Z-2366-2023 Class II Ongoing
FDA device recall Z-2366-2023 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Jul 3, 2023 and is designated Class II. Reason for recall: The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit. The recall status is ongoing. Affected quantity: 16 kits.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 16, 2023
- Initiation Date
- Jul 3, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 16 kits
Product Description
Total Hip Kit, REF DYNJ903275S; surgical convenience kit
Reason for Recall
The prep solution included in the Total Hip Kit expires prior to the expiration date of the Kit.
Distribution Pattern
US Nationwide distribution in the state of Illinois.
Code Information
UDI/DI: 10195327254582 (unit), 40195327254583 (case); Lot code 23CDC733
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2366-2023
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026