Ohio recalls
4745 federal recalls on file affecting Ohio - 760 Ohio-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DrugDaburClass IINationwideMed Pride Hydrocortisone Cream recalled for quality deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideMed Pride antifungal cream recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideMed Pride Bacitracin Zinc Ointment recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideMed Pride Bacitracin Zinc Ointment recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideMed Pride Bacitracin Zinc Ointment recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideCura Hongos antifungal cream recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideRapidol Triple Antibiotic ointment recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideLil Drug Store Triple Antibiotic Ointment recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideCircle K triple antibiotic ointment recalled for manufacturing issues
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideLucky Super Soft antibiotic ointment recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugDaburClass IINationwideLucky Super Soft antifungal cream recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 2026-06-24FDA-DrugInventia HealthcareClass IINationwideInventia Healthcare chlorthalidone tablets recalled for dissolution failure
Failed Dissolution Specifications
- 2026-06-24FDA-DrugSandozClass IIINationwideSandoz Focalin XR 5 mg recalled for labeling error
Labeling: Incorrect or Missing Lot and/or Exp Date
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwideSafco SensiCaine-Ultra topical anesthetic recalled for defective seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwidePureLife benzocaine gel recalled for defective bottle seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwideDental City benzocaine gel recalled for defective container seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwideBurkhart benzocaine gel recalled for incomplete bottle seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwideDHP Topical Anesthetic Gel recalled for incomplete bottle seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwideQuala topical anesthetic gel recalled for incomplete seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugKeystone IndustriesClass IINationwidePearson Quality benzocaine gel recalled for defective seals
Defective container:may contain bottles with incomplete seals
- 2026-06-24FDA-DrugParagon 28Class IINationwidePar Health USA buprenorphine injection recalled for crystallization
Crystallization; identified as Buprenorphine free base
- 2026-06-24FDA-DrugAjanta PharmaClass IINationwideAjanta Pharma aripiprazole recalled for wrong medication inside bottle
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
- 2026-06-24FDA-DrugIntegraDoseClass IINationwideIntegraDose Vasopressin syringes recalled for subpotency
Subpotent Drug
- 2026-06-24FDA-DrugPain Train SalsaClass IINationwideVistaPharm Kerr Insta-Char recalled for failing OTC standards
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- 2026-06-24FDA-DrugPain Train SalsaClass IINationwideVistaPharm Kerr Insta-Char recalled for OTC compliance failure
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- 2026-06-24FDA-DrugPain Train SalsaClass IINationwideVistaPharm Kerr Insta-Char recalled for quality standards failure
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- 2026-06-24FDA-DrugPain Train SalsaClass IINationwideVistaPharm Kerr Insta-Char recalled for not meeting OTC standards
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- 2026-06-24FDA-DrugGlenmarkClass IINationwideGlenmark Alyacen 7/7/7 birth control recalled for impurity levels
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
- 2026-06-18FDA-PRMorningstar FarmsNationwideMorningStar Farms plant-based nuggets and sausage recalled for plastic
CHICAGO, June 18, 2026 – MORNINGSTAR FARMS is voluntarily recalling two varieties of products in the U.S., Puerto Rico and Costa Rica because of possible plastic pieces in the food. Recalled varieties are: MORNINGSTAR FARMS Buffalo Chik’n Nuggets (10.5 oz) and MORNINGSTAR FARMS Hot & Spicy Sausage
- 2026-06-18CPSCCooCooBabyNationwideCooCooBaby baby loungers recalled for suffocation risk
The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.
Get notified about new Ohio recalls
Free weekly digest. Add Ohio to your profile to filter alerts to your state.
Get the Sunday Brief