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 DYNDH1576, UDI/DI 10193489437041, Lot Number 25EBP737, 2) Kit SKU RWM-DC57KC, UDI/DI 10889942582013, Lot Number 25EBE082.
- 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
Medical convenience kits are used in various healthcare settings for procedures requiring sterile supplies. Consumers and healthcare providers rely on these kits for safe and effective medical treatment.
Why This Is Dangerous
The open seal on the BD ChloraPrep Triple Swabsticks can compromise the sterility of the products inside the kit, posing a risk of infection.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall may cause inconvenience for healthcare providers and patients relying on these kits for procedures, necessitating immediate action to ensure safety.
Practical Guidance
How to identify if yours is affected
- Check the SKU number on your kit
- Verify if it's DYNDH1576 or RWM-DC57KC
- Inspect packaging for open seals
Where to find product info
SKU numbers and lot numbers are typically found on the product packaging or accompanying documentation.
What timeline to expect
Expect 4-6 weeks for refund processing after returning the product.
If the manufacturer is unresponsive
- Document all communications with Medline
- Follow up via email or phone
- Consider filing a complaint with the FDA if unresponsive.
How to prevent similar issues
- Always check for seals and packaging integrity before use
- Research medical kit brands for reliability
- Opt for kits with clear labeling and safety certification.
Documentation advice
Keep records of your purchase, any communications with the company, and photographs of the product and its packaging.
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Product Details
The recall includes two specific kits: PowerGlide Dressing Change Kit (SKU DYNDH1576) and Central Line Tray with ChloraPrep SWB (SKU RWM-DC57KC). These kits were distributed nationwide in the U.S.
Key Facts
- Recall date: December 24, 2025
- Quantity recalled: 7,380 kits
- Affected SKUs: DYNDH1576, RWM-DC57KC
- Open seal issue compromises sterility
- No reported injuries yet
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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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