FDA Medical Device Recalls (openFDA)
Mentor Texas, Inc: 5mm x 30cm Hollow "Golf" Tip Ultrasonic Aspiration Probe, Model 5620-530, Catalog Number 5620-530.
- Recall number
- Z-1230-2007
- Recalling firm
- Mentor Texas, Inc
- Product
- 5mm x 30cm Hollow "Golf" Tip Ultrasonic Aspiration Probe, Model 5620-530, Catalog Number 5620-530.
- Status
- Terminated
- Initiated
- 2007-07-27
- Posted
- 2007-09-20
- Terminated
- 2008-04-04
- Reason
- Mis-identified and mis-labeled surgical probes were distributed. 5mm x 30cm Hollow "Golf" Tip Ultrasonic Aspiration Probe, Model 5620-530, Catalog Number 5620-530 was shipped, instead of LySonix 5mm x 30cm Hollow Bullet Tip Ultrasonic Probe, Catalog Number 5610-530.
- Root cause
- Other
- Action
- Firm notified consignees by letter on July 27, 2007.
- Quantity
- 4 units
- Distribution
- Nationwide, including VA, IN, CA, and IL.
- Lot, serial or model codes
- Serial numbers: 0028-05, 0035-05, 0069-05, and 0092-05
- 510(k) numbers
- ["K041058"]
- PMA numbers
- not on file
- Product code
- MUU
- Firm FEI
- 1000118360
- Firm city
- Irving
- Firm state
- TX
- 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