Hospira Inc. Hospira Transpac IV Monitoring Kit, 60 inch disposable transducer monitoring kit with second stopcock by transducer, continuous flush device and drip chamber; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 U.S.A. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hospira Transpac IV Monitoring Kit, 60 inch disposable transducer monitoring kit with second stopcock by transducer, continuous flush device and drip chamber; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 U.S.A.
Brand
Hospira Inc.
Lot Codes / Batch Numbers
list 42584-04-05, lot 35-434-5G
Products Sold
list 42584-04-05, lot 35-434-5G
Hospira Inc. is recalling Hospira Transpac IV Monitoring Kit, 60 inch disposable transducer monitoring kit with second stopcoc due to The I.V. administrations sets were stolen in-transit between the manufacturing site and the sterilizer, resulting in non-sterilized product possibly b. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The 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.
Recommended Action
Per FDA guidance
Hospira 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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
OR
Page updated: Jan 10, 2026