RecallDepth

IDEAL MAXPAC TOTAL SYSTEM (USA) , Sterile and Nonpyrogenic, ETO or Gamma Sterilized, Medtronic Perfusion Systems, Model TS9453R29, TS9453R30, TS1470R1, TS1442R1, TS9800R32, TS8299R4.

Company
Medtronic Inc
Recall Initiated
December 14, 2009
Posted
February 26, 2010
Terminated
April 20, 2011
Recall Number
Z-0868-2010
Quantity
24
Firm Location
Minneapolis, MN

Reason for Recall

Medtronic has identified a small number of Autotransfusion One Source Kits and MAXPAC/Total System lots with incorrect Use Before Dates (UBD) on the outer kit package label. The UBD on the outer label of the kit/pack does not accurately reflect the UBD of the components within the kit/Pack. For affected product, the outer label lists a date which may be later than the USB of the components inclu

Distribution

CA, CO, JAPAN, CHINA.

Lot / Code Info

Lot #: 1058285, 10059556, 1099512, 1106926, 1106983, 1001369.

Root Cause

Incorrect or no expiration date

Action Taken

Consignees were sent a Medtronic "Urgent Medical Device Recall Notice" dated December 14, 2009. The letter was addressed to "Valued Customer." The letter described the product and the problem and requested them to quarantine the product and to complete and sign the attached certificate, "Medtronic Recall Certificate (FCA 1002)." For additional information, contact the firm at 763-514-9605.

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