FDA recall record

Imactis Navigation Kit, REF 10100, Content Sterile Needle Holder Ref recall — FDA Z-0838-2020

The firm has become aware that the sensor cover, a component of the single-use navigation kit may contain microbial contamination. A source of microbial…

Class IIclassification
Z-0838-2020official record ID
Jan 29, 2020report date

Recall record at a glance

Official recordZ-0838-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmImactis
Report dateJan 29, 2020
Recall initiation dateAug 1, 2019
Quantity122 kits
LocationSt Martin D Heres, France

Official product description

Imactis Navigation Kit, REF 10100, Content Sterile Needle Holder Ref. A10010 CE 0459, Sensor Cover Ref. PC3688 CE 0482, Adhesif Film Ref. 38.20.15 CE 0459, EN Navigation Kit. Compatible with linear instruments of diameter ranging from 0.5 mm to 3.0 mm (25G to 11G), Sterile, Rx Only,

Why the product was recalled

The firm has become aware that the sensor cover, a component of the single-use navigation kit may contain microbial contamination. A source of microbial contamination has been identified in a raw product used to manufacture the tip of the cover.This could result in direct exposure of the intra-cardiovascular, intra-lymphatic or neurological system to a level of endotoxin sufficient to produce a pyrogenic response.

Distribution information

US: WI & IL

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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About this record

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