CLASS II ONGOING Device recall · Reported 3 Nov 2021 · FDA Enforcement Report
Raptar Laser Range Finders recalled by Potomac River Group
Potomac River Group is recalling Raptar Laser Range Finders, distributed nationwide in the US. The recall was initiated on 21 Apr 2021 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0001-2022
- FDA event ID
- 88735
- Recalling firm
- Potomac River Group, Ashburn, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 21 Apr 2021
- FDA classified
- 22 Oct 2021
- Reported
- 3 Nov 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 21 Apr 2021 | Recall initiated by company | |
| 22 Oct 2021 | Classified by FDA | +184 days |
| 3 Nov 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
RAPTAR Laser Range Finders
Where it was distributed
US Nationwide
Questions about this recall
Is Raptar Laser Range Finders recalled?
Yes. Potomac River Group recalled Raptar Laser Range Finders on 21 Apr 2021. The recall is Class II and its status is Ongoing. Recall number Z-0001-2022.
Why was it recalled?
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.
Which lots are affected?
RAPTAR G02 (Wilcox Part #57200G02)
Where was it sold?
US Nationwide
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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