FDA recall record

Mission Pharmacal Co Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit recall — FDA D-1064-2015

Microbial Contamination of Non-Sterile Products: Product failed USP Microbial Limits Test.

Class IIclassification
D-1064-2015official record ID
May 20, 2015report date

Recall record at a glance

Official recordD-1064-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMission Pharmacal Co
Report dateMay 20, 2015
Recall initiation dateApr 30, 2015
Quantity2,412 Kits
LocationBoerne, TX, United States

Official product description

Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit, Rx Only, Sodium Sulfacetamide 9% and Sulfur 4.5% Wash, Net Wt. 16 oz (454 g), Daily Moisturizing Wash, 16 fl. oz. (473 mL), Manufactured for: BioComp Pharma Inc., San Antonio, TX 78230, NDC 44523-0609-23

Why the product was recalled

Microbial Contamination of Non-Sterile Products: Product failed USP Microbial Limits Test.

Distribution information

Nationwide and Puerto Rico

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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