FDA Device recall Z-0001-2022
RAPTAR Laser Range Finders
- FDA Device
- Class II
- ongoing
- Published 2021-11-03
On 2021-11-03 the FDA classified a Class II recall of RAPTAR Laser Range Finders by Potomac River Group, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0001-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-04-21 |
| Published | 2021-11-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Potomac River Group |
| Distribution | US |
Product
RAPTAR Laser Range Finders
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.
Identifiers
| code_info | RAPTAR G02 (Wilcox Part #57200G02) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0001-2022%22
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