Nihon Kohden America Inc AG-920RA Multi-gas unit analyzer Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AG-920RA Multi-gas unit analyzer
Brand
Nihon Kohden America Inc
Lot Codes / Batch Numbers
Serial numbers 00001 to 00020, 00022, 00023, 00024, 00029.
Products Sold
Serial numbers 00001 to 00020, 00022, 00023, 00024, 00029.
Nihon Kohden America Inc is recalling AG-920RA Multi-gas unit analyzer due to Manufacturing error results in screw affecting electromagnetic interferences. Also metal lid is not tight enough.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Manufacturing error results in screw affecting electromagnetic interferences. Also metal lid is not tight enough.
Recommended Action
Per FDA guidance
Consignees were notified on 12/5/03. All have received return authorizations.
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 noticeDistribution
As reported by FDA
CA, NV, OK
Page updated: Jan 10, 2026