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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 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) DYKA1343A, UDI-DI: 10193489312966(each), 40193489312967(case), Lot Number: 25LBC732, 2) DYKA1343A, Lot Number: 25FBN781, 3) DYKA1343A, Lot Number: 25DBK346 +4 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 7, 2026
Reported by FDA DEVICE
February 25, 2026
RecallRadar source check
March 4, 2026
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 ADMIT KIT is used in healthcare settings for patient admission procedures. These kits typically include various sterile medical devices necessary for initial patient care.
Why This Is Dangerous
The calibration issues in the sterilization equipment may lead to inadequate sterilization of the kits, increasing the risk of infection for patients.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers and healthcare providers face potential health risks from using non-sterile kits. Immediate action is necessary to prevent possible infections.
Practical Guidance
How to identify if yours is affected
- Locate the model number DYKA1343A on your kit.
- Check the lot numbers against the affected list: 25LBC732, 25FBN781, 25DBK346, 24IBD021, 24DBK171.
- If your kit matches, it is subject to the recall.
Where to find product info
Model and lot numbers are typically printed on the packaging or on the kit itself.
What timeline to expect
Expect a timeframe of 4-6 weeks for refund processing after following the recall instructions.
If the manufacturer is unresponsive
- Follow up with Medline Industries via phone or email.
- Contact consumer protection agencies if the issue remains unresolved.
How to prevent similar issues
- Always check for product recalls before using medical devices.
- Look for certifications indicating proper sterilization processes in future purchases.
- Consult healthcare providers about the safety of medical devices before use.
Documentation advice
Document your communications regarding the recall, including dates and details of your interactions.
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Product Details
The recalled ADMIT KITS have model number DYKA1343A and include several lot numbers: 25LBC732, 25FBN781, 25DBK346, 24IBD021, and 24DBK171. The products were distributed worldwide, including across the United States, and were sold in multiple healthcare settings.
Key Facts
- Recall date: January 7, 2026
- Class II recall classification
- Total quantity recalled: 1,070 units
- Worldwide distribution including US
- Lot numbers affected: 25LBC732, 25FBN781, 25DBK346, 24IBD021, 24DBK171
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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