Z-0714-2023 Class II Ongoing
FDA device recall Z-0714-2023 was initiated by DeRoyal Industries Inc on Nov 3, 2022 and is designated Class II. Reason for recall: XXX The recall status is ongoing. Affected quantity: 108 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Dec 21, 2022
- Initiation Date
- Nov 3, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 108 kits
Product Description
DeRoyal CATARACT PACK, REF 89-10040.01
Reason for Recall
XXX
Distribution Pattern
US: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi
Code Information
Lot Numbers: 56125881 exp 05/01/2026; 56618926 exp 05/01/2026; 57485029 exp 11/01/2026
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0714-2023
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026