Class II
Medical Device Recall: Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
Medline Industries, LP · June 10, 2026
Reason for Recall
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.
Distribution
US Nationwide distribution in the states of CA and UT.
States Affected
NATIONWIDE
Quantity Affected
163 kits
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2737-2026
Status: ongoing
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