Pro-Dex Inc: Medical Device Recall in 2023 - (Recall #: Z-2098-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver

Product Classification:

Class II

Date Initiated: February 15, 2023

Date Posted: July 12, 2023

Recall Number: Z-2098-2023

Event ID: 92493

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 2000

Code Information:

REF: KLS-BP-001/KLS-BP-040, UDI-DI: 00862377000140, Lot: K0M6U, Expiration: 8/31/2024

Distribution Pattern:

US: FL

Voluntary or Mandated:

Voluntary: Firm initiated