Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The connectors may not allow catheters to be...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MEDLINE INDUSTRIES, LP - Northfield directly.
Affected Products
MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZATION KIT, REF PAIN1644
Quantity: 3006 units
Why Was This Recalled?
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MEDLINE INDUSTRIES, LP - Northfield
MEDLINE INDUSTRIES, LP - Northfield has 822 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report