Ajanta Pharma USA Inc recalls
2 notices naming Ajanta Pharma USA Inc in the last 60 days, newest first. The name is the one FDA gives to the recalling firm.
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Hazard and remedy text is quoted from the agency, unedited. The red tag names the kind of risk with a word from that text. Every notice links to its official page.
Quality defect
Ajanta Pharma USA Inc: Ranolazine Extended-Release Tablets
Hazard (FDA): Failed Dissolution Specifications: below specification
FDAMedicines
Quality defect
Ajanta Pharma USA Inc: Fluphenazine Hydrochloride Tablets
Hazard (FDA): Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent.
FDAMedicines
For recalls older than this period, search U.S. Food and Drug Administration (opens in a new tab).
Questions about Ajanta Pharma USA Inc recalls
How many Ajanta Pharma USA Inc recalls are listed?
2 notices naming Ajanta Pharma USA Inc were published by FDA in the 60 days before October 13, 2026, in: medicines. Older recalls of the firm are on the site of the agency.
What is the most recent Ajanta Pharma USA Inc recall?
“Ajanta Pharma USA Inc: Ranolazine Extended-Release Tablets”, published on October 7, 2026. FDA describes the hazard as: “Failed Dissolution Specifications: below specification”
I own a Ajanta Pharma USA Inc product. Is it recalled?
Only if it matches the model, lot or date codes on one of the notices. Open the notice and compare the codes with the ones printed on your product; the brand alone is not enough.
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