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Terminated

LeMaitre Embolectomy Catheter 4F Single Lumen, Balloon Volume 0.75 ml, Length 80 cm, Latex Model: 1601-48

FDA Recall Z-0559-05 · Posted 2005-02-24

Recalling FirmLemaitre Vascular, Inc.
Recall StatusTerminated
Product CodeDXE
Date Initiated2005-02-07
Date Terminated2005-07-25
Product Quantity411 units

Reason for Recall

Product sterility maybe compromised due to defective packaging

Firm Action

LaMaitre notified consignees by lettter advising users to check inventory and return defective product.

Root Cause

Other

Distribution Pattern

AL, CA, FL, IN, MD, MI,NY, TN, FOREIGN: Germany

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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