Class II
Medical Device Recall: KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver 2.0 surgical driver, REF: KLS-SD-2000
Pro-Dex Inc · September 23, 2024
Reason for Recall
The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package.
Distribution
US distribution to FL only.
States Affected
FL
Quantity Affected
2000
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0280-2025
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.