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Terminated

ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100

FDA Recall Z-1003-03 · Posted 2003-07-15

Recalling FirmLife-Tech International, Inc
Recall StatusTerminated
Product CodeCAZ
Date Initiated2001-05-09
Date Terminated2003-07-15

Reason for Recall

Catheter does not fit through the needle resulting in delay of medical procedure

Firm Action

The firm initiated the recall via letter to all consignees on May 9, 2001.

Root Cause

Other

Distribution Pattern

CA, MN, TX, FL, UT,

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K001129PROLONG, MODELS PL50, PL100, PL150Life-Tech Intl., Inc. · 2000-07-06

Official Source

View FDA Recall →

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

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