Karl Storz Endoscopy 2025-02-05 Health serious FDA
Health · FDA · Recall #FDA-Z-1052-2025
KARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE Recall
Issued February 5, 2025 · Karl Storz Endoscopy
In February 2025, Karl Storz Endoscopy recalled the KARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
What you should do
- 1 Stop using KARL STORZ - ENDOSKOPE, REF: 27030KA, Cysto-Urethroscope, NON STERILE, CE 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
- February 5, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-1052-2025
- 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 691st Health recall we've logged in 2025.