FDA Drug Recalls

Recalls / Class II

Class IID-0260-2025

Product

Bimatoprost NDC# 82187-1001-1 Container description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping.

Affected lot / code info
Lot Numbers: HABTC0020123, exp. date Dec-2026 HABTC0050623, exp. date May-2027 HABTC0091023, exp. date Sep-2028

Why it was recalled

CGMP Deviations

Recalling firm

Firm
Aspen Biopharma Labs Pvt., Ltd.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
Plot No 10, Biotech Park Phase-II, Lalgadi Malakpet Village,Turkapally, Shameerpet Mandal, Medchal Malkajgiri, N/A, India

Distribution

Quantity
400.0 gm
Distribution pattern
Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)

Timeline

Recall initiated
2025-02-07
FDA classified
2025-03-09
Posted by FDA
2025-03-19
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0260-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.