Drug & medication recalls Moderate risk

Diltiazem HCL 1 mg/mL in 0 recalled over sterility concerns

Recall date
June 14, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
SCA Pharmaceuticals, LLC recalls Diltiazem HCL 1 mg/mL in 125 mL 0.9% Sodium Chloride 100 mL bag (total volume 125 mL) (125 mg), SCA Pharmaceuticals, LL…
Recall number
D-0897-2018
FDA classification
Class II
Brand / firm
SCA Pharmaceuticals, LLC
Sold / distributed
Product was distributed throughout the United States.

Why it was recalled

Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.

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

What was recalled

Diltiazem HCL 1 mg/mL in 125 mL 0.9% Sodium Chloride 100 mL bag (total volume 125 mL) (125 mg), SCA Pharmaceuticals, LLC, Windsor, CT

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