Z-1017-2015Class I

Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and...

Name: Z-1017-2015 Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and...
Creator: Covidien
Published: 2014-12-10
License: https://open.fda.gov/license/

Medtronic, Inc. / initiated 2014-12-10 / Terminated / root cause: labeling and UDI

FDA source

Covidien began a recall of Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for... on 2014-12-10. FDA classified it as Class I and gives the reason as "A manufacturing error resulted in the risk of incorrect proximal and distal balloon inflation port identification on the units. Units have been identified to have the distal balloon inflation port incorrectly labeled as...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-1017-2015
Classification: Class I
Status: Terminated
Initiated: 2014-12-10
Posted: 2015-02-03
Terminated: 2016-03-31
Recalling firm: Medtronic, Inc.
Product: Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.
Product code: KRA Catheter, Continuous Flush
Reason for recall: A manufacturing error resulted in the risk of incorrect proximal and distal balloon inflation port identification on the units. Units have been identified to have the distal balloon inflation port incorrectly labeled as proximal, and, the proximal balloon port incorrectly labeled as distal.
Root cause tag: labeling and UDI
FDA root cause: Mixed-up of materials/components
Action: Consignees were sent an Urgent Product Recall letter dated 12/15/2014. The letter described the issue, identified the affected product, and the required actions. Affected product was to be returned directly to customers' Covidien Sales Rep; or customers were to contact Covidien Service at 1-800-716-6700 to arrange for product return. Questions can be directed to the Covidien Sales Rep or to Covidien Service at 1-800-716-6700. Customers were to complete and return the Verification Form along with the unused product as soon as possible.
Quantity in commerce: 216 devices (207 US, 9 OUS)
Distribution: Worldwide Distribution - US Nationwide and the countries Australia, Canada, Finland, France, Germany, Ireland, Italy, Spain, Sweden, Switzerland, Turkey, and United Kingdom.
Product codes and lots: Model BVT608010, Lot numbers: 9853174, 9864497, 9890772, 9890931, 9925676, 9932672, 9937308, 9937315, 9940474, 9940614, 9976340, 9978233, A001589, A001740. Model BVT608030, Lot Numbers: 9853331, 9887597, 9887695, 9887757, 9932042. Model BVT612010, Lot numbers: 9854121, 9868214, 9868311, 9875472, 9875632, 9876174, 9883295, 9884788, 9884951, 9886196, 9886312, 9932096, 9968511, 9974109, 9974126, 9976472, 9977091, 9978862, A002299, A002423. Model BVT312030, Lot numbers: 9854124, 9892081, 9941213, 9971096, 9971139, 9976506, 9977140, 9978964, 9979548, A003021, A003121, A003651, A007900, A008492, A008603, A008687.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1017-2015
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1017-2015	Class I	Terminated	Voluntary: Firm initiated	2015-02-11	2015-02-02
Z-1018-2015	Class I	Terminated	Voluntary: Firm initiated	2015-02-11	2015-02-02

Product code KRA

K071664Class IITrellis-6 Peripheral Infusion SystemBacchus Vascular, Inc. / cleared 2007-07-13

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 2026-10-14, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)