MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A
Reported: December 4, 2024 Initiated: October 16, 2024 #Z-0511-2025
Product Description
MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A
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
- 3396 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) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 3396 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-0511-2025.
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