Z-1122-2022 Class II Terminated
FDA device recall Z-1122-2022 was initiated by Olympus Corporation Of The Americas on Mar 31, 2022 and is designated Class II. Reason for recall: Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps The recall status is terminated (terminated Jul 25, 2024). Affected quantity: 1386 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 1, 2022
- Initiation Date
- Mar 31, 2022
- Termination Date
- Jul 25, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1386 units
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
Distribution Pattern
US Nationwide Distribution
Code Information
Lot numbers since January 2017. Affected Lot Numbers: 01K 02K 03K 04K 05K 06K 07K 08K 09K 0XK 0YK 0ZK 11H 11K 12K 13K 14K 15K 16K 17K 18K 19K 1XK 71K 72K 73K 74K 75K 76K 77H 77K 78K 79K 7XK 7YK 7ZK 81K 82K 83K 84K 85K 86K 87K 88K 89K 8XK 8YK 8ZK 91K 92K 93K 94K 95K 96K 97K 98K 99K 9XK 9YK 9ZK
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1122-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026