medical MODERATE Updated 2026-07-22

Medline Industries, LP recalls Medline Kits containing Zimmer Biomet mixing bowls and spatu

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Recalled Product

Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J

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Hazard / Issue

Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include clinically insignificant extension of surgery to find another readily available device.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI 10195327388447 Kit Lot 26DME172

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
View official government recall