Recall Z-0837-2025— Karl Storz Endoscopy
Class II · Ongoing
Class II FDA medical device recall by Karl Storz Endoscopy, initiated 2024-12-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE. Reason: Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance..
- Recalling firm
- Karl Storz Endoscopy
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-12-19
- Firm location
- El Segundo, CA, United States
Product description
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Reason for recall
Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.
Data sourced from openFDA. This site is unofficial and independent of the FDA.