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Pro-dex Inc Recalls

5 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Pro-dex Inc.

5Total Recalls
0Critical
6,257Units Affected
Sep 23, 2024Most Recent
All Recalls

Every Pro-dex Inc Recall

Sorted by most recent. Click any recall for full details.

5 recalls
High RiskFDA
Pro-dex Inc
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 surgi...
Surgical Devices·2,000 affected·Sep 23, 2024
High RiskFDA
Pro-dex Inc
KLS 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 d...
Medical Devices·199 affected·Feb 14, 2023
High RiskFDA
Pro-dex Inc
PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches -...
Surgical Devices·68 affected·Sep 25, 2018
High RiskFDA
Pro-dex Inc
Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
Surgical Devices·1,995 affected·Dec 23, 2015
High RiskFDA
Pro-dex Inc
Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdr...
Surgical Devices·1,995 affected·Dec 23, 2015