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Pro-Dex Inc
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Pro-Dex Inc and translate it into plain English — free weekly digest, optional same-day alerts.
- 2024-11-06FDA-DeviceClass IIKLS 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
The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package.
- 2023-07-12FDA-DeviceClass IIKLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachment have switched manufacturing and expiration dates on sterile pouch labels, so batteries will appear to be prematurely expired.
- 2023-04-26FDA-DeviceClass IIKLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.
Incorrect Unique Device Identifier/GTIN code was used on product.
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