Heparin 10 Units/ 10 Units in 0 recalled over sterility concerns

Recall date

March 13, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Advanced Pharma Inc. recalls Heparin 10 Units/10 mL 10 Units in 0.45% Sodium Chloride, QS 10 mL, Injectable Solution, Dwell, 10mL Sterile single use…

Recall number

D-1030-2019

FDA classification

Class II

Brand / firm

Advanced Pharma Inc.

Sold / distributed

Nationwide

Why it was recalled

Lack of Assurance of Sterility

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Heparin 10 Units/10 mL 10 Units in 0.45% Sodium Chloride, QS 10 mL, Injectable Solution, Dwell, 10mL Sterile single use syringe, NDC: 42852-725-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404