Maryland recalls
4685 federal recalls on file affecting Maryland - 780 Maryland-specific plus 3905 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-24FDA-DrugDaburClass IINationwideMed Pride Hydrocortisone Cream recalled for manufacturing deficiencies
CGMP Deviations; deficiencies observed during FDA inspection
- 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
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