Class II

Medical Device Recall: Halyard, Pain Pack. Kit Code: AMPK48-01.

AVID Medical, Inc. · April 30, 2026

Reason for Recall

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Distribution

US Nationwide distribution in the state of Iowa.

States Affected

NATIONWIDE

Quantity Affected

120 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2407-2026

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.

AVID Medical, Inc. Medical Device Recall: Halyard, Pain Pack. Kit Code: AMPK48-01. | SafeCheck