ClearanceBrief
Recall Z-0359-2024 ยท CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

Instrumentation Laboratory

GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Glucose and Lactate, Part Numbers 00024315009, 00024330009, 00024345009, 00024360009

DateNov 21, 2023 (initiated Sep 29, 2023)
StatusOpen, Classified
ReasonInternal 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.
Root causeUnder Investigation by firm
ActionAn URGENT MEDICAL DEVICE RECALL notification letter dated 9/29/23 was sent to customers. Mandatory Customer Actions Please take the following immediate actions: " Check your inventory for the GEM Premier 3000 Non-iQM PAK (cartridge) lot numbers listed in Appendix A. " Discontinue use and destroy any GEM Premier 3000 Non-iQM PAK (cartridge) lot numbers listed in Appendix A. " Document the destruction on the Mandatory Tracking Response Record and return the completed and signed form to Werfen Regulatory at the fax number or e-mail address listed below. " Contact Werfen Customer Service at 1-800
Quantity2448 units
DistributionUS States: MA, MN, NY. India.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K161818GEM Premier 3000
Instrumentation Laboratory CO, Sep 14, 2016
K992834GEM PREMIER 3000
Instrumentation Laboratory CO, Nov 24, 1999