D-1071-2017 Class II Terminated

Recalled by Cantrell Drug Company — Little Rock, AR

FDA drug recall D-1071-2017 was initiated by Cantrell Drug Company on July 14, 2017 and is designated Class II. Reason for recall: Lack of Sterility Assurance. The recall status is terminated (terminated September 16, 2020). Affected quantity: 1718 bags.

Recall Details

Product Type
Drugs
Report Date
August 16, 2017
Initiation Date
July 14, 2017
Termination Date
September 16, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1718 bags

Product Description

Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 mL (64 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-288-18

Reason for Recall

Lack of Sterility Assurance.

Distribution Pattern

Nationwide within the US

Code Information

Lot 3:: 10374, BUD: 8/4/2017; 10429, BUD: 8/13/2017; 10532, BUD: 8/27/2017