Hospira Announces Urgent Device Recall

Hospira, Inc. has issued an Urgent Device Recall for certain IV gravity and pump administration sets with CAIR Roller Clamps. The company is voluntarily recalling specific lot numbers of the products, manufactured by Borla S.P.A. of Italy.

If you have purchased ProMed item number 001-11540-58, lot number 600-194W, IV Sets w/Y Injection Site Primary 80" Disp ST (48/cs), during the time period of the recall (since December of 2006), please do a facility-wide search for the product - check every storage room, med room, resident cabinet, etc.

If you locate this product in your facility, it needs to be returned to ProMed immediately. We appreciate your cooperation!