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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