Z-1472-2024 Class II Ongoing
FDA device recall Z-1472-2024 was initiated by Karl Storz Endoscopy on Feb 27, 2024 and is designated Class II. Reason for recall: Inadequate reprocessing validation evidence The recall status is ongoing. Affected quantity: 190 units.
Recall Details
- Product Type
- Devices
- Report Date
- Apr 10, 2024
- Initiation Date
- Feb 27, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 190 units
Product Description
Karl Storz SE & CO. KG, REF 11003MB, Grasping Forceps, Flexible 1 mm, Rx Only
Reason for Recall
Inadequate reprocessing validation evidence
Distribution Pattern
US Nationwide distribution in the states of AR, CA, CO, CT, DC, FL, GA, IA, IL, LA, MA, MI, MN, MO , ND, NY, OH, OR, SD, TN, TX, UT, VA, WA, WV.
Code Information
UDI: 04048551050255/ All Lots
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1472-2024
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026