medication, and a subpotent tablet may not provide the intended therapeutic effect for patients who depend on consistent dosing.
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IIMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Major Pharmaceuticals is recalling one lot of Levothyroxine Sodium Tablets, USP, 25 mcg due to subpotency — meaning the tablets contain less active ingredient than labeled. This affects Lot N02212 with an expiration date of 07/2026. Patients taking subpotent levothyroxine may not receive the full intended dose of this thyroid hormone replacement medication.
- 2026-07-29FDA-DrugPrecision Dose Inc.Not Yet ClassifiedPrecision Dose glycopyrrolate solution recalled for impurity
Precision Dose Inc. is recalling one lot of Glycopyrrolate Oral Solution (1 mg/5 mL) due to an unidentified impurity found during routine stability testing that does not meet specification. The affected lot (506033) expires November 30, 2026. This medication is prescription-only and supplied in unit-dose oral syringes.
- 2026-07-29FDA-PR529 Commerce LLCRooted in Rare Aquafaba Powder recalled for undeclared egg
Rooted in Rare brand Aquafaba Powder may contain undeclared egg, posing a serious allergic reaction risk for people with egg allergies or sensitivities. The recall affects 4 oz and 12 oz packages distributed through Amazon and the company website between June 2025 and July 2026.
- 2026-07-29NHTSA-EquipmentToyota Motor Engineering & ManufacturingToyota side curtain air bags recalled for deployment risk
Certain replacement side curtain air bag assemblies for 2014–2021 Toyota Tundra Double Cab and CrewMax vehicles may have been improperly rolled during manufacturing. This can cause the air bag to deploy incorrectly in a crash, increasing the risk of injury.
- 2026-07-29NHTSA-EquipmentToyota Motor Engineering & ManufacturingToyota Tacoma side curtain air bag recalled for deployment risk
Certain side curtain air bag assemblies sold as replacement parts for 2016–2023 Toyota Tacoma vehicles may not be properly secured to their mounting bracket. This can cause the air bag to deploy incorrectly during a crash, increasing the risk of injury.
- 2026-07-24FDA-PRSunny Pharmtech, Inc.Sunny Pharmtech Cyclophosphamide recalled for steel particles
Sunny Pharmtech is recalling three lots of Cyclophosphamide for Injection (1g and 2g vials) distributed between May 2024 and October 2024 because steel particles were found in the product. No injuries have been reported so far, but steel particles in an intravenous injection could cause serious complications including blood clots and infection.
- 2026-07-24FDA-PRLidl USEridanous Shortbread Cookies recalled for undeclared allergens
Lidl US is recalling Eridanous Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling (11.6 oz box, UPC 4056489125839) because the packaging has foreign language text only and does not clearly list wheat, soy, milk, and egg allergens in English. People with allergies or sensitivities to these ingredients could have serious reactions.
- 2026-07-24FDA-PRBAXTERBaxter Cefazolin Dextrose Injection recalled for particulate contamination
Baxter is recalling one lot of Cefazolin in Dextrose Injection (a frozen antibiotic infusion bag) because cardboard particles were found in the solution. The affected lot (LD175708, expiring February 14, 2027) was distributed between March and June 2025. No injuries have been reported so far.
- 2026-07-24FDA-PRAmerican Regent, Inc.American Regent Papaverine Injection recalled for glass particles
American Regent identified glass and paraformaldehyde particles in one lot of Papaverine Hydrochloride Injection (Lot #25202), a prescription medication used to improve blood circulation and treat muscle spasms. The particles could cause local irritation, blood vessel blockage, and serious complications including stroke.
- 2026-07-24USDAClass IMaple Leaf Foods bacon recalled for import violation
Maple Leaf Foods recalled approximately 12,036 pounds of not-ready-to-eat smoked bacon imported from Canada without required U.S. import reinspection. The affected products are Royale Natural and Top Valu brand uncured bacon packages sold at Grocery Outlet locations in Idaho, Oregon, and Washington, with production dates in June 2026.
- 2026-07-23FDA-PRMidwest Poultry Services. L.P.Midwest Poultry Services eggs recalled for Salmonella risk
Midwest Poultry Services, L.P. is recalling approximately 1.6 million dozen white and brown cage-free shell eggs produced in Texas between June 6 and July 3, 2026, because they may be contaminated with Salmonella Enteritidis. The affected eggs were sold at Kroger, Brookshire's, and other retailers in Texas, Oklahoma, Louisiana, Arkansas, Mississippi, and New Mexico with sell-by dates between July 20 and August 17, 2026. No illnesses have been reported so far.
- 2026-07-23NHTSA-EquipmentK&N Engineering, Inc.Do Not DriveK&N and Spectre fuel filters recalled for fire risk
The O-ring in certain K&N and Spectre replacement fuel filters may disintegrate, causing fuel to leak. A fuel leak near an ignition source can start a fire. Pieces of the O-ring may also clog fuel lines, reducing engine performance and increasing crash risk.
- 2026-07-23CPSCPeony Design Co., of Howell, MIPeony Design baby bibs and stroller bags recalled for choking hazard
Snaps on Peony Design personalized baby bibs and stroller bags can detach, creating a choking hazard for young children. The bibs feature scalloped edges and personalized embroidery, while stroller bags have two snap-closure straps. About 52 items were sold online through Etsy between October 2025 and July 2026.
