ClearanceBrief
Recall Z-0516-03 ยท FPA Set, Administration, Intravascular

Baxter Healthcare Corp.

Baxter Minivolume Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2C5693; Baxter Healthcare Corporation, Deerfield, IL 60015; 48 units per case

DateFeb 6, 2003 (initiated Oct 17, 2002)
StatusTerminated
ReasonThe I.V. filter sets contain a 1.2 micron filter instead of the labeled 0.22 micron filter.
Root causeOther
ActionRecalled by letter dated 10/17/02. Accounts were informed of the potential for the filters to be 1.2 micron filters instead of the 0.22. micron filters as labeled. The accounts were requested to examine their inventories for the affected catalog numbers and destroy the units found for credit.
Quantity634,992 units
DistributionNationwide, Australia, Puerto Rico, Brazil, Canada, Sweden, New Zealand, Japan, Mexico, American Samoa, El Salvador, Turkey, Saudi Arabia, Austria, Cayman Islands, Macedonia, Honduras, Kuwait, Hong Kong and Nigeria.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K811078RADIATION STERILIZED ADMIN. SET
Travenol Laboratories, S.A., Jul 2, 1981
K924721BAXTER SOLUTION ADMINISTRATION SETS
Baxter Healthcare Corp, Jul 20, 1993