Medline Convenience Kits Recall
See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) BREAST-HERNIA-PORT CDS-LF, Mode
Updated January 7, 2026
Medline is recalling multiple surgical convenience kits due to sterilization equipment calibration issues that may have compromised the sterility of these devices. Using non-sterile surgical instruments and materials carries a serious infection risk.
Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on January 7, 2026. Details below.
What is recalled
Medline Convenience Kits with the following model numbers: ACC010499 (Plastic Bin with Misc Kits), CDS984853J (Breast-Hernia-Port), DYKMBNDL117C (Urology Urethroplasty Kit), DYKMBNDL158 (Plastic Insert Tissue Expansion Kit), DYKMBNDL170, DYKMBNDL170A, DYKMBNDL170B, and DYKMBNDL182 (Abdominoplasty Kits).
Am I affected
You are affected if you are a healthcare facility or surgical center that received or used any Medline Convenience Kit with one of these model numbers: ACC010499, CDS984853J, DYKMBNDL117C, DYKMBNDL158, DYKMBNDL170, DYKMBNDL170A, DYKMBNDL170B, or DYKMBNDL182.
What to do right now
Stop using these kits immediately. Contact Medline Industries or your healthcare distributor to arrange return or replacement of the recalled items. Check your inventory now against the model numbers listed above.
The hazard
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-2099-2026
- Classification
- Class II
- Recalled
- January 7, 2026
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