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Health Canada Medical devices

MOLLI 2 Systems

Issued January 23, 2026
Issue
Stryker has updated the MOLLI 2 system Instructions for Use (IFU) following two medical device reports (MDRs) submitted to the FDA (June 5 2025). These reports involved patient injuries associated with MOLLI Marker dislodgement or dislocation due to magnetic attraction from magnetized surgical tools. The updated IFU now includes an additional warning that using magnetized surgical tools in close proximity to the marker during localization may lead to marker dislodgement.
Hazard description
Labelling and packaging
Product
Product name
MOLLI 2 Systems
Reference
ID
RA-81524