FDA Device recall Z-0514-2025
MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
- FDA Device
- Class II
- ongoing
- Published 2024-12-04
On 2024-12-04 the FDA classified a Class II recall of MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A by Medline Industries Northfield, citing the connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0514-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-10-16 |
| Published | 2024-12-04 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
Reason
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Identifiers
| code_info | Codes: 1) PAIN1876A UDI-DI: 10195327433666 (each) 40195327433667 (case), Lot Number: 23KLA330 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0514-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.