EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Reported: January 29, 2025 Initiated: December 12, 2024 #Z-0985-2025
Product Description
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Reason for Recall
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Details
- Recalling Firm
- Medtronic Perfusion Systems
- Units Affected
- 930 units
- Distribution
- Worldwide - US Nationwide distribution.
- Location
- Brooklyn Park, MN
Frequently Asked Questions
What product was recalled? ▼
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr). Recalled by Medtronic Perfusion Systems. Units affected: 930 units.
Why was this product recalled? ▼
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 29, 2025. Severity: Moderate. Recall number: Z-0985-2025.
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