Karl Storz Endoscopy recalls HOPKINS Telescope 30¿
- Recalling company
- Karl Storz Endoscopy
- Product
- HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.
- Reason
- Due to incorrect inside packaging label for eyepiece.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 12, 2026
- Reported
- Oct 7, 2026
- Distribution
- U.S. Nationwide distribution in the states of AZ, CA and MO.
- Status
- Ongoing
- Quantity
- 6 eyepieces
- Lot / codes
- Material Number: 10005BA UDI-DI code: 04048551045121 Serial Numbers: 100011, 100012, 10000Y, and 10000Z
- Company location
- El Segundo, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3333-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3333-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.