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

Recall Z-3081-2024 — GE Panda iRES Warmer, Model/Catalog Numbers: 1) M1112198-01045518; 2) M1112198-01045579; 3) M1112198-01047148; 4) M1112198-01047271; 5) M1112198-01048731; 6) M1112198-01048740; 7) M1112198-01052386; 8) M1112198-01054697; 9) M1112198-01068942; 10) M1112198-01084972; 11) M111219

U.S. FDA — Device Enforcement · India · 2024-08-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3081-2024
Date of alert
2024-08-09
Country / jurisdiction
India
Risk level
Class II
Risk type
recall
Brand
Wipro GE Healthcare Private Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
01045518
Reported risk: GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing of certain Giraffe and Panda iRes Warmers. There are multiple electrical safety protections included in the product design. However, because the electrical safety testing in manufacturing was incomplete for these devices, there is the potential for leakage current to exceed IEC 60601 limits.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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