Karl Storz Endoscopy 2022-05-18 Health serious FDA
Health · FDA · Recall #FDA-Z-1055-2022
11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) Recall
Issued May 18, 2022 · Karl Storz Endoscopy
In May 2022, Karl Storz Endoscopy recalled the 11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019), a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.
What you should do
- 1 Stop using 11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Karl Storz Endoscopy to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Karl Storz Endoscopy
- Category
- Health
- Recall date
- May 18, 2022
- Units affected
- Not reported
- Sold at
- U.S. Nationwide distribution in the states of FL, KY, LA, MA, MI, MO, MT, NC, NH, NJ, OK, SC, TX and WA.
- Recall number
- FDA-Z-1055-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Karl Storz Endoscopy has 8 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.