Abbott Recall 96545
Description: Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080
Abbott Recall 96545 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1643-2025 |
| Event ID | 96545 |
| Event Description | Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080 |
| Product Type | Devices |
| Distribution | Worldwide - US Nationwide distribution. |
| Quantity | 7,810 |
| Recall Reason | Device may have a small breach in the proximal end of the shaft under the strain relief of the delivery system. Breach is not visibly detectable and may lead to prolonged procedure, blood loss, or air ingress with potential for air embolism. |
| Device Classification | 20250430 |
| Device Code Info | Models: 1. 9-TVLP4F90/060; UDI-DI 00811806011561 Lots 9114256 9125090 9157327 9211450 10005333 10080103 10092488 10092519 10212158 10248201 10265245 10333989 10334851 10353324 2. 9-TVLP4F90/080; UDI-DI 00811806011578 Lots 9206150 10040010 10068340 10227816 10341801 |
| Center Classification Date | 20250421 |
| Recall Initiation Date | 20250317 |
| Recalling Firm | Abbott |
| Initial Notification | Letter |
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