ClearanceBrief
Recall Z-0553-06 ยท MEA Pump, Infusion, Pca

Baxter Healthcare Corp.

Baxter PCA II Syringe Infusion Pump, product codes 2L3104 and 2L3104R; Baxter Healthcare Corporation, Deerfield, IL 60015

DateApr 26, 2006 (initiated Dec 21, 2005)
StatusTerminated
ReasonDelivery of unrequested PCA doses of medication due to damaged PCA cords, partial sticking of PCA button, and fluid ingress into the pump or PCA button.
Root causeOther
ActionBaxter sent Urgent Device Correction letters dated 12/21/05 to the direct accounts on the same date via first class mail. The letters informed the accounts of the potential for unrequested PCA doses due to an electrical short in the PCA circuit simulating repeated pressing of the PCA button. The unrequested bolus doses will not exceed the programmed prescription limits. The letter listed three conditions identified that can produce an electrical short in the PCA circuit and simulate repeated pressing of the PCA button: * Damaged PCA cord or button, * Partial sticking of the PCA button, and *
Quantity30,000 pumps
DistributionNationwide including Puerto Rico, and internationally to Canada, Chile, China, Hong Kong, Korea, Kuwait, Malaysia, Taiwan and Saudi Arabia
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K880733BARD PCA II INFUSION PUMP
C.R. Bard, Inc., Jun 20, 1988
K902613BARD PCA II PUMP WITH PROGRAM CARTRIDGES
C.R. Bard, Inc., Apr 19, 1991
K914502BARD PCA II PUMP WITH PROGRAM CARTRIDGES
C.R. Bard, Inc., Dec 18, 1991
K921994BARD PCA II PUMP WITH PROGRAM CARTRIDGES
C.R. Bard, Inc., Aug 3, 1992