HIGHFDA DEVICE

Medline Recalls Medical Kits Over Seal Integrity Issues

Medline Industries, LP recalled 7,380 medical convenience kits on December 24, 2025. The recall affects the PowerGlide Dressing Change Kit and Central Line Tray with ChloraPrep swabsticks. An open seal on packaging may compromise sterility and patient safety.

Official notice
Medline Industries, LPHealth & Personal CareMedical Devices1) Kit SKU DYNDH1576UDI/DI 10193489437041Lot Number 25EBP737

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 24, 2025
Status
ACTIVE
Severity
8/10

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

  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
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.

  1. Recall announced

    December 24, 2025

  2. Reported by FDA DEVICE

    February 18, 2026

  3. RecallRadar source check

    February 25, 2026

  4. 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

  1. Check the SKU number on your kit
  2. Verify if it's DYNDH1576 or RWM-DC57KC
  3. 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.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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

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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

Model Numbers
1) Kit SKU DYNDH1576
UDI/DI 10193489437041
Lot Number 25EBP737
2) Kit SKU RWM-DC57KC
UDI/DI 10889942582013
+1 more
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

Related Recalls