Z-0568-2023 Class II Ongoing
FDA device recall Z-0568-2023 was initiated by DeRoyal Industries Inc on Nov 3, 2022 and is designated Class II. Reason for recall: DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled. The recall status is ongoing. Affected quantity: 135 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Dec 21, 2022
- Initiation Date
- Nov 3, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 135 kits
Product Description
GEO-MED SHOULDER ARTHROSCOPY KNEE PACK, REF 89-5797.09
Reason for Recall
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
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: Lot 56392226 exp 9/1/2023; Lot 56683525 exp 9/1/2023; Lot 57001506 exp 4/1/2024
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0568-2023
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026