FDA Medical Device Recalls (openFDA)
Potomac River Group, Corp.: RAPTAR Laser Range Finders
- Recall number
- Z-0001-2022
- Recalling firm
- Potomac River Group, Corp.
- Product
- RAPTAR Laser Range Finders
- Status
- Open, Classified
- Initiated
- 2021-04-21
- Posted
- not on file
- Terminated
- not on file
- Reason
- RAPTAR units are capable of being field modified to enable the use of the higher power visible and IR laser pointers and the IR Illuminator.
- Root cause
- Radiation Control for Health and Safety Act
- Action
- Potomac River Group (PRG) sent communications to the purchasers of the affected units that were locked in the eye safe mode and distributed without the keys. PRG expects to offer all affected purchasers at least a refund option. PRG s ability to offer a repair option is contingent upon assistance from Wilcox, which is the only entity PRG is aware of that has the ability to render the units compliant with FDA specifications.
- Quantity
- 62 units
- Distribution
- US Nationwide
- Lot, serial or model codes
- RAPTAR G02 (Wilcox Part #57200G02)
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- REP
- Firm FEI
- 3004918946
- Firm city
- Ashburn
- Firm state
- VA
- 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