{"data":{"prismicArticle":{"uid":"sun-pharma-cipla-recall-medicines-in-us","tags":["politics"],"first_publication_date":"2026-01-26T11:25:20+0000","last_publication_date":"2026-01-26T11:25:20+0000","data":{"third_party_url":"www.andhraheadlines.com","title":{"text":"Sun Pharma, Cipla recall medicines in US"},"rating":null,"datetime":"2026-01-26T07:36:00+0000","img":{"url":"https://images.prismic.io/prad/aNjogZ5xUNkB1L1e_indpharmatarriffs.JPG?auto=format,compress&rect=0,0,2028,1000&w=2028&h=1000"},"embed":{"embed_url":null,"thumbnail_url":null,"author_url":null,"title":null},"content":{"raw":[{"text":"Indian drugmakers Sun Pharmaceutical Industries and Cipla have recalled certain products from the US market due to manufacturing-related issues, according to the latest update from the US Food and Drug Administration (USFDA). "},{"text":"In its Enforcement Report, the US health regulator said the US-based arm of Mumbai-headquartered Sun Pharma is recalling more than 26,000 bottles of a generic medicine used to treat dandruff and skin conditions that cause inflammation and itching."},{"text":"Sun Pharmaceutical Industries Inc, which is based in Princeton, New Jersey, is recalling 24,624 bottles of Fluocinolone Acetonide Topical Solution after the product failed to meet impurity and degradation standards."},{"text":"The company initiated a nationwide Class III recall in the US on December 30, 2025. The USFDA said a Class III recall is issued in cases where the use of the product is not likely to cause any adverse health effects."},{"text":"The regulator also said Sun Pharma is recalling certain batches of Clindamycin Phosphate USP, a medicine used to treat acne vulgaris."},{"text":"This recall was initiated on November 26, 2025, after test results showed impurity levels and assay values were outside acceptable limits. This recall has also been classified as Class III."},{"text":"Separately, the USFDA said a US-based arm of Cipla has recalled over 15,000 syringes from the American market."},{"text":"Cipla USA Inc, which is headquartered in Warren, New Jersey, is recalling 15,221 pre-filled syringes of Lanreotide Injection due to the presence of particulate matter."},{"text":"Cipla initiated a nationwide Class II recall on January 2 this year. According to the USFDA, a Class II recall is issued when the use of a product may cause temporary or medically reversible health effects, though the chances of serious harm are low."},{"text":"The US remains the world’s largest pharmaceutical market, making regulatory compliance and product quality especially important for drugmakers operating in the country."}]}}},"relatedArticles":{"edges":[{"node":{"uid":"ap-resumes-krishna-water-flow-to-chennai","data":{"third_party_url":null,"title":{"text":"AP Resumes Krishna Water Flow to Chennai"},"img":{"url":"https://images.prismic.io/prad/ah0vFgeQX7-eWd-v_krishnawater.JPG?auto=format,compress&rect=0,0,2026,999&w=2028&h=1000"},"datetime":"2026-06-01T04:06:00+0000"}}},{"node":{"uid":"no-coaching-duty-for-gambhir","data":{"third_party_url":null,"title":{"text":"No Coaching Duty for 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