medical Class II Updated 2019-10-30

Abbott Laboratories recalls Emerald Diluent Tubing, List number 09H50-01, accompanying C

Recalled Product

Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald instrument, List number 09H39-01. The firm name on the label is Abbott Laboratories, Abbott Park, IL.

Hazard / Issue

The diluent tubing used on the instrument appears cloudy or to have a powder/film on the inner and outer surfaces which may result in falsely elevated platelet results.

Issued by

FDA

Affected States: GA, LA, MA, NC, NY, SC, TX

Lot/Code Info: Tubing lot #2018-10-16; Instrument serial numbers 007689, 007690, 007691, 007692, 007705, 007706, 007707, 007708, 007709, 007728, 007694, 007695, 007697, 007766, 007767, 007768, 007765, 007710, 007699, 007700, 007701, and 007703.

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