FDA Medical Device Recalls (openFDA)
Amstech Incorporated: Aimshot HeatSeeker Model HS3500, contains Class IIIb infared laser illuminator. Amstech Incorporated, Alpharetta, GA 30022. Targeting, detecting heated areas, searches.
- Recall number
- Z-0507-2011
- Recalling firm
- Amstech Incorporated
- Product
- Aimshot HeatSeeker Model HS3500, contains Class IIIb infared laser illuminator. Amstech Incorporated, Alpharetta, GA 30022. Targeting, detecting heated areas, searches.
- Status
- Terminated
- Initiated
- 2010-08-17
- Posted
- 2010-12-22
- Terminated
- 2011-11-09
- Reason
- Product contains infra red laser, which can pose a potential hazard to users who unknowingly shine the beam into people's eyes.
- Root cause
- Radiation Control for Health and Safety Act
- Action
- Firm sent a letter dated August 5, 2010 to customers stating that a recall was being conducted on the AimSHOT HeatSeeker and specified model. The letter stated the reason for the recall and that the firm has redesigned the HeatSeeker and removed the infra red laser feature. The letter also asks customers to check their inventory and return the affected products to the firm. The firm states that they will send customers their new model and pay for the shipping. Questions should be directed towards 770-840-8039.
- Quantity
- All units
- Distribution
- Nationwide Distribution
- Lot, serial or model codes
- Model HS3500
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- REP
- Firm FEI
- 3002828006
- Firm city
- Alpharetta
- Firm state
- GA
- 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