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Medline Recalls 828 Valve Pack-LF Cannula Kits DYNJ0415366P and DYNJ0415366Q (2025)

Medline Industries, LP recalled 828 Valve Pack-LF Cannula Kits DYNJ0415366P and DYNJ0415366Q sold nationwide, including California. The cannula catheter may not retain its shape. Stop using the devices immediately and follow recall instructions for refunds or replacements.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
August 21, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
August 21, 2025
Hazard Level
HIGH
Brand
Medline Industries
Category
Health & Personal Care
Sold At
Unknown
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
Product type
Valve Pack-LF Cannula Kit
Model numbers
DYNJ0415366P, DYNJ0415366Q
Sold at
Unknown
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 21, 2025

  2. Reported by FDA DEVICE

    October 8, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

The kits contain certain lots of cannula products where the catheter may not retain its shape.

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

Valve Pack-LF Cannula Kits are medical device kits used in clinical settings for IV catheterization.

Why This Is Dangerous

The catheter may not retain its shape, potentially compromising performance during use in patient care.

Industry Context

This recall is not identified as part of a broader industry pattern.

Real-World Impact

Hospitals and clinics should screen inventory, halt use of affected units, and coordinate refunds or replacements with Medline.

Practical Guidance

How to identify if yours is affected

  1. Check model numbers DYNJ0415366P or DYNJ0415366Q on the kit.
  2. Review associated lot numbers: 24DMG366 for P; 25EMD672, 25GMD016, 25AMB610, 25BMJ241 for Q.
  3. If any match, set aside for recall remedy.

Where to find product info

Recall notices on the FDA enforcement site and Medline’s recall communications; check the kit packaging for model and lot numbers (UDI where available).

What timeline to expect

Refunds or replacements typically follow the recall process and may take several weeks.

If the manufacturer is unresponsive

  • Escalate to Medline customer service and file a complaint with the FDA if the vendor is slow to respond.
  • Consult hospital risk management for interim patient safety measures.

How to prevent similar issues

  • Verify model and lot numbers before inventory use.
  • Maintain a recall watch for medical devices and establish a process to quarantine affected lots.
  • When purchasing, verify regulatory compliance and supplier recalls.

Documentation advice

Keep the recall letter and FDA notice; photograph packaging and labels; document lot numbers and where the devices were used.

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Product Details

Model numbers: DYNJ0415366P; DYNJ0415366Q. Where sold: US nationwide distribution, with California noted in the recall notice. When sold: Not specified. Price: Not specified. Quantity: 828 units. Recall date: 2025-08-21. Distribution: US nationwide distribution in California. Manufacturer: Medline Industries, LP. Notes: Lot numbers associated with these models are listed below.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Model numbers: DYNJ0415366P, DYNJ0415366Q
  • Lot numbers for P: 24DMG366
  • Lot numbers for Q: 25EMD672, 25GMD016, 25AMB610, 25BMJ241

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
DYNJ0415366P
DYNJ0415366Q
Affected States
ALL
Report Date
October 8, 2025
Recall Status
ACTIVE

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