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
- 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
- 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.
Recall announced
August 21, 2025
Reported by FDA DEVICE
October 8, 2025
RecallRadar source check
April 18, 2026
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
- Check model numbers DYNJ0415366P or DYNJ0415366Q on the kit.
- Review associated lot numbers: 24DMG366 for P; 25EMD672, 25GMD016, 25AMB610, 25BMJ241 for Q.
- 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
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Safety Guide
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