Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe,...

FDA Recall #D-0192-2017 — Class II — November 18, 2016

Recall #D-0192-2017 Date: November 18, 2016 Classification: Class II Status: Terminated

Product Description

Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16

Reason for Recall

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Recalling Firm

Cantrell Drug Company — Little Rock, AR

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

1494 syringes

Distribution

Nationwide

Code Information

Lot: 9220

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

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