FDASeptember 29, 2023device

GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Part Numbers 00024307504, 00024330004, 00024345004

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled performance specifications for pO2. The positive bias may lead to false positive for medical decision levels at pO2 < 60 mmHg, which may result in failure to detect and/or adequately treat hypoxemia and lead to a delay in treatment. The quality control procedures for the Non-iQM GEM Premier 3000 may not detect the non-conformance.

What to do

FDA enforcement status: Ongoing

Brands named

instrumentation laboratoryinstrumentation

UPCs

000243075040842695008792200024330004084269500825070002434500408426950082538

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Part Numbers 00024307504, 00024330004, 00024345004 — Recall Details · AllClear