ONE SOURCE PACK, Model TK2S24, EE2S048 (OUS), Manufacturer: Medtronic, Inc., Minneapolis, MN 55432-5604.
- Company
- Medtronic Inc
- Recall Initiated
- December 14, 2009
- Posted
- February 26, 2010
- Terminated
- April 20, 2011
- Recall Number
- Z-0869-2010
- Quantity
- 12
- 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 #: 1093645, 1102929, 1139554
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.