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U.S. Department of Health and Human Services

Class 2 Device Recall Hospira Transpac IV Monitoring Kit

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 Class 2 Device Recall Hospira Transpac IV Monitoring Kitsee related information
Date Initiated by FirmJanuary 09, 2006
Date PostedFebruary 08, 2006
Recall Status1 Terminated 3 on July 20, 2006
Recall NumberZ-0506-06
Recall Event ID 34354
510(K)NumberK813464 K831506 
Product Classification Set, Administration, Intravascular - Product Code FPA
ProductHospira 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.
Code Information list 42584-04-05, lot 35-434-5G
Recalling Firm/
Manufacturer		 Hospira Inc.
275 N Field Dr
Lake Forest IL 60045-2579
For Additional Information ContactLuann M. Pendy, PhD
224-212-2000
Manufacturer Reason
for Recall		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.
FDA Determined
Cause 2		Other
ActionHospira 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.
Quantity in Commerce60 sets
DistributionThe lots were not released or distributed by Hospira
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = FPA
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