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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.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) DYNJ50806LUDI-DI: 10195327344672(each)40195327344673(case)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
January 7, 2026
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Product type
Sterilization Kits
Model numbers
1) DYNJ50806L, UDI-DI: 10195327344672(each), 40195327344673(case), Lot Number: 23FBK937
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    January 7, 2026

  2. Reported by FDA DEVICE

    February 25, 2026

  3. RecallRadar source check

    March 4, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

The Medline Convenience Kits are utilized in healthcare settings to provide essential medical supplies in a sterile environment. Consumers and healthcare providers purchase these kits for various medical procedures.

Why This Is Dangerous

Calibration issues with the sterilization equipment may lead to a lack of proper sterilization of medical devices, posing a risk of infection to patients.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall poses a significant health risk, requiring immediate action from users. Patients and healthcare providers must discontinue use and follow the manufacturer's instructions to avoid potential complications.

Practical Guidance

How to identify if yours is affected

  1. Check the model number on the packaging or the product itself.
  2. Confirm if the model number is DYNJ50806L or one of the related UDI-DI numbers.
  3. If the product matches, stop using it immediately.

Where to find product info

The model number and lot number can typically be found on the packaging or on a label attached to the product itself.

What timeline to expect

Expect a refund or replacement process to take approximately 4-6 weeks once the return is initiated.

If the manufacturer is unresponsive

  • Document all communication attempts with Medline Industries.
  • Consider reaching out to regulatory authorities if no response is received.

How to prevent similar issues

  • When purchasing medical devices, always check for the latest recalls and safety notices.
  • Verify that products have appropriate certifications for medical use.
  • Be aware of any recent safety warnings related to sterilization or medical devices.

Documentation advice

Keep copies of all correspondence, receipts, and any documentation related to the product and recall.

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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.

Key Facts

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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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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