Class II — Med-logics Inc
| Recalling firm | MED-LOGICS, INC. |
|---|---|
| Registered facility | MED-LOGICS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The ML 7090 Calibrated LASIK Blade (CLB) will not fit into the AMO Amadeus Metal Blade Holder. |
| Product | ML 7090 Calibrated LASIK Blade (CLB); CLB CALIBRATED LASIK BLADE 10. ML 7090 Calibrated LASIK Blade (CLB) is to be used as replacement blades for the AMO Amadeus Microkeratome, to perform lamellar keratectomy procedures. |
| Quantity | 360 units |
| Distribution | Distributed in the states of CA, AL, GA, and TN, and the countries of Chile and Germany. |
| Initiated | 2015-01-13 |
| Classified | 2015-03-13 |
| Terminated | 2015-10-28 |
| Recall number | Z-1268-2015 |
| 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 — Med-logics Inc (Z-1268-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70348/
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