--- title: "Ajanta Pharma USA Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Ajanta Pharma USA Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/ajanta-pharma-usa-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Ajanta Pharma USA Inc recall records **3** reported ongoing 3 records in this archive. Latest source date Aug 25, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 25, 2026 FDA drug enforcement ### [Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-255-01.](https://isitonrecall.com/recall/fda-drug-d-0836-2026-fluphenazine-hydrochloride-tablets-usp-1mg-100-count-bottles-rx-only-marketed-by-ajanta-pharma-usa-i/) 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. Class III Reported ongoing Distribution: Nationwide within the U.S [Official source for Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pha...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22) May 28, 2026 FDA drug enforcement ### [Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by: Ajanta Pharma USA Inc. Bridgewater, NJ 08807, NDC 27241-120-04.](https://isitonrecall.com/recall/fda-drug-d-0611-2026-fenofibrate-capsules-usp-200-mg-rx-only-100-capsules-manufactured-by-ajanta-pharma-limited-india-mar/) CGMP Deviations Class II Reported ongoing Distribution: U.S. Nationwide [Official source for Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0611-2026%22) May 27, 2026 FDA drug enforcement ### [Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-056-03.](https://isitonrecall.com/recall/fda-drug-d-0594-2026-aripiprazole-tablets-usp-rx-only-30-mg-30-tablets-marketed-by-ajanta-pharma-usa-inc-bridgewater-nj-0/) Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg. Class II Reported ongoing Distribution: U.S. Nationwide [Official source for Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridge...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0594-2026%22) ## Reasons in these listed records - 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. - CGMP Deviations - Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg. These examples come from this result page and are not a ranking of every recall reason. ## Checking Ajanta Pharma USA Inc ### Is there a recall on ajanta pharma usa inc right now? This archive contains 3 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Ajanta Pharma USA Inc](https://isitonrecall.com/check/?q=Ajanta%20Pharma%20USA%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)