ClearanceBrief
Recall Z-0518-03 ยท FPA Set, Administration, Intravascular

Baxter Healthcare Corp.

Baxter Interlink System Microbore T-Connector Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2N3333; Baxter Healthcare Corporation, Deerfield, IL 60015; 200 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.
Quantity265,240 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

K791496LOW PLASTICIZER ADMINISTRATION SETS
Travenol Laboratories, S.A., Apr 8, 1980
K921899INTERLINK SYSTEM - T-CONNECTOR EXTENSION SET
Baxter Healthcare Corp, Apr 20, 1993
K925126INTERLINK(TM) INJECTION SITE
Baxter Healthcare Corp, Jun 18, 1993