FDA recall record

American Enterprises LLC dba Sterling Gelatin Limed Bone Gelatin recall — FDA D-062-2013

Microbial Contamination of Non-Sterile Products: Product is being recalled due to possible microbial contamination by C. difficile discovered in the raw…

Class IIclassification
D-062-2013official record ID
Nov 28, 2012report date

Recall record at a glance

Official recordD-062-2013
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAmerican Enterprises LLC dba Sterling Gelatin
Report dateNov 28, 2012
Recall initiation dateSep 21, 2012
Quantity750 kgs
LocationPrince George, VA, United States

Official product description

Limed Bone Gelatin, packaged in six 125 kg fiber drums and labeled in part PO NO.: P8095 GELATIN 75 BLOOM ITEM NO. RM 164. MADE IN INDIA

Why the product was recalled

Microbial Contamination of Non-Sterile Products: Product is being recalled due to possible microbial contamination by C. difficile discovered in the raw material.

Distribution information

NJ

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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