Z-0350-2025 Class II Ongoing
FDA device recall Z-0350-2025 was initiated by MEDLINE INDUSTRIES, LP - Northfield on October 4, 2024 and is designated Class II. Reason for recall: Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap. The recall status is ongoing. Affected quantity: 80 units.
Recall Details
- Product Type
- Devices
- Report Date
- November 20, 2024
- Initiation Date
- October 4, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 80 units
Product Description
ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C
Reason for Recall
Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
Distribution Pattern
US Nationwide distribution in the state of TN.
Code Information
UDI-DI: 10195327246747; Lot Numbers: 24GBI464 24HBO800