United StatesMedline Kits containing Zimmer Biomet mixing bowls and spatulas — specifically TOTAL KNEE PACK DYNJT6267 and TOTAL KNEE PACK‑LF DYNJ61651J (UDI‑DI 10198459538827, Kit Lots 26DMB644 and 26CMC467; UDI‑DI 10195327388447, Kit Lot 26DME172) are affected. They were recalled because the Zimmer Biomet mixing bowls and spatulas have seal nonconformities that present a risk of sterility breach; health consequences may include a clinically insignificant extension of surgery to find another readily available device.
What's being recalled
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
Recalling firm: Medline Industries, LP, Northfield, IL, United States.
How to identify it
UDI-DI 10198459538827 Kit Lots 26DMB644 26CMC467 UDI-DI 10195327388447 Kit Lot 26DME172
The hazard
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.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the states of CA and UT.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)