Z-0268-2014Class I

ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZRXT180S...

Name: Z-0268-2014 ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZRXT180S...
Creator: Medtronic Vascular
Published: 2013-10-21
License: https://open.fda.gov/license/

Medtronic, Inc. / initiated 2013-10-21 / Terminated / root cause: manufacturing process

FDA source

Medtronic Vascular began a recall of ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZRXT180S Medtronic guide wires are steerable guide wires that... on 2013-10-21. FDA classified it as Class I and gives the reason as "Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0268-2014
Classification: Class I
Status: Terminated
Initiated: 2013-10-21
Posted: 2013-11-15
Terminated: 2014-12-15
Recalling firm: Medtronic, Inc.
Product: ZINGER Steerable Guidewire; Models: LVZRLS180J, LVZRLS180S, LVZRMS180J, LVZRMS180S, LVZRXT180J, LVZRXT180S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral vasculature, and may be used to reach and cross a target lesion. Medtronic guide wires are not intended for cerebral vasculature. Medtronic steerable exchange guide wires are used to facilitate the substitution of one diagnostic or interventional device for another.
Product code: DQT Occluder, Catheter Tip
Reason for recall: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach from Guidewire.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: The firm, Medtronic, sent a "URGENT MEDICAL DEVICE RECALL" letter dated October 21, 2013 (in the US via UPS overnight service, 1-day delivery) to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to immediately remove and quarantine all potentially affected guidewires that remain in inventory; return the affected product to Medtronic; if replacement product is needed, your Medtronic representative can assist you with identifying suitable replacement product, and to complete and return the Customer Confirmation Certificate confirming receipt of the notification via fax to Medtronic at 651-367-0612 to the attention of Customer Focused Quality (100% customer confirmations will be required). Should have any questions, please contact your Medtronic Representative or call 763-526-2513. Notifications to customers concerning the additional affected product began December 19, 2013 (in the US via UPS overnight service, 1-day delivery). Customers are requested to return a Confirmation Certificate confirming their receipt of the notification. 100% customer confirmations will be required from the additional consignees.
Quantity in commerce: 5
Distribution: Worldwide distribution: US (Nationwide) including states of: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WV; and countries of: Albania, Algeria, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, Georgia, Germany, Greece, Guyana, Honduras, Hong Kong,Hungary, Iceland, India, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Libya, Luxembourg, Malaysia, Mexico, Montenegro, Nepal, Netherlands, New Zealand, Nepal, Nicaragua, Norway, Oman, Poland, Portugal Puerto Rico, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, United Kingdom, Uruguay, and Yemen.
Product codes and lots: G13A00118 G13A00715 G13A00716 G13A00843 G13A00937 G13A01601 G13A01620 G13A01621 G13A01638 G13A01639 G13A01650 GV854 GW761

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0268-2014
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0261-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0262-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0263-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0264-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0265-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0266-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0267-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15
Z-0268-2014	Class I	Terminated	Voluntary: Firm initiated	2013-11-27	2013-11-15

Product code DQT

K983927Class IIGt1 Floppy, Gt1 Hi-per Flex, Gt1 Light SupportArterial Vascular Engineering, Inc. / cleared 1999-03-11

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)