FDAFDA · Food and drugs·Recall number Z-3333-2026
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.
Published October 7, 2026 · Recall initiated: August 12, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Due to incorrect inside packaging label for eyepiece.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Karl Storz Endoscopy
- Distributor
- U.S. Nationwide distribution in the states of AZ, CA and MO.
- Lot
- Material Number: 10005BA UDI-DI code: 04048551045121 Serial Numbers: 100011, 100012, 10000Y, and 10000Z
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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Questions about this recall
Was 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. recalled?
Yes. FDA published recall Z-3333-2026 on October 7, 2026. Reported hazard: Due to incorrect inside packaging label for eyepiece.
What should I do if I have this product?
Voluntary: Firm initiated · Letter
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