Pro-Dex Recalls
6 recalls on record · March 23, 2016 to November 6, 2024 · Medical Devices
Recalls by year
16
19
23
24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 6, 2024Medical DevicesFDA
Pro-Dex Inc recalls KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin Ma
Hazard: The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package.
July 12, 2023Medical DevicesFDA
Pro-Dex Inc recalls KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxD
Hazard: 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.
April 26, 2023Medical DevicesFDA
Pro-Dex Inc recalls KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e
Hazard: Incorrect Unique Device Identifier/GTIN code was used on product.
August 28, 2019Medical DevicesFDA
Pro-Dex Inc recalls PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery P
Hazard: Visual particulates within a battery Tyvek pouch. The battery is provided sterile for use with surgical drivers.
March 23, 2016Medical DevicesFDA
Pro-Dex Inc recalls Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgica
Hazard: The sterile battery may contain particulates within the sterile package.
March 23, 2016Medical DevicesFDA
Pro-Dex Inc recalls Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered
Hazard: The sterile battery may contain particulates within the sterile package.