- 2026-07-23CPSCFoshanshi Kaijinying Dianzishangmao Youxiangongsi (Foshan Kaijinying Electronic Commerce Co., Ltd.), dba YouRfocus, of ChinaCuddleCubs Creations teething toys recalled for choking risk
CuddleCubs Creations teething toy sets sold on Amazon contain pull-string toys with silicone strings that are longer and smaller than safety standards allow. These strings can reach the back of a child's throat and become lodged, creating a serious choking hazard.
- 2026-07-23CPSCShenzhen Yuanxinxiang Trade Co., Ltd., dba Yuanxinxiang, of ChinaOeyUoc pool drain covers recalled for drowning risk
OeyUoc white pool drain covers sold on Amazon do not meet federal safety standards for drain protection and pose a serious risk of entrapment and drowning. The covers violate the Virginia Graeme Baker Pool and Spa Safety Act, which requires drain covers to prevent people—especially children—from getting trapped.
- 2026-07-23CPSCShenzhen Meilanxiang Trading Co., Ltd., dba Sviyatp, of ChinaSviyatp pool drain covers recalled for entrapment risk
Sviyatp white pool drain covers do not meet federal safety standards and pose a risk of entrapment and drowning. The covers were sold online as replacement drain covers for swimming pools from March through June 2026.
- 2026-07-23CPSCShenzhen Aojieni Silicone Technology Co., LTD., of ChinaAojieni Silicone teething toys recalled for choking risk
Aojieni Silicone pull string teething toys have silicone strings that 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 hazard. One child experienced gagging when the strings reached their throat.
- 2026-07-23CPSCXuzhou Mingquanhe Household Co., Ltd., of Changzhou Jiaxuan Intelligence Furniture Co., Ltd., of ChinaRomorgniz fabric dressers recalled for tip-over risk
Romorgniz 12-drawer fabric dressers sold on Amazon are unstable and can tip over if not anchored to a wall, creating a serious injury or death risk to children. The dressers do not meet federal safety standards for clothing storage units.
- 2026-07-23CPSCXuzhou Mingquanhe Household Co., Ltd., of ChinaEnHomee fabric dresser recalled for tip-over risk
EnHomee 9-Drawer Fabric Dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards required for clothing storage units. About 16,800 units were sold online through Walmart.com between September 2023 and March 2026.
- 2026-07-23USDAClass ITasty Kitchen soup recalled for import violation
BCI Foods recalled approximately 4,300 pounds of canned chicken noodle soup imported from Canada because it was not presented for required U.S. import reinspection. The product was distributed to food banks and pantries in Oklahoma. No illnesses have been reported.
- 2026-07-22FDA-DeviceTosoh Bioscience IncClass IITosoh testosterone test recalled for inaccurate results
Tosoh Bioscience recalled certain lots of its ST AIA-Pack Testosterone test due to a quality control issue that can produce falsely high or falsely low testosterone measurements. Inaccurate results may lead to unnecessary follow-up testing or delayed diagnosis.
- 2026-07-22FDA-DeviceDaavlin Distributing CompanyClass IIDaavlin Photera 600 3-D phototherapy device recalled for incorrect UV calibration
The Photera 600 3-D ultraviolet phototherapy device used to treat skin disorders has a calibration error in how it calculates UV output. A sensor setting was incorrectly applied, causing the device to deliver lower UV intensity than intended. This affects 212 units distributed nationwide.
- 2026-07-22FDA-DeviceDaavlin Distributing CompanyClass IIDaavlin Photera 600 phototherapy device recalled for incorrect UV output
The Photera 600 ultraviolet phototherapy device was found to have an error in how it calculates UV output. A sensor setting was incorrect, causing the device to deliver lower UV levels than intended. This affects 26 units with specific serial numbers distributed nationwide.
- 2026-07-22FDA-DeviceDaavlin Distributing CompanyClass IIDaavlin Photera 400 phototherapy device recalled for incorrect UV calibration
The Photera 400 ultraviolet phototherapy device uses a sensor to measure and control UV output for treating skin disorders. A calibration error caused the sensor to report incorrect UV levels, which means patients may have received different doses than intended.
- 2026-07-22FDA-DeviceMaquet Cardiovascular, LLCClass IIMaquet Vasoview Hemopro 2 recalled for sterilization failure
Maquet (now Getinge) identified that 205 units of the Vasoview Hemopro 2 endoscopic vessel harvesting system from a single lot were exposed to an incorrect sterilization dose during gamma sterilization processing. This occurred at a STERIS facility in New Jersey in late March 2026. The affected devices may not be adequately sterilized.
- 2026-07-22FDA-Device3B Medical, Inc.Class II3B Medical Rio II nasal pillows recalled for labeling discrepancy
3B Medical is recalling Rio II nasal pillows interfaces due to a packaging and labeling discrepancy affecting product size identification and device identifiers. The affected units have incorrect or mismatched labeling on certain lots, which could lead to patients receiving the wrong size for their CPAP or PAP therapy device.
- 2026-07-22FDA-DeviceMedtronic Perfusion SystemsClass IIMedtronic Bio-Medicus cannula kit recalled for foreign material
Medtronic received two complaints of loose foreign material inside the Bio-Medicus Adult Cannula Kit used during heart-lung bypass surgery. Testing confirmed the material contained trace levels of blood. No injuries have been reported.
- 2026-07-22FDA-DeviceMedtronic Perfusion SystemsClass IIMedtronic pediatric arterial cannula recalled for foreign material
Medtronic received two complaints of loose foreign material inside the DLP One-Piece Pediatric Arterial Cannula (Product Number 77010), a tube used during heart-lung bypass surgery in children. Testing confirmed the material contained trace levels of blood. No injuries have been reported.