Maryland recalls
4697 federal recalls on file affecting Maryland - 780 Maryland-specific plus 3917 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 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.
- 2026-06-18CPSCJoolzNationwideJoolz Aer2 Car Seat Adapters recalled for fall hazard
The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall hazard.
- 2026-06-18CPSCSheinNationwideMichley children's pajamas recalled for burn hazard
The recalled children’s pajamas violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death.
- 2026-06-18CPSCArizer TechNationwideArizer Solo III vaporizers recalled for fire risk
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
- 2026-06-18CPSCVeseackyNationwideVeseacky pajama sets recalled for burn hazard
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
- 2026-06-18CPSCArrogantfNationwideArrogantf spa drain covers recalled for entrapment hazard
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to consumers.
- 2026-06-18CPSCGOPO ToysNationwideGOPO Toys teething toy recalled for choking risk
The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's throat and become lodged, posing a serious risk of respiratory distress and deadly choking hazard.
- 2026-06-18CPSCI need more information to accurately identify the consumer-facing brand name for this manufacturer. Huizhou Huitong Crafts Co. Ltd. is a Chinese manufacturer, but without knowing what specific product was recalled or additional branding details, I cannot reliably determine whether this firm operates under the Haitan, Sunhouse, or another brand nameNationwideBABESIDE doll stroller set recalled for choking hazard
The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young children. In addition, the eyes on the plush bear can detach, also posing a choking hazard.
- 2026-06-17FDA-DeviceBoston ScientificClass IINationwideBoston Scientific Orca valve recalled for suction button sticking
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.
- 2026-06-17FDA-DeviceAVID MedicalClass IINationwideHalyard Eye Bag Pack recalled for sterilization failure
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- 2026-06-17FDA-DeviceAVID MedicalClass IINationwideHalyard Drape Pack recalled for unsterilized pouches
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- 2026-06-17FDA-DeviceAVID MedicalClass IINationwideHalyard Towel Six Pack recalled for sterilization failure
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- 2026-06-17FDA-DeviceAVID MedicalClass IINationwideHalyard Pain Pack Kit recalled for unsterilized pouches
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- 2026-06-17FDA-DeviceElektaClass IINationwideElekta MOSAIQ cancer treatment software may fail to load plans
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
- 2026-06-17FDA-DeviceAbbottClass IINationwideAbbott Merlin PCS 3650 programmer software recalled for test termination malfunction
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
- 2026-06-17FDA-DeviceBoston ScientificClass IINationwideBoston Scientific Clik X Anchor recalled for sterility concerns
Sterile anchors my lack sterility assurance.
- 2026-06-17FDA-DeviceBoston ScientificClass IINationwideBoston Scientific TCN Electrodes recalled for performance issues
Reusable electrodes may not meet expected performance levels.
- 2026-06-17FDA-DeviceBoston ScientificClass IINationwideBoston Scientific CSK Electrodes recalled for performance issues
Reusable electrodes may not meet expected performance levels.
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