MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
- Recall date
- October 16, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0514-2025
- 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.
What was recalled
MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
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