FDA Medical Device Recalls (openFDA)
Karl Storz Endovision, Inc.: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use, non-sterile device for cleaning various models of endoscopes Model Number: 11276CL
- Recall number
- Z-1333-2016
- Recalling firm
- Karl Storz Endovision, Inc.
- Product
- ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use, non-sterile device for cleaning various models of endoscopes Model Number: 11276CL
- Status
- Terminated
- Initiated
- 2016-02-29
- Posted
- not on file
- Terminated
- 2016-09-28
- 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.
- Root cause
- Component design/selection
- Action
- Karl Storz issued Recall Letter to users on 12/23/15. Firm's letter: KARL STORZ has identified a replacement brush; model 11276CL2 that is now available to clean your endoscope. Please check your inventory and remove any model 11276CL brushes. These brushes must be returned to KARL STORZ. Please complete the attached form and followthe return instructions. Upon receipt of any 11276CL brushes from you we will provide you the 11276CL2 cleaning brush as replacement at no charge. Contact Lynn Carter, Director Quality Assurance at 508-248-9011, extension 1664 Monday through Friday, 8:00AM to 4:30PM, Eastern Time.
- Quantity
- 16908 brushes
- Distribution
- Nationwide Foreign: Canada, Mexico,
- Lot, serial or model codes
- All lot numbers
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- MNL
- Firm FEI
- 1221826
- Firm city
- Charlton
- Firm state
- MA
- 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