Z-0713-2023 Class II Ongoing
FDA device recall Z-0713-2023 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: 552 units.
Recall Details
- Product Type
- Devices
- Report Date
- Dec 21, 2022
- Initiation Date
- Nov 3, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 552 units
Product Description
DeRoyal CATARACT PACK, REF 89-9241.04
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: 57198898 exp 12/01/2024; 57686605 exp 04/01/2025; 57754049 exp
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0713-2023
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026