Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL), 250 mL single-dose container recall — FDA D-0390-2025
Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
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Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
Temperature abuse: Wegovy product was potentially exposed to temperatures outside of the products labeled storage conditions due to a shipping error involving a Cardinal Health distribution…
Hyundai Motor America (Hyundai) is recalling certain 2025 Hyundai Palisade vehicles. An insufficient seal on the controller for the electric oil pump may allow moisture to accumulate in the…
Potential contamination with patulin.
Potential contamination with foreign objects.
The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
Glass fragments found in finished product.
The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
Potential contamination with foreign objects.
Undeclared Milk - During an FDA inspection the firm was notified that milk was not declared on the label.
Product does not declare the allergen, milk, on the label.
The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
Undeclared allergen: Wheat
Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during 18-month long term stability…
Lack of Assurance of Sterility: Leaking/damaged syringes.
Superpotent Drug: Assay/potency result for hydromorphone HCl in the compounded stability lot was higher than specification..
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Chrysler (FCA US, LLC) is recalling certain 2017-2019 Jeep Cherokee vehicles. The power transfer unit (PTU) may become damaged and disengage the transmission and differential, resulting in…
General Motors LLC (GM) is recalling certain 2021-2024 Cadillac Escalade and Escalade ESV, Chevrolet Silverado 1500, Suburban, and Tahoe, GMC Sierra 1500, Yukon, and Yukon XL vehicles…
Label declares tahini paste but does not declare sesame.
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