FDA Medical Device Recalls (openFDA)
Medtronic Neuromodulation: SenSight Connector Plug, Model Number B31061.
- Recall number
- Z-0121-2024
- Recalling firm
- Medtronic Neuromodulation
- Product
- SenSight Connector Plug, Model Number B31061.
- Status
- Open, Classified
- Initiated
- 2023-01-20
- Posted
- 2023-10-18
- Terminated
- not on file
- Reason
- Medtronic is requesting return of a small number of units of the SenSight Connector Plug, Model B31061, due to a discrepancy in the Use By Date (UBD) printed on the label.
- Root cause
- Labeling Change Control
- Action
- Medtronic issued a MEDICAL DEVICE REMOVAL notice to its consignees on 01/20/2023 by mail. Consignees were asked to return any affected product they may have, and to forward this notification to those who need to be aware within the organization or to any location which the devices have been transferred.
- Quantity
- 65 devices
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- GTIN 00763000426576, Lot Number 082U30721
- 510(k) numbers
- not on file
- PMA numbers
- ["P960009S391"]
- Product code
- MHY
- Firm FEI
- 2182207
- Firm city
- Minneapolis
- Firm state
- MN
- 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