FDAFDA · Food and drugs·Recall number Z-1095-2016
Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
Published March 23, 2016 · Recall initiated: December 23, 2015
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The sterile battery may contain particulates within the sterile package.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Pro-Dex Inc
- Distributor
- Distributed in FL.
- Lot
- Lots 509567, K055R
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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