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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.
- 2026-07-01FDA-DrugCareFusion 213, LLCClass IBD ChloraPrep FREPP Clear recalled for sterility concerns
BD ChloraPrep FREPP Clear, a sterile skin antiseptic applicator, may contain fungal contamination (Aspergillus penicillioides) or may not be fully sterile due to wrinkles in the packaging seal. Approximately 178,000 applicators from lot 4073005 (expiring 03/31/2027) are affected nationwide and internationally.
- 2026-07-01FDA-DrugCareFusion 213, LLCClass IBD ChloraPrep Clear recalled for fungal contamination risk
BD ChloraPrep Clear, a sterile antiseptic skin-prep solution used before medical procedures, was found to contain Aspergillus penicillioides fungus in some applicators. This affects the sterility of the product, which is critical for medical use. The affected lot is Lot #4032183 with an expiration date of January 31, 2027.
- 2026-07-01FDA-DrugCareFusion 213, LLCClass IIBD ChloraPrep FREPP Clear recalled for sterility risk
BD ChloraPrep FREPP Clear applicators may have wrinkles in the paper lid that could compromise the sterile seal. This affects multiple lot numbers distributed nationwide through mid-2027. No injuries have been reported.
- 2026-07-01FDA-DrugCareFusion 213, LLCClass IIBD ChloraPrep Clear recalled for sterility assurance concern
BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, is being recalled because wrinkles in the paper packaging lid may allow the sterile seal to be breached. This defect could potentially allow contamination of the product. No injuries have been reported.
- 2026-07-01FDA-DrugPReye LLCClass IIPReye Vitamin See eye drops recalled for sterility concerns
PReye LLC is recalling all lots of PReye Vitamin See Antioxidant Preservative Free Eye Drops due to lack of assurance of sterility. The recall affects approximately 50 to 60 bottles distributed in Colorado. No injuries have been reported.
- 2026-07-01FDA-DrugANI Pharmaceuticals, Inc.Class IIIANI Pharmaceuticals hydroxyzine solution recalled for foreign substance
ANI Pharmaceuticals is recalling hydroxyzine hydrochloride oral solution (10 mg/5 mL, 473 mL bottles) due to the presence of a foreign substance in one lot. The affected product was distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugCentral Admixture Pharmacy Services, Inc.Class IICentral Admixture pediatric TPN bag missing required nutrients
Central Admixture Pharmacy Services issued a recall for one patient-specific Total Parenteral Nutrition (TPN) bag that did not contain copper and famotidine as listed on the label. The bag was prepared for a pediatric patient in Massachusetts. No injuries have been reported.
- 2026-07-01FDA-DrugDirect RxClass IIDirect Rx Duloxetine D/R recalled for impurity risk
Direct Rx's packaged Duloxetine D/R 30 mg capsules contain levels of N-nitroso-duloxetine, a potentially harmful impurity, above FDA's recommended limit. This is a manufacturing quality issue affecting specific lots distributed nationwide.
- 2026-07-01FDA-DrugAmgen, Inc.Class IIAmgen Sensipar cinacalcet tablets recalled for manufacturing deviations
Amgen is recalling Sensipar (cinacalcet) 90mg tablets due to deviations from current good manufacturing practice (CGMP) standards. This affects one lot distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgen, Inc.Class IIAmgen Corlanor recalled for foreign substance contamination
Amgen is recalling specific lots of Corlanor (ivabradine) 7.5mg tablets due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgen, Inc.Class IIAmgen Sensipar tablets recalled for manufacturing deviations
Amgen is recalling Sensipar (cinacalcet) 60mg tablets due to deviations from manufacturing standards. The recall affects one lot (1157055) with an expiration date of January 31, 2028, distributed nationwide.
- 2026-07-01FDA-DrugAmgen, Inc.Class IIAmgen Sensipar recalled for manufacturing quality deviations
Amgen is recalling Sensipar (cinacalcet) 30mg tablets due to deviations from manufacturing quality standards (CGMP). The recall affects one specific lot distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgen, Inc.Class IIAmgen Corlanor heart medication recalled for foreign substance
Amgen has recalled multiple lots of Corlanor (ivabradine) 5 mg tablets due to the presence of a foreign substance in some bottles. The affected tablets are packaged in 14-tablet and 60-tablet bottles distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAjanta Pharma USA IncClass IIAjanta Pharma fenofibrate capsules recalled for quality issues
Ajanta Pharma USA Inc. is recalling one lot of fenofibrate 200 mg capsules due to manufacturing quality deviations discovered during inspection. The affected lot (PA02216, expiring 12/2029) was distributed nationwide.
- 2026-07-01FDA-DrugThe Harvard Drug Group LLCClass IIMajor Pharmaceuticals Methylergonovine Maleate recalled for subpotency
MAJOR Pharmaceuticals is recalling Methylergonovine Maleate Tablets, USP, 0.2 mg due to subpotency — meaning the tablets contain less active ingredient than labeled. The affected lots were distributed nationwide. This is a prescription medication used to control bleeding after childbirth.
- 2026-07-01NHTSA-EquipmentChrysler (FCA US, LLC)Chrysler (FCA US, LLC) - Parking & Daytime Running Lights May Fail/FMVSS 108
Parking lights and daytime running lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.
- 2026-06-30NHTSA-EquipmentNissan North America, Inc.Nissan recalled for instrument panel gear display failure
A hardware failure in certain Nissan transmissions can prevent the instrument panel from displaying which gear the vehicle is in. This missing information increases the risk of a crash.
