Zimmer Surgical recalls

5 official recalls and safety alerts involving Zimmer Surgical since 2023-10, 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 Zimmer Surgical or the relevant agency.

  1. 2026-07-08
  2. US
    Drugs & medicalClass II

    Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors Model/Catalog Number:…

    Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find…

    FDA · DeviceZimmer Surgical IncWorldwide distribution - US Nationwide and the countries of Canada and EMEA.Official notice →
  3. 2026-02-04
  4. US
    Drugs & medicalClass II

    Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version:…

    Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.

    FDA · DeviceZimmer Surgical IncInternational distribution to the countries of Canada and EMEA only.Official notice →
  5. 2025-12-24
  6. US
    Drugs & medicalClass II

    Zimmer Surgical Inc recalls Zimmer Air Dermatome, Model/Catalog Number: 00880100100

    The devices may have a misaligned thickness control bar.

    FDA · DeviceZimmer Surgical IncDistribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia,…Official notice →
  7. 2024-02-21
  8. US
    Drugs & medicalClass II

    Zimmer Surgical Inc recalls 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

    Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary.

    FDA · DeviceZimmer Surgical IncWorldwide - US Nationwide distribution including in the states of CA, DE, FL,…Official notice →
  9. 2023-10-11
  10. US
    Drugs & medicalClass II

    Zimmer Surgical Inc recalls Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that…

    Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area

    FDA · DeviceZimmer Surgical IncUS Nationwide Foreign: AUSTRALIA BRAZIL CHINA HONG KONG INDIA JAPAN MALAYSIA…Official notice →