ClearanceBrief
Recall Z-0504-06 ยท FPA Set, Administration, Intravascular

Hospira Inc.

Hospira Latex Free Blood Secondary Set, 26 inch with Secure Lock; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 U.S.A.

DateFeb 8, 2006 (initiated Jan 9, 2006)
StatusTerminated
ReasonThe I.V. administrations sets were stolen in-transit between the manufacturing site and the sterilizer, resulting in non-sterilized product possibly being on the market.
Root causeOther
ActionHospira notified all of their customers who purchased these list numbers within the last year via letter dated 1/9/06, informing them of the diversion of the affected lots of product prior to being sterilized and that use of the lots could result in the delivery of fluids through a non-sterile pathway. They requested the accounts to check their stocks of the affected list numbers for the list lot numbers. If any of the lots are found in stock, they were requested to place them in quarantine immediately and call Hospira Customer Care at 1-877-946-7747.
Quantity1 set
DistributionThe lots were not released or distributed by Hospira
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K830014HEMA - NV TRANS. BLOOD FILTER 100/800
Abbott Laboratories, Jan 17, 1983