North Dakota recalls
4080 federal recalls on file affecting North Dakota - 175 North Dakota-specific plus 3905 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-22FDA-DeviceOlympusClass IINationwideOlympus Toomey Evacuator recalled for sterilization risk
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical bone marrow tray recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical Arterial Line Kit recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical T-Lok Bone Marrow Tray recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical biopsy kit recalled for sterility failure
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical introducer trays recalled for sterility issue
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 2026-07-22FDA-DeviceArgon Medical DevicesClass INationwideArgon Medical pacing electrode trays recalled for sterility risk
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- 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-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%).
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