Class II — Synergetics Inc
| Recalling firm | SYNERGETICS, INC. |
|---|---|
| Registered facility | SYNERGETICS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23 gauge cannulas; the product is labeled as 25 gauge cannulas. |
| Product | Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog number: 30.08.25. Single-use 25 gauge cannula used in vitreoretinal surgery. |
| Quantity | 48/6-cannula boxes |
| Distribution | Nationwide Distribution-USA including the states of MO, CO, KY, TN, NC, PA, IL CA, NY, IN, MI, LA, NJ and OH. |
| Initiated | 2013-07-30 |
| Classified | 2013-10-22 |
| Terminated | 2014-04-07 |
| Recall number | Z-0051-2014 |
| 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 — Synergetics Inc (Z-0051-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65969/
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