Z-1003-03

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

Name: Z-1003-03 ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100
Creator: Life-Tech International, Inc
Published: 2001-05-09
License: https://open.fda.gov/license/

Life-Tech International, Inc / initiated 2001-05-09 / Terminated

FDA source

Life-Tech International, Inc began a recall of ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100 on 2001-05-09. The reason FDA records is "Catheter does not fit through the needle resulting in delay of medical procedure". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1003-03
Status: Terminated
Initiated: 2001-05-09
Posted: 2003-07-15
Terminated: 2003-07-15
Recalling firm: Life-Tech International, Inc
Product: ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100
Product code: CAZ Anesthesia Conduction Kit
Reason for recall: Catheter does not fit through the needle resulting in delay of medical procedure
FDA root cause: Other
Action: The firm initiated the recall via letter to all consignees on May 9, 2001.
Distribution: CA, MN, TX, FL, UT,
Product codes and lots: All manufacturing codes were recalled. Model numbers: PL-50, PL-100

Product code CAZ

K001129Class IIProlong, Models Pl50, Pl100, Pl150Life-Tech Intl., Inc. / cleared 2000-07-06

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)