Recall Z-2737-2026

Medline Industries, LP · initiated June 10, 2026

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

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

Codes / lots: UDI-DI 10195327388447 Kit Lot 26DME172

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.

FDA-determined cause: Under Investigation by firm

Action taken

On June 10, 2026, the firm began notifying customers via First-Class Mail and email. Customers were instructed to request stickers to over-label the affected convenience kits with a label indicating to remove the affected component and replace it with product from supply. No kits are to be returned.

Details

Recall number
Z-2737-2026
Initiated
June 10, 2026
Posted by FDA
July 15, 2026
Product code
OJH – Orthopedic Tray
Quantity
163 kits
Distribution
US Nationwide distribution in the states of CA and UT.
Recalling firm
Medline Industries, LP, Northfield, IL

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2736-2026 Class IIMedline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which… 06/10/2026Open, Classified