FDA recall record

Pharmakon Pharmaceuticals Promethazine 25 mg added to 0.9% Sodium Chloride 50 mL fill in a recall — FDA D-1276-2016

Lack of Assurance of Sterility

Class IIclassification
D-1276-2016official record ID
Jul 20, 2016report date

Recall record at a glance

Official recordD-1276-2016
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPharmakon Pharmaceuticals, Inc.
Report dateJul 20, 2016
Recall initiation dateApr 20, 2016
Quantity485
LocationNoblesville, IN, United States

Official product description

Promethazine 25 mg added to 0.9% Sodium Chloride 50 mL fill in a 100 mL B/Braun PAB bag, Rx, Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0187-41

Why the product was recalled

Lack of Assurance of Sterility

Distribution information

Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA

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: Press Release.

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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