Hospira Inc. recalls List No. 14207-28; BLOOD SET; 200 Micron Filter, 105 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Ric

Recalled August 14, 2013 · FDA recall Z-1853-2013 · 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

240 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. 14207-28; BLOOD SET; 200 Micron Filter, 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 →