Class II

Medical Device Recall: Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.

AVID Medical, Inc. · March 31, 2025

Reason for Recall

An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.

Distribution

US Nationwide distribution in the states of IL & LA.

States Affected

NATIONWIDE

Quantity Affected

72 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1743-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.