- 2026-06-26FDA-PRLa Ceiba Foods Latin Market Inc.La Colonia, Selectos Latinos cottage cheese recalled for Listeria risk
La Ceiba Foods is recalling Requesón Salvadoreño (Salvadoran cottage cheese) and Requesón Mexicano (Mexican cottage cheese) sold under the La Colonia, Selectos Latinos, and Clover Hill brands due to possible contamination with Listeria monocytogenes. The contaminated products were distributed to stores and restaurants in Maryland, Virginia, and Washington, D.C. A related outbreak linked to the same dairy manufacturer has caused 12 illnesses and 1 death.
- 2026-06-25FDA-PRRevival Animal Health, LLCBreeder's Edge and Shelter's Choice dog milk replacers recalled for vitamin D risk
Revival Animal Health is recalling several canine and goat milk replacer products because they contain inconsistent levels of vitamin D—some too low, some too high. Dogs fed these products may develop serious health problems ranging from vomiting and weakness to bone deformities (rickets in puppies) or kidney damage (from excess vitamin D). Two cases of rickets have been reported so far.
- 2026-06-25FDA-PRLehi Valley Trading CompanyHigh Valley Orchard raisins recalled for undeclared peanuts
Lehi Valley Trading Company recalled 624 units of High Valley Orchard Chocolate Covered Raisins (15 ounce packages) because they contain undeclared peanuts. The affected product has lot #0160933 and a best-by date of January 23, 2027. A temporary breakdown in production and packaging processes caused the contamination.
- 2026-06-25FDA-PRBear Stewart LLCBakr cookie dough recalled for undeclared soy
Bear Stewart LLC is recalling Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough pouches (lot 2606022) sold at Target in the Southwest because they may contain undeclared soy. The packaging error occurred when S'mores cookies were accidentally packed into Brown Butter Chocolate Chunk pouches. People with soy allergies or sensitivities could have a serious allergic reaction.
- 2026-06-25USDAPublic Health AlertPrivate Selection chicken breast recalled for undeclared eggs
Private Selection Honey Dijon Boneless Skinless Chicken Breasts sold at Kroger and Fred Meyer contain eggs, a known allergen that is not listed on the label. The mislabeling occurred when an incorrect ingredients label was applied to the back of the package. The product is no longer being sold, but some packages may remain in home freezers.
- 2026-06-25USDAPublic Health AlertFresh Seasons Chicken Caesar Wrap recalled for Listeria risk
Fresh Seasons Kitchen Chicken Caesar Wrap products sold at Holiday convenience stores in Minnesota and Wisconsin may contain Listeria monocytogenes bacteria. The contamination was discovered during routine testing; no illnesses have been reported. The affected products were produced on June 16, 2026, and have a "Sell By" date of 6/24/2026.
- 2026-06-25CPSCTreatlife Technology Co. Ltd., of ChinaTreatlife smoke and CO detectors recalled for fire alert failure
Treatlife smoke and carbon monoxide detectors can fail to sound an alarm when smoke or fire is detected. These white, circular detectors are powered by AA batteries and were sold on Amazon. The failure to alert poses a risk of serious injury or death from smoke inhalation or burns.
- 2026-06-25CPSCDaikin Comfort Technologies Manufacturing, Inc., of Houston, TexasAmana air conditioners and heat pumps recalled for fire risk
Certain Amana brand window and through-the-wall air conditioners and heat pumps can experience a ground fault that leaves the heating element energized even after the unit is turned off. This poses a risk of fire or burn injury. One report of plastic melting on a unit has been received, though no injuries have occurred so far.
- 2026-06-25CPSCABGA Advanced Trading Co., Ltd., of Walnut, CaliforniaHonlyne LED party favors recalled for battery ingestion risk
Honlyne LED party favors sold on Amazon contain button cell batteries in compartments that children can easily access and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.
- 2026-06-25CPSCLesonic Technology Co., Ltd., dba Small Fish, of ChinaSmall Fish Busy Board recalled for magnet ingestion risk
Small Fish Montessori Busy Board toys (model 2512JX02) contain magnets that can detach and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injury or death from intestinal perforation, blockage, or infection.
- 2026-06-25CPSCShenzhen Qicheng Trading Co., Ltd., dba Carina and Rambo, of ChinaRaychy light-up children's sneakers recalled for battery ingestion risk
These light-up sneakers contain coin batteries that children can easily access and swallow. Ingesting these batteries can cause serious internal burns and other life-threatening injuries. The sneakers lack required safety warnings and do not meet federal battery safety standards.
- 2026-06-25CPSCShield Line LLC, of Branchburg, New JerseyMedPride Baby Oil recalled for child poisoning risk
MedPride Baby Oil bottles do not have child-resistant caps as required by law. Young children can open the bottle and swallow the oil, which contains petroleum distillates that can cause serious poisoning, chemical pneumonia, and potentially fatal lung damage.
- 2026-06-25CPSCSouthern Telecom Inc., of New YorkVeseacky Lomi waxing kits recalled for burn and fire hazard
The Lomi Roll-On Waxing Kit (models LOMB2003PK and LOMB2004PK) does not meet safety standards for flammability and presents a risk of burns or fire. These handheld wax warmers were sold online through Amazon from October 2020 through January 2026. About 14,700 units are affected.