GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Part Numbers 00024307507, 00024315007, 00024330007, 00024345007, 00024360007
FDA Recall Z-0358-2024 · Posted 2023-11-21
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Recalling FirmInstrumentation Laboratory
Recall StatusOpen, Classified
Product CodeCHL
Date Initiated2023-09-29
Product Quantity2448 units
Reason for Recall
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.
Firm Action
An 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 1-800-955-9525 to order replacement PAKs (cartridges).
" Share this information with your laboratory staff and follow your internal procedures.
" Forward this notification to all affected locations within your facility.
" Retain a copy of this notification for your records.
Mandatory Response Tracking Record
" Return the completed and signed Mandatory Response Tracking Form to:
" Fax No.: 1-781-861-4207
Or
" E-mail: [email protected]
Contact Information for Questions
" For technical questions, contact the Technical Support Center at 1-800-678-0710.
" For replacement cartridges, contact Customer Service at 1-800-955-9525.
Root Cause
Under Investigation by firm
Distribution Pattern
US States: MA, MN, NY. India.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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