Maryland recalls
4792 federal recalls on file affecting Maryland - 784 Maryland-specific plus 4008 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Intro Kit introducer recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP heart pump recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP heart pump recalled for sheath leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP heart pump recalled for sheath leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella 5.5 heart pump recalled for sheath leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella 5.5 heart pump recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Introducer Kit recalled for sheath leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Introducer Kit recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP introducer recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella RP Flex recalled for sheath leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-FoodAmy's KitchenClass IIAmy's Kitchen lentil soup recalled for spoilage risk
Potential for spoilage.
- 2026-07-22FDA-FoodNutriciaClass IINutricia NOURISH meal replacement formula recalled for low vitamin A
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
- 2026-07-22FDA-FoodNutriciaClass IINutricia Liquid Hope formula recalled for low Vitamin A
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
- 2026-07-22FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for packaging seal defect
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
- 2026-07-22FDA-DrugChiesiClass IINationwideChiesi CLEVIPREX injection recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideCAREone Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideMeijer Carbamide Peroxide oral rinse recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideFoster & Thrive Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideLeader Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideGood Neighbor Pharmacy Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideFAMILY Wellness Carbamide Peroxide recalled for subpotent formulation
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideAudiologist's Choice Carbamide Peroxide recalled for low potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideTopCare Health Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideQC Quality Choice Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideClinere Carbamide Peroxide recalled for reduced strength
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideCVS Health Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugPadagisClass IINationwidePadagis Nystatin Cream recalled for reduced potency
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
- 2026-07-21FDA-PRPT OrganicsNationwidePumpkin Tree Peter Rabbit Organics recalled for soft plastic risk
July 21st, 2026, PT Organics Limited of Lake Oswego, Oregon is voluntarily recalling select Pumpkin Tree Peter Rabbit Organics Banana & Strawberry 4 oz. (113 g) pouches because of an internal packaging defect that may result in the presence of a strand of soft, food-grade plastic in the finished pro
- 2026-07-19FDA-PRRelay Peak Research LLCNationwideZen Principle Moringa Capsules recalled for Salmonella risk
Relay Peak Research LLC (Zen Principle Naturals) of Incline Village, NV is voluntarily recalling its Zen Principle® brand Moringa Capsules dietary supplement because the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections i
- 2026-07-18FDA-PRUnique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.)NationwideUnique Pharmaceutical cetirizine tablets recalled for ranitidine contamination
FOR IMMEDIATE RELEASE – July 18th, 2026 – Panoli, Gujarat, Unique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.) is voluntarily recalling four lots of Cetirizine Hydrochloride Tablets USP 5 mg to the consumer level due to cross contamination with Ranitidine.
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