FDA recall, , Moderate risk
Medline Kits Containing Zimmer Biomet Mixing Bowls and Spatulas
Medline kits with Zimmer Biomet mixing bowls and spatulas have seal nonconformities risking sterility breach.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, began a recall on June 10, 2026, of Medline Kits containing Zimmer Biomet mixing bowls and spatulas, including TOTAL KNEE PACK DYNJT6267 and TOTAL KNEE PACK-LF DYNJ61651J. The kits contain mixing bowls and spatulas that were recalled due to seal nonconformities, which present a risk of sterility breach.
Health consequences from use include clinically insignificant extension of surgery to find another readily available device. The FDA added the recall to its Enforcement Report and classified it on July 15, 2026, with the weekly enforcement report dated July 22, 2026. Distribution was nationwide in the states of California and Utah.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
2 products
Match the UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Medline Kits containing Zimmer Biomet mixing bowls and spatulas Total Knee Pack DYNJT6267
- UDI-DI
- 10198459538827
- Lot code
- 26DMB644
- 26CMC467
Medline Kits containing Zimmer Biomet mixing bowls and spatulas Total Knee Pack-LF DYNJ61651J
- UDI-DI
- 10195327388447
- Lot code
- 26DME172
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of California and Utah.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Sterility problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99318
- Recall numbers
- Z-2736-2026 to Z-2737-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
