FDA Medical Device Recalls (openFDA)
Medtronic Neurosurgery: Channel Neuroendoscope, Standard Resolution, 21.6 cm. Catalog No. 2232-001
- Recall number
- Z-0049-04
- Recalling firm
- Medtronic Neurosurgery
- Product
- Channel Neuroendoscope, Standard Resolution, 21.6 cm. Catalog No. 2232-001
- Status
- Terminated
- Initiated
- 2003-09-15
- Posted
- 2004-07-20
- Terminated
- 2003-10-21
- Reason
- Size mix-up. 13 cm product may be labeled as 21.6 mm and visaversa.
- Root cause
- Labeling mix-ups
- Action
- Firm sales representatives will contact customers and hand deliver the recall notice.
- Quantity
- 10
- Distribution
- TN, CO, GA and Japan
- Lot, serial or model codes
- A20284
- 510(k) numbers
- ["K945633"]
- PMA numbers
- not on file
- Product code
- GWG
- Firm FEI
- 3015531529
- Firm city
- Goleta
- Firm state
- CA
- 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