Z-0001-2022 Class II Ongoing
FDA device recall Z-0001-2022 was initiated by Potomac River Group, Corp. on April 21, 2021 and is designated Class II. Reason for recall: 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. The recall status is ongoing. Affected quantity: 62 units.
Recall Details
- Product Type
- Devices
- Report Date
- November 3, 2021
- Initiation Date
- April 21, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 62 units
Product Description
RAPTAR Laser Range Finders
Reason for Recall
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.
Distribution Pattern
US Nationwide
Code Information
RAPTAR G02 (Wilcox Part #57200G02)