MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TR…

Recall date: October 16, 2024
Source: U.S. Food & Drug Administration (FDA) — enforcement report
Recall number: Z-0515-2025
FDA classification: Class II
Brand / firm: MEDLINE INDUSTRIES, LP - Northfield
Sold / distributed: US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands

Why it was recalled

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699A

Free email alert whenever MEDLINE INDUSTRIES, LP - Northfield has a new recall — straight from official government data. Unsubscribe anytime.