Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
Reported: May 22, 2024 Initiated: March 19, 2024 #Z-1796-2024
Product Description
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001
Reason for Recall
Potential for unsealed sterile packing.
Details
- Recalling Firm
- Medtronic Perfusion Systems
- Units Affected
- 7935 units
- Distribution
- Worldwide distribution.
- Location
- Brooklyn Park, MN
Frequently Asked Questions
What product was recalled? ▼
Medtronic I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001. Recalled by Medtronic Perfusion Systems. Units affected: 7935 units.
Why was this product recalled? ▼
Potential for unsealed sterile packing.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 22, 2024. Severity: Moderate. Recall number: Z-1796-2024.
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