FDA Medical Device Recalls (openFDA)
Peregrine Surgical Ltd: Peregrine 20 GA Endo Ocular Adjustable Laser Probe
- Recall number
- Z-2399-2010
- Recalling firm
- Peregrine Surgical Ltd
- Product
- Peregrine 20 GA Endo Ocular Adjustable Laser Probe
- Status
- Terminated
- Initiated
- 2010-07-19
- Posted
- 2010-09-11
- Terminated
- 2010-09-30
- Reason
- Product did not have proper 510(k) clearance
- Root cause
- Other
- Action
- A recall letter is being sent to all affected accounts with instructions to return the recalled product to the recalling firm.
- Quantity
- 132 boxes
- Distribution
- Product was distributed to hospitals and eye surgery centers in Florida, Maryland, Missouri, North Carolina, Ohio, Pennsylvania, Texas.
- Lot, serial or model codes
- Device numbers: PD720.50, PD720.52, PD723.50, PD723.52, PD725.50, PD725.52. Lot numbers 926287, 937391, 931335, 933355, 935370, 937390, 940422, 916188, 917184, 919211, 920228, 922244, 925269, 916189, 917185, 919216, 920229, 923245, 925272, 952026, 002048, 005069, 916186, 918196, 919205, 920240, 924268, 926285, 916184, 918203, 919208, and 922239.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HQF
- Firm FEI
- 1000121498
- Firm city
- New Britain
- Firm state
- PA
- 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