Medline Kits containing Zimmer Biomet mixing bowls and… recallZ-2736-2026 · Medline Industries, LP · initiated Jun 10, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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 root cause category: Under Investigation by firm
What the company is doing
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.
Recall details
- Recall number
- Z-2736-2026
- Status
- Open, Classified
- Initiated by the company
- Jun 10, 2026
- Posted by the FDA
- Jul 15, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 163 kits
- Product code
- LRO
- FDA submissions
- K213481
- Distribution
- US Nationwide distribution in the states of CA and UT.
Product description
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
Code information (models, lots, serial numbers)
UDI-DI 10198459538827 Kit Lots 26DMB644 26CMC467
Other devices under the same FDA submission
321 devices cleared under K213481 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Centurion ART690Centurion Medical Products Corporation · General Surgery Tray4 recalls0 reports
- Centurion CVI4505Centurion Medical Products Corporation · General Surgery Tray3 recalls0 reports
- MEDLINE ECVC6355Medline Industries, Inc. · General surgery tray3 recalls0 reports
- MEDLINE ECVC1045Medline Industries, Inc. · General surgery tray3 recalls0 reports
- Centurion ART255Centurion Medical Products Corporation · General surgery tray3 recalls0 reports
- Centurion CVI3880Centurion Medical Products Corporation · General surgery tray3 recalls0 reports
- MEDLINE ECVC1375Medline Industries, Inc. · General surgery tray3 recalls0 reports
- MEDLINE DYNDV2520Medline Industries, Inc. · General surgery tray3 recalls0 reports
- Centurion ST11670ACenturion Medical Products Corporation2 recalls0 reports
- Medline Industries, Inc. ECVC6370Centurion Medical Products Corporation · General Surgery Tray2 recalls0 reports
- MEDLINE ECVC6840Medline Industries, Inc. · General surgery tray2 recalls0 reports
- MEDLINE ECVC6265Medline Industries, Inc. · General Surgery Tray2 recalls0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 99318).
- Z-2737-2026 · Open, ClassifiedMedline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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