Recall Z-1465-2022— Zeiss, Carl Inc
Class III · Terminated
Class III FDA medical device recall by Zeiss, Carl Inc, initiated 2022-06-24, terminated 2025-02-07. FDA's recall record names no specific 510(k) clearance for this event. Product: ZEISS Axio Observer 5 microscope, Product material no. 431006-9901-000. Reason: An incorrect Unique Device Identification (UDI) label was installed on some ZEISS Axio Observer 5 microscopes..
- Recalling firm
- Zeiss, Carl Inc
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2022-06-24
- Terminated
- 2025-02-07
- Firm location
- Thornwood, NY, United States
Product description
ZEISS Axio Observer 5 microscope, Product material no. 431006-9901-000
Reason for recall
An incorrect Unique Device Identification (UDI) label was installed on some ZEISS Axio Observer 5 microscopes.
Data sourced from openFDA. This site is unofficial and independent of the FDA.