Drug recall
Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used…
FDA recall event 79669 · Class II · Crimson Trace Corporation
Key facts
| Event ID | 79669 |
|---|---|
| Recall numbers | Z-1361-2018 |
| Recalling firm | Crimson Trace Corporation |
| Product type | Devices |
| Products | Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used for personal defense and target acquisition. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA Requested |
| Reason for recall | A previously "in specification" Finished Product with a Model 25-0657 diode had power output higher than 5 mW. |
| Initiation date | Oct 10, 2017 |
| Report date | May 2, 2018 |
| Termination date | Nov 22, 2019 |
| City | Wilsonville |
| State | OR |
| Country | United States |
| FEI number | 3006733130 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: