DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Reported: January 29, 2025 Initiated: December 12, 2024 #Z-0984-2025
Product Description
DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Reason for Recall
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Details
- Recalling Firm
- Medtronic Perfusion Systems
- Units Affected
- 745 units
- Distribution
- Worldwide - US Nationwide distribution.
- Location
- Brooklyn Park, MN
Frequently Asked Questions
What product was recalled? ▼
DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr). Recalled by Medtronic Perfusion Systems. Units affected: 745 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-0984-2025.
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