FDA Medical Device Recalls (openFDA)
A.R.C. Laser Corp: A.R.C. Laser Photolysis Probe/Handpiece
- Recall number
- Z-0981-03
- Recalling firm
- A.R.C. Laser Corp
- Product
- A.R.C. Laser Photolysis Probe/Handpiece
- Status
- Terminated
- Initiated
- 2003-06-06
- Posted
- 2003-07-03
- Terminated
- 2003-07-23
- Reason
- Product may not have been properly sterilized.
- Root cause
- Other
- Action
- The 5 consignees were notified by phone on 06/06/2003, followed by fax and letter notification on 06/10/2003.
- Quantity
- 370 units
- Distribution
- IN, NY, PA, TX.
- Lot, serial or model codes
- Part Number: 1A55LM02 Catalog Number: LY11002
- 510(k) numbers
- ["K993154"]
- PMA numbers
- not on file
- Product code
- GEX
- Firm FEI
- 3003111512
- Firm city
- Salt Lake City
- Firm state
- UT
- 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