FDA recall record

Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP recall — FDA Z-0917-2018

An EEPROM chip error code may occur when the catheters are used with CARTO EP Navigation Systems.

Class IIclassification
Z-0917-2018official record ID
Mar 14, 2018report date

Recall record at a glance

Official recordZ-0917-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStryker Sustainability Solutions
Report dateMar 14, 2018
Recall initiation dateJan 2, 2018
Quantity8 devices
LocationTempe, AZ, United States

Official product description

Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters, Ref D134302, Sterile, Rx. The Reprocessed 2515 NAV eco Variable Electrophysiology (EP) Catheters are indicated for multiple electrode electrophysiological mapping of the cardiac structures of the heart, i.e. recording or stimulation only. They are designed to obtain electrograms in the atrial regions of the heart. The Reprocessed 2515 NAV eco Variable EP Catheters provide location information when used with compatible CARTO EP Navigation Systems version 2.3 or higher.

Why the product was recalled

An EEPROM chip error code may occur when the catheters are used with CARTO EP Navigation Systems.

Distribution information

USA (nationwide) Distribution was made to medical facilities in AZ, CA, CT, FL, GA, IL, KS, LA, MN, MO, OH, PA, TX, VT, WA, and Wi. Foreign distribution was made to Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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