FDA Medical Device Recalls (openFDA)
Medtronic Neurosurgery: MurphyScope, Bayonet, Malleable, Catalog # 2121-157
- Recall number
- Z-0615-05
- Recalling firm
- Medtronic Neurosurgery
- Product
- MurphyScope, Bayonet, Malleable, Catalog # 2121-157
- Status
- Terminated
- Initiated
- 2005-02-28
- Posted
- 2005-03-12
- Terminated
- 2005-07-12
- Reason
- Products are mislabeled.
- Root cause
- Process control
- Action
- Recall letters were sent to customers on 2/28/05 requesting return for replacement.
- Quantity
- 2
- Distribution
- NJ and India.
- Lot, serial or model codes
- Lot A52300
- 510(k) numbers
- ["K010341"]
- 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