FDA recall record

Unique Pharmaceutical All sterile products within expiry recall — FDA D-0012-2015

Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic production practices that result in lack of sterility assurance of products…

Class IIclassification
D-0012-2015official record ID
Oct 15, 2014report date

Recall record at a glance

Official recordD-0012-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmUnique Pharmaceutical, Ltd
Report dateOct 15, 2014
Recall initiation dateJul 18, 2014
Quantity325,225 units (syringes, vials, bags)
LocationTemple, TX, United States

Official product description

All sterile products within expiry

Why the product was recalled

Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic production practices that result in lack of sterility assurance of products intended to be sterile.

Distribution information

Nationwide

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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