Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1535-2026 — GEM Premier 5000; Part No. 00055415010.

U.S. FDA — Device Enforcement · United States · 2026-01-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1535-2026
Date of alert
2026-01-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Instrumentation Laboratory
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00055415010
Reported risk: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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