Quick Facts at a Glance
- Recall Date
- February 27, 2026
- Hazard Level
- HIGH
- Brand
- Medline Industries, LP
- 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, LP
- Product type
- NAMIC Angiographic Rotating Adaptor (RA) Control Syringes
- Model numbers
- Medline Kit SKU # DYNJ86596, UDI/DI each 10195327656119, UDI/DI case 40195327656110, Lot Numbers: 24FMI029, 24DMK138.
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 27, 2026
Reported by FDA DEVICE
April 15, 2026
RecallRadar source check
April 22, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
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
The Medline NAMIC RA syringe adaptor is used in angiographic procedures as part of a medical convenience kit. The kit groups related tools for catheter-based interventions.
Why This Is Dangerous
If the adaptor unwinds, the syringe may detach or loosen from the manifold, potentially compromising procedure integrity.
Industry Context
This recall is not described as part of a broader industry pattern in the provided notice.
Real-World Impact
Healthcare providers may experience delays or need to replace affected kits, with potential disruption to procedures and workflow.
Practical Guidance
How to identify if yours is affected
- Identify kit SKU DYNJ86596.
- Inspect lot numbers: 24FMI029 or 24DMK138.
Where to find product info
UDI and lot numbers are typically on the kit packaging and the product label.
What timeline to expect
Refunds or replacements follow standard recall processing; confirm with Medline or your facility's biosafety officer.
If the manufacturer is unresponsive
- Document outreach attempts.
- Escalate to the hospital's procurement or risk management department.
- File a report with the supplier and the FDA if needed.
How to prevent similar issues
- Verify rotating adapter components before use.
- Adopt non-rotating alternatives if available.
- Maintain an updated supplier communication channel for recalls.
Documentation advice
Keep the recall notice, purchase records, and any correspondence with Medline or distributors.
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Product Details
Product: NAMIC Angiographic Rotating Adaptor (RA) Control Syringes within Medline medical convenience kits. Kit SKU: DYNJ86596. Distribution: Worldwide, including US, Puerto Rico, Canada, Netherlands, Australia, Korea, Sri Lanka, Pakistan, Japan, United Arab Emirates, Singapore, Slovakia. UDI/DI: 10195327656119 (each), 40195327656110 (case). Lot numbers: 24FMI029 and 24DMK138. Recall date: February 27, 2026. Status: Active. Quantity: 60 kits.
Reported Incidents
No specific injuries or incidents are described in the provided recall notice. The hazard is identified through post-market surveillance.
Key Facts
- 60 kits recalled worldwide
- Kit SKU DYNJ86596
- UDI/DI each 10195327656119
- UDI/DI case 40195327656110
- Lot numbers 24FMI029 and 24DMK138
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Safety Guide
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