Cipla USA, Inc.: Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled
Recall reason: Presence of Particulate Matter.. Recalled by Cipla USA, Inc.. Distribution: Nationwide in the USA. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot, expiry: 4301954IR1 , exp 31/10/2026 ; 4301994IR1 , exp 31/10/2026 ; 4301995IR1 , exp 31/10/2026 ; 4301996IR. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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