FDA Medical Device Recalls (openFDA)
Covidien LLC: Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems. Product Number/CFN: 186-0208 UDI-Device Identifier (GTIN/UPN): 10884521130319
- Recall number
- Z-2958-2018
- Recalling firm
- Covidien LLC
- Product
- Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems. Product Number/CFN: 186-0208 UDI-Device Identifier (GTIN/UPN): 10884521130319
- Status
- Open, Classified
- Initiated
- 2018-07-26
- Posted
- not on file
- Terminated
- not on file
- Reason
- Revised replacement instructions for the Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems
- Root cause
- Device Design
- Action
- Medtronic U.S. consignees were notified via Federal Express or certified mail on July 26, 2018, and the letter informs customers to inspect their batteries. Batteries with date code 3114 or older (Week 31 of 2014) exceed 4 years of age and should be removed from the monitor and disposed of according to facilitys standard process. Included with this notification are stickers to be placed on BIS" monitors when the battery pack is removed the stickers No Battery Installed should be placed on the monitors. The BIS Vista and View monitoring systems may be used without a battery pack only if connected to AC power source with emergency power backup system (Red Outlet).
- Quantity
- BIS 46,961; Spare Batteries: 6,937
- Distribution
- Nationwide Foreign: Australia, New Zealand
- Lot, serial or model codes
- Batteries with date code 3114 or older (Week 31 of 2014)
- 510(k) numbers
- ["K072286"]
- PMA numbers
- not on file
- Product code
- OLW
- Firm FEI
- 1219930
- Firm city
- North Haven
- Firm state
- CT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28