FDA Drug Recalls

Recalls / Class II

Class IID-588-2013

Product

Proplete 60 - 69 KG (Intradialytic Parenteral Nutrition - dialysate solution with added amino acids), in 555mL bag, Pentec Health Inc, 4 Creek Parkway Suite A Boothwyn, PA 19061-3132

Affected lot / code info
Compounding Date: 04/23/13, 04/24/13, 04/29/13, 05/01/13 Discard after: 05/20/13, 05/22/13

Why it was recalled

Lack of Assurance of Sterility: Sterility could not be assured for compounded sterile renal nutritional prescriptions.

Recalling firm

Firm
Pentec Health
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
4 Creek Pkwy Ste A, N/A, Boothwyn, Pennsylvania 19061-3132

Distribution

Quantity
59 Bags
Distribution pattern
Dialysis Centers Direct to patient

Timeline

Recall initiated
2013-05-15
FDA classified
2013-06-06
Posted by FDA
2013-06-12
Terminated
2014-12-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-588-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.