Recalling firm
Medline Industries, LP
Product type
Device
Status
Ongoing
Report date
2026-07-22
Distribution
US Nationwide distribution in the states of CA and UT.
Firm state
IL
Product quantity
163 kits
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason 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.
Product description
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
Code / lot info
UDI-DI 10198459538827 Kit Lots 26DMB644 26CMC467
Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.