Medtronic Perfusion Systems Recall: DLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only
Medtronic Perfusion Systems Recall: DLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Medtronic Perfusion Systems; Product: DLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only; Reason for recall: Potential for a wire protrusion th
| Recalling firm | Medtronic Perfusion Systems |
|---|---|
| Product | DLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only |
| Reason for recall | Potential for a wire protrusion through the left heart vent catheter tip |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Nationwide distribution to AL, CA, CO, DC, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI. International distribution to Albania, Algeria, Australia, Austria, Azerbaijan, Bangladesh, Belgium, Botswana, Brazil, Bulgaria, Camb |
| Recall initiated | 20210824 |
| Recall number | Z-2505-2021 |
| Category | device |
| State | MN |
| Country | United States |
$29/mo
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