FDA recall D-589-2013

Pentec Health · Class II · drug

Product

Proplete 70+ KG (Intraperitoneal Parenteral Nutrition - dialysate solution with added amino acids), in a) 635mL bag and b) 660mL bag, Pentec Health Inc 4 Creek Parkway Suite A Boothwyn, PA 19061-3132

Reason for recall

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

Distribution

Dialysis Centers Direct to patient

Key facts

Status
Terminated
Initiation date
2013-05-15
Report date
2013-06-12
Termination date
2014-12-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Boothwyn, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-589-2013