Z-0888-2007

Patrol enteral pump set with piercing pin, list #520540

Name: Z-0888-2007 Patrol enteral pump set with piercing pin, list #520540
Creator: Ross Products Division Abbott Laboratories
Published: 2007-05-02
License: https://open.fda.gov/license/

Ross Products Division Abbott Laboratories / initiated 2007-05-02 / Terminated

FDA source

Ross Products Division Abbott Laboratories began a recall of Patrol enteral pump set with piercing pin, list #520540 on 2007-05-02. The reason FDA records is "The enteral pump set may have a 1-3 mm slit in the silicone tubing located between the blue connector and the stretch band Safe-T-Valve". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0888-2007
Status: Terminated
Initiated: 2007-05-02
Posted: 2007-07-10
Terminated: 2012-03-09
Recalling firm: Ross Products Division Abbott Laboratories
Product: Patrol enteral pump set with piercing pin, list #520540.
Product code: KNT Tubes, Gastrointestinal (And Accessories)
Reason for recall: The enteral pump set may have a 1-3 mm slit in the silicone tubing located between the blue connector and the stretch band Safe-T-Valve.
FDA root cause: Other
Action: The recalling firm sent a recall letter dated April 27, 2007 to all customers.
Quantity in commerce: 1,042,050 units
Distribution: Nationwide
Product codes and lots: Lots 45679RY, 46740RY, 46759RY, 46776RY, 47799RY, 47814RY, 47825RY, 47832RY, 47842RY, 48854RY, and 48869RY.

Product code KNT

K943240Class IIFlexiflo Six Enteral Nutrition Pump SetAbbott Laboratories / cleared 1995-04-13

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)