Quick Facts at a Glance
- Recall Date
- December 24, 2025
- 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
- Medical Convenience Kits
- Model numbers
- 1) Kit SKU DT22710, Lot Numbers: 25EBC812, 2) Kit SKU DYNDA1857A, Lot Numbers: 25FBH991, 3) Kit SKU DYNDC1978A, Lot Numbers: 25EBC577, 4) Kit SKU DYNDC2367, Lot Numbers: 25EBS434 +9 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 24, 2025
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
About This Product
Medline medical convenience kits are designed for various medical procedures, providing healthcare professionals with necessary tools and sterile supplies. These kits are commonly used in hospitals and clinics for procedures involving central lines or ports.
Why This Is Dangerous
The potential open seal on the BD ChloraPrep Triple Swabsticks can compromise their sterility, which increases the risk of infection during medical procedures. Sterility is critical for any medical device that comes into contact with open wounds or invasive procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects a significant number of medical kits, posing a potential health risk to patients if used. Healthcare providers must ensure they do not use recalled kits to maintain patient safety.
Practical Guidance
How to identify if yours is affected
- Locate the SKU on your Medline kit packaging.
- Compare the SKU with the recalled list: DT22710, DYNDA1857A, DYNDC1978A, etc.
- Check any lot numbers mentioned in the recall notice.
Where to find product info
SKU and lot numbers can typically be found on the packaging or label of the kit, often near the barcode or product description.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks.
If the manufacturer is unresponsive
- Document all correspondence with Medline Industries.
- Try reaching out again via different methods (phone, email).
- Consider filing a complaint with the FDA if the response is unsatisfactory.
How to prevent similar issues
- Always check for product recalls before purchasing medical supplies.
- Verify the integrity of packaging before use.
- Purchase medical products from reputable sources.
Documentation advice
Keep records of your purchase, including receipts and correspondence regarding the recall for your records.
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
Product Details
Affected products include: Cancer Service Port Kit (SKU DT22710), Line Kit (SKU DYNDA1857A), PICC Removal Kit (SKU DYNDC1978A), and others. Sold nationwide in the U.S. since their distribution.
Key Facts
- Recall date: December 24, 2025
- High hazard level due to potential infection risk
- Total quantity recalled: 7,570 kits
- Affected kit SKUs include DT22710, DYNDA1857A, and others
Browse More Recalls
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 ProductGet Alerts for Health & Personal Care Recalls
Get instant alerts for recalls that affect you. Free forever.