Z-0159-04

UHF Grollman Pigtail Long Tip Non-wirebraid, 7FG, 110 cm, Angiographic Catheter, Sterile, Merit Medical

Name: Z-0159-04 UHF Grollman Pigtail Long Tip Non-wirebraid, 7FG, 110 cm, Angiographic Catheter, Sterile, Merit Medical
Creator: Merit Medical Systems, Inc
Published: 2003-11-05
License: https://open.fda.gov/license/

Merit Medical Systems, Inc. / initiated 2003-11-05 / Terminated

FDA source

Merit Medical Systems, Inc began a recall of UHF Grollman Pigtail Long Tip Non-wirebraid, 7FG, 110 cm, Angiographic Catheter, Sterile, Merit Medical on 2003-11-05. The reason FDA records is "Angiographic catheter tips may separate during use". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0159-04
Status: Terminated
Initiated: 2003-11-05
Posted: 2003-11-27
Terminated: 2003-12-01
Recalling firm: Merit Medical Systems, Inc.
Product: UHF Grollman Pigtail Long Tip Non-wirebraid, 7FG, 110 cm, Angiographic Catheter, Sterile, Merit Medical.
Product code: DQO Catheter, Intravascular, Diagnostic
Reason for recall: Angiographic catheter tips may separate during use.
FDA root cause: Other
Action: All 7 consignees were contacted by their sales representatives on 11/5-7/2003.
Quantity in commerce: 32 units
Distribution: FL, MI, NY, PA, TN, TX. No foreign, government, or military distribution.
Product codes and lots: Catalog Number 5614-A0, Lot G260778

Product code DQO

K943739Class IISoftouch Diagnostic Intravascular CatheterMallinckrodt Medical / cleared 1994-11-15

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)