North Carolina recalls
4656 federal recalls on file affecting North Carolina - 671 North Carolina-specific plus 3985 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-29FDA-DrugRising PharmaClass IINationwideRising Cyproheptadine Hydrochloride Syrup recalled for precipitate
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops recalled for sterility issue
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops recalled for sterility concern
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops Digi Eye recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops Max Strength recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops Max Strength recalled for sterility risk
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugRohto-MentholatumClass IINationwideRohto Cooling Eye Drops recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-29FDA-DrugAscend LaboratoriesClass IINationwideAscend amlodipine-olmesartan tablets recalled for low drug content
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals Levothyroxine 125 mcg recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals Levothyroxine recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for low potency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine recalled for reduced potency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals Levothyroxine 112 mcg recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals Levothyroxine Sodium Tablets recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for reduced potency
Subpotent Drug
- 2026-07-29FDA-DrugMajor PharmaceuticalsClass IINationwideMajor Pharmaceuticals levothyroxine tablets recalled for subpotency
Subpotent Drug
- 2026-07-29FDA-DrugPrecision DoseNot Yet ClassifiedNationwidePrecision Dose glycopyrrolate solution recalled for impurity
Due to an out-of-specification result for an unidentified impurity detected during routine stability testing.
- 2026-07-24FDA-PRSunny PharmtechNationwideSunny Pharmtech Cyclophosphamide recalled for steel particles
July 24, 2026 - Taoyuan City, Taiwan - Sunny Pharmtech, Inc is voluntarily recalling three lots of Cyclophosphamide for Injection, USP, 1g/vial and 2g/vial, to the User Level due to the presence of particulate matter identified as steel. To date, no adverse events or injuries associated with this pa
- 2026-07-24FDA-PRLidlEridanous Shortbread Cookies recalled for undeclared allergens
ARLINGTON, VA – JULY 24, 2026 – Lidl US is recalling all units of Eridanous Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling 11.6 oz (330 g) box UPC 4056489125839 with foreign language ingredients and nutrition facts panel due to undeclared wheat, soy, milk, and egg allergens. Peo
- 2026-07-24FDA-PRBaxterNationwideBaxter Cefazolin Dextrose Injection recalled for particulate contamination
July 24, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling Lot LD175708, Exp 14-Feb 2027 of Cefazolin in Dextrose Injection due to a report of particulate matter found in the solution identified as cardboard.<br> Risk Statement: The use of the defective product has a
- 2026-07-24FDA-PRAmerican RegentNationwideAmerican Regent Papaverine Injection recalled for glass particles
July 24, 2026 – Shirley, NY, American Regent, Inc. is conducting a nationwide voluntary recall of a single lot of Papaverine Hydrochloride Injection, USP, 60 mg/2 mL single dose vial to the consumer level. The product is being recalled due to the presence of particulate matter identified as glass an
- 2026-07-23CPSCPeony DesignNationwidePeony Design baby bibs and stroller bags recalled for choking hazard
The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children.
- 2026-07-23CPSCYouRfocusNationwideCuddleCubs Creations teething toys recalled for choking risk
The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of a child's throat and become lodged, posing a risk of respiratory distress and a deadly choking hazard.
- 2026-07-23CPSCYuanxinxiangNationwideOeyUoc pool drain covers recalled for drowning risk
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to consumers.
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