Class II — Laser Peripherals LLC
| Recalling firm | LASER PERIPHERALS LLC. |
|---|---|
| Registered facility | LASER PERIPHERALS LLC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling that indicated a sterility expiration date as '2016-16' as opposed to the intended date of '2016-06'. |
| Product | LP,Surgical Fibers, Bare Laser Fiber 600 micron, DBLF-60-2, Sterile EO. Laser surgical instrument for use in general and plastic surgery and in dermatology |
| Quantity | 25 |
| Distribution | Nationwide Distribution to IL, IN, and MD |
| Initiated | 2014-06-20 |
| Classified | 2014-07-17 |
| Terminated | 2014-10-22 |
| Recall number | Z-2073-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Laser Peripherals LLC (Z-2073-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68674/
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