ClearanceBrief
Recall Z-0007-2009 ยท JIY Photometric Method, Iron (Non-Heme)

Roche Diagnostics Corp.

Roche Diagnostics IRON2, Iron Gen. 2, COBAS INTEGRA, cobas c systems, Roche Diagnostics, Indianapolis, IN.; 03183696122. An in-vitro diagnostic reagent system intended for use on COBAS Integra systems for the quantitative determination of iron in serum and plasma.

DateOct 9, 2008 (initiated Jun 11, 2008)
StatusTerminated
ReasonSome of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.
Root causeLabeling Change Control
ActionConsignees were notified via an Urgent Medical Device correction letter dated 6/11/08 informing users of the problem and providing them with work-around instructions. The instructions suggests 1) inserting the cassette rack slowly; 2) using mainly reagent slots A, B, or C; 3) tilting the rack slightly clockwise so the barcode scanner does not read the barcode at an exact 90 degree angle; and 4) confirming the rack is properly seated on the track and displayed on the Cassette Status screen. If the cassette barcode does not register after following the Work-Around instructions, then customers
Quantity523
DistributionNationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K951595ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES
Roche Diagnostic Systems, Inc., Sep 8, 1995