D-1067-2019 Class III Terminated

Recalled by Pfizer Inc. — New York, NY

FDA drug recall D-1067-2019 was initiated by Pfizer Inc. on March 15, 2019 and is designated Class III. Reason for recall: Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point The recall status is terminated (terminated August 11, 2022). Affected quantity: 67 cartons (25 vials per carton).

Recall Details

Product Type
Drugs
Report Date
April 10, 2019
Initiation Date
March 15, 2019
Termination Date
August 11, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
67 cartons (25 vials per carton)

Product Description

Cleocin Phosphate (clindamycin injection), USP, 300 mg/ 2 mL (150 mg/mL), 2 mL-vial, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Pfizer, Inc, New York, NY 10017, NDC 0009-6582-02

Reason for Recall

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Distribution Pattern

Nationwide USA and Guam

Code Information

Lot #: T97469, Exp. 7/2019, W28574, Exp.09/2019