Pro Dex recalls
Pro Dex appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2024-11-06.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- 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 surgica…
FDA Device · Class II · 2024-11-06 · Pro Dex - KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
FDA Device · Class II · 2023-07-12 · Pro Dex - 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 driver…
FDA Device · Class II · 2023-04-26 · Pro Dex - PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDB…
FDA Device · Class II · 2019-08-28 · Pro Dex - Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver)
FDA Device · Class II · 2016-03-23 · Pro Dex - Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver)
FDA Device · Class II · 2016-03-23 · Pro Dex