FDA recall Z-0838-2020

Imactis · Class II · device

Product

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,

Reason for recall

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

US: WI & IL

Key facts

Status
Ongoing
Initiation date
2019-08-01
Report date
2020-01-29
Voluntary/Mandated
Voluntary: Firm initiated
Location
St Martin D Heres, France

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0838-2020