HIGH

Medline Convenience Kits Recalled Due to Sterilization Issues

Medline Industries recalled 32 units of Convenience Kits on January 7, 2026. Issues with sterilization equipment calibration may compromise device safety. Users should stop using the products immediately and follow recall instructions.

Quick Facts at a Glance

Recall Date
January 7, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter

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Product Details

The recalled product includes the Medline Convenience Kits, Model Number DYNJ50806L. These kits were distributed worldwide, including the US, and the recall affects 32 units.

The Hazard

Calibration issues with the sterilization equipment used for these kits may lead to compromised sterility assurance levels. This poses a significant risk to patients and healthcare providers.

Reported Incidents

No specific incidents have been reported related to this recall. However, the potential for compromised sterility could lead to increased health risks.

What to Do

Stop using the Medline Convenience Kits immediately. Contact Medline Industries or your healthcare provider for further instructions on how to proceed with the recall.

Contact Information

For more information, call Medline Industries at 1-800-633-5463 or visit their website at www.medline.com.

Key Facts

  • 32 units recalled
  • Calibration issues may impact sterility
  • Stop using the product immediately
  • Contact Medline for instructions

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
1) DYNJ50806L
UDI-DI: 10195327344672(each)
40195327344673(case)
Lot Number: 23FBK937
Affected States
ALL
Report Date
February 25, 2026
Recall Status
ACTIVE

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