Class I
Medical Device Recall: Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C
MEDLINE INDUSTRIES, LP - Northfield · April 22, 2025
Reason for Recall
Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
Distribution
US distribution to CA, FL, IL, IN, KY, MA, MD, MN, NY, TX, VT, WA and WI. No OUS distribution.
States Affected
CA, FL, IL, IN, KY, MA, MD, MN, NY, TX, VT, WA, WI
Quantity Affected
1853 total
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1810-2025
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.