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
Reported: December 4, 2024 Initiated: October 16, 2024 #Z-0512-2025
Product Description
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
Reason for Recall
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Details
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Units Affected
- 3006 units
- Distribution
- US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 3006 units.
Why was this product recalled? ▼
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 4, 2024. Severity: Moderate. Recall number: Z-0512-2025.
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