Datex-Ohmeda Inc One Ohmeda Datex-Ohmeda Cardiocap/5 Patient Monitors Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Datex-Ohmeda Cardiocap/5 Patient Monitors
Brand
Datex-Ohmeda Inc One Ohmeda
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
The monitors in the serial number range FBWF00725 through FBWF03055 and FBWG00001 through FBWG02015 could be affected by the problem if they are mounted on the optional mounting stands for the product. The consignees notified of the field correction had purchased both the monitors and the stands.
Datex-Ohmeda Inc One Ohmeda is recalling Datex-Ohmeda Cardiocap/5 Patient Monitors due to Datex-Ohmeda Cardiocap/5 Patient Monitors have bracket pins which do not adequately secure them to their optional mounting stand so the monitors may f. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Datex-Ohmeda Cardiocap/5 Patient Monitors have bracket pins which do not adequately secure them to their optional mounting stand so the monitors may fall.
Recommended Action
Per FDA guidance
Recall letters dated October 15, 2003 were sent to the consignees on 10/17/03. The letters request that the consignees order service kits to correct the units and use the kits to make the corrections of the devices.
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