Class II
Medical Device Recall: Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
Intrinsic Therapeutics, Inc. · July 25, 2024
Reason for Recall
At least two units have been found to be missing a weld.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
207 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2688-2024
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.