Class II — Karl Storz Endovision, Inc.
| Recalling firm | KARL STORZ SE & CO KG |
|---|---|
| Registered facility | View this company's 11 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Endoscope cleaning brush 11276CL may not fit resulting in an inability to insert the brush in to the channel of the intended endoscope or to completely pass it through such channel. |
| Product | ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use, non-sterile device for cleaning various models of endoscopes Model Number: 11276CL |
| Quantity | 16908 brushes |
| Distribution | Nationwide Foreign: Canada, Mexico, |
| Initiated | 2016-02-29 |
| Classified | 2016-04-05 |
| Terminated | 2016-09-28 |
| Recall number | Z-1333-2016 |
| 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 — Karl Storz Endovision, Inc. (Z-1333-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72921/
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