FDA recall record

Merit Laureate Hydrophilic Guide Wire, Catalog No recall — FDA Z-1485-2014

Discrepancy between the carton and unit labeling for the Merit Laureate Hydrophilic 0.035" 260 cm Guide Wire, catalog number LWSTFS35260EX, which has a…

Class IIclassification
Z-1485-2014official record ID
Apr 30, 2014report date

Recall record at a glance

Official recordZ-1485-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMerit Medical Systems, Inc.
Report dateApr 30, 2014
Recall initiation dateApr 14, 2014
Quantity173
LocationSouth Jordan, UT, United States

Official product description

Merit Laureate Hydrophilic Guide Wire, Catalog No. LWSTFS35260EX, Straight Tip Stiff Shaft, 0.035" (0.89mm), 260 cm (102").

Why the product was recalled

Discrepancy between the carton and unit labeling for the Merit Laureate Hydrophilic 0.035" 260 cm Guide Wire, catalog number LWSTFS35260EX, which has a straight tip and a stiff shaft. This lot was partially mixed with another lot of Laureate 0.035" 260 cm Guide Wire, catalog number LWSTDA35260EX, which has an angled tip, standard shaft and Chinese unit labeling.

Distribution information

Worldwide Distribution: USA Nationwide and China. No military/govt/VA consignees.

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: Letter.

What to do next

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