Maquet Inc KION Anesthesia System. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
KION Anesthesia System.
Brand
Maquet Inc
Lot Codes / Batch Numbers
Serial Number: 2034, 3416, 3417, 3418, 3419, 3420, 3027, 0501, 3394, 3395, 3396, 3433, 3444, 3445, 3446, 2355, 2356, 2033, 2035, 1838, 1839, 1840, 1841, 1842, 1873, 1874, 1875, 1876, 1877, 1899, 1900, 1902, 1903, 2132, 2032, 1723, 1724, 1725, 1726, 1727.
Products Sold
Serial Number: 2034; 3416; 3417; 3418; 3419; 3420; 3027; 0501; 3394; 3395; 3396; 3433; 3444; 3445; 3446; 2355; 2356; 2033; 2035; 1838; 1839; 1840; 1841; 1842; 1873; 1874; 1875; 1876; 1877; 1899; 1900; 1902; 1903; 2132; 2032; 1723; 1724; 1725; 1726; 1727.
Maquet Inc is recalling KION Anesthesia System. due to Software update so US customers will be updated equally with worldwide customers. Ver. 5.0 will be upgraded to ver 7.0. Quality will improve and enh. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software update so US customers will be updated equally with worldwide customers. Ver. 5.0 will be upgraded to ver 7.0. Quality will improve and enhance functionality.
Recommended Action
Per FDA guidance
MCC has assigned an internal task team to manage plan and perform the correction ofthe installed base of KION (intended for clinical use) in US. Updates started on January 11, 2005.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026