FDA Enforcement Class I Terminated

List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, Non-Vented, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration

Recall: Z-1854-2013 · Reported August 14, 2013

Enforcement

Recall Number
Z-1854-2013
Event ID
65689
Classification
Class I
Status
Terminated
Product Type
Devices
Firm
Hospira Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 14, 2013
Initiation Date
April 1, 2013
Classification Date
August 5, 2013
Termination Date
May 24, 2017
Address
275 N Field Dr, N/A, Lake Forest, IL, 60045-2579, United States

Description

List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, Non-Vented, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product Administration

Reason

It was discovered that there was a potential for the piercing pin on certain Hospira blood sets to puncture the outer wall of blood bags during insertion of the pin into the blood bag.

Code Info

List Number: 14210-28; Lot Number: 053835H

Distribution

Worldwide Distribution - USA (nationwide) and Puerto Rico and Internationally to Costa Rica.

Quantity

96 units