ClearanceBrief
Recall Z-0958-03 ยท FRN Pump, Infusion

Abbott Laboratories HPD/ADD

I.V. Pump Sets with Cassettes for use with Abbott Plum Series and Lifecare Infusion Pumps; sterile, Rx, single use devices; Abbott Laboratories, North Chicago, IL 60064 USA; 86 different sets listed in the code information section below.

DateJun 27, 2003 (initiated Jun 9, 2003)
StatusTerminated
ReasonThe drip chambers and/or adapters in the sets were manufactured with non-radiation grade plastic resin, resulting in discoloration of the resin.
Root causeOther
ActionThe IV administration sets were recalled by letters dated 6/9/03, advising the accounts of the discoloration of the sight chamber and adapters due to the use of non-radiation grade plastic resin in the manufacture of these components of the sets and requesting the return of the sets for credit. These letters were accompanied by a customer ship history/business reply form, which listed the specific set list numbers and lot numbers shipped to the direct account. The direct accounts were requested to send copies of the enclosed recall letter with the listing of all affected sets to their subacc
Quantity18,413,769 sets
DistributionNationwide and Internationally to Abbott affiliates in Argentina, Aruba, Australia, the Bahamas, Barbados, Bermuda, Bolivia, Brazil, Canada, Cayman Islands, Chile, Columbia, Costa Rica, Croatia, Curacao, Dominican Republic, Ecuador, Egypt, El Salvador, France, Greece, Guam, Guatemala, Haiti, Hondura
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K832755INFUSION PUMP & IV SETS #4000
Omni-Glow, Inc., Nov 3, 1983
K865059I.V. SET W/SINGLE-CHANNEL CASSETTE
Abbott Laboratories, Feb 6, 1987
K865060I.V. SET WITH DUAL-CHANNEL CASSETTE
Abbott Laboratories, Feb 6, 1987
K920736IVEX-HP96 EXTENDED LIFE FILTER SET
Abbott Laboratories, Apr 23, 1993
K941214LIFESHIELD EXTENSION SET
Abbott Mfg., Inc., Oct 3, 1994