[Recalled] LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus, 80cm, Model 1651-88 and e1654-88. Indicated for the removal of arterial emboli and thrombi. — Manufacturing issue that could cause a pinhole in the formed end of the packagi…
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus, 80cm, Model 1651-88 and e1654-88. Indicated for the removal of arterial emboli and thrombi. |
|---|---|
| Brand / manufacturer | LeMaitre Vascular, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0381-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 21 October 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from LeMaitre Vascular, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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