← FDA ENFORCEMENT
D-0490-2024Class III

Acella Pharmaceuticals, LLC

Recalling firm
Acella Pharmaceuticals, LLC
Product type
Drug
Status
Terminated
Report date
2024-05-15
Distribution
Nationwide in the US and Puerto Rico.
Firm state
GA
Product quantity
7104 Bottles
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason for recall

Subpotent drug

Product description

Sodium Sulfacetamide 10% - Sulfur 5% Cleanser, Rx Only, 6 oz (170.3 g) Bottle, Manufactured for Acela Pharmaceuticals, LLC Alphareta, GA 30005, NDC 42192-136-06

Code / lot info

Lot # 22085 Exp. date 08/02/2024

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See all Validation & Qualification recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.