Hospira Inc. recalls List No. 14210-28; PLUM BLOOD SET; 100 mL Burette with Prepierced Injection Site, 170 Micron Filter, Prepierced Port, No

Recalled August 14, 2013 · FDA recall Z-1854-2013 · Hospira

Hazard

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. · FDA Class I

Units

96 units

Sold at

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

Description

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.

Product

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

Manufacturer(s)

Hospira Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →