Recall Atlas

Pro-Dex recalls

3 official recalls and safety alerts involving Pro-Dex since 2023-04, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Pro-Dex or the relevant agency.

  1. 2024-11-06
  2. US
    Drugs & medicalClass II

    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 MaxDriver 2.0…

    The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package.

    FDA · DevicePro-Dex IncUS distribution to FL only.Official notice →
  3. 2023-07-12
  4. US
    Drugs & medicalClass II

    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 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…

    FDA · DevicePro-Dex IncUS: FLOfficial notice →
  5. 2023-04-26
  6. US
    Drugs & medicalClass II

    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.g. drill) to a…

    Incorrect Unique Device Identifier/GTIN code was used on product.

    FDA · DevicePro-Dex IncU.S. Nationwide distribution in the state of FL.Official notice →