FDA Recall D-0358-2019

Lupin Pharmaceuticals Inc. · Baltimore, MD

Class I — life-threatening Terminated 607 days on record

Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death.

Product

Ceftriaxone for Injection USP, 2 g, packaged in 10 Single Use Vials (NDC 68180-644-01) per box, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-644-10.

Lot / code: Lot #: C600109, Exp 05/19; C600129, C600135, Exp 08/19

Quantity: 3,792 boxes

Reason for recall

Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.

Recall record

Recall number: D-0358-2019
Classification: Class I
Status: Terminated
Voluntary or mandated: Voluntary: Firm initiated
Firm notification: Letter
Distribution: Nationwide in the USA and Puerto Rico.
Recall initiated: 2018-12-20
Classified by FDA Center: 2019-01-14
FDA published: 2019-01-16
Terminated: 2020-08-18
Recalling firm: Lupin Pharmaceuticals Inc.
Firm location: Baltimore, MD

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