Recall Z-1122-2022— Olympus Corporation of the Americas
Class II · Terminated
Class II FDA medical device recall by Olympus Corporation of the Americas, initiated 2022-03-31, terminated 2024-07-25. FDA's recall record names no specific 510(k) clearance for this event. Product: Olympus DISPOSABLE GRASPING FORCEPS, FG-51D. Reason: Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps.
- Recalling firm
- Olympus Corporation of the Americas
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2022-03-31
- Terminated
- 2024-07-25
- Firm location
- Center Valley, PA, United States
Product description
Olympus DISPOSABLE GRASPING FORCEPS, FG-51D
Reason for recall
Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps
Data sourced from openFDA. This site is unofficial and independent of the FDA.