FDAOctober 21, 2015device

LeMaitre Over-the-Wire Embolectomy Catheter 4F, 80cm, Model 1651-48 and e1654-48. Indicated for the removal of arterial emboli and thrombi.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.

What to do

FDA enforcement status: Terminated

Brands named

lemaitre vascularlemaitre

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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LeMaitre Over-the-Wire Embolectomy Catheter 4F, 80cm, Model 1651-48 and e1654-48. Indicated for the removal of arterial emboli and thrombi. — Recall Details · AllClear