Fexofenadine Hydrochloride Tablets recall — SUN PHARMACEUTICAL INDUSTRIES INC
Failed Impurities/Degradation Specifications
Official ID D-0654-2026 · Official record ↗
6 recent recalls on record for SUN PHARMACEUTICAL INDUSTRIES in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.
Failed Impurities/Degradation Specifications
Official ID D-0654-2026 · Official record ↗
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.
Official ID D-0628-2026 · Official record ↗
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution
Official ID D-0607-2026 · Official record ↗
Presence of Particulate matter: Particulate matter identified as glass.
Official ID D-0580-2026 · Official record ↗
Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
Official ID D-0599-2026 · Official record ↗
Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona
Official ID D-0598-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.