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, PREGNANT, PETS
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
- Angiographic Rotating Adaptor (RA) Control Syringes
- Model numbers
- Medline SKU # DYNJ58475F, UDI/DI each 10198459572388, UDI/DI case 40198459572389, Lot Number: 25LMK173, Medline SKU # DYNJ60803J, UDI/DI each 10195327138820, UDI/DI case 40195327138821, Lot Number: 26BMA268 +3 more
- 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
Medical convenience kits containing NAMIC Angiographic Rotating Adaptor control syringes are used in interventional procedures to connect syringes to manifolds in angiography.
Why This Is Dangerous
A rotating adaptor that unwinds can create a loose or complete disconnection between syringe and manifold, risking leakage or device failure.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Immediate action required; health care providers must halt use to avoid potential complications and ensure patient safety.
Practical Guidance
How to identify if yours is affected
- Review Medline NAMIC RA control syringe kits in use.
- Check SKUs DYNJ58475F and DYNJ60803J.
- Inspect UDI codes and Lot Numbers 25LMK173, 26BMA268, 26AMH928, 25EMD876, 25EMA519.
Where to find product info
Refer to FDA enforcement page and Medline recall notices for documentation and steps.
What timeline to expect
Recall could involve replacement or refund processes; timelines vary by region and distributor.
If the manufacturer is unresponsive
- Escalate to hospital risk management.
- File a formal complaint with Medline and the appropriate health authority.
- Seek assistance from procurement/supply chain managers.
How to prevent similar issues
- Verify adaptor integrity before procedures.
- Use only recommended NAMIC RA syringes with compatible manifolds.
- Establish supplier recalls communication to ensure rapid notification.
Documentation advice
Document lot numbers, SKUs, dates of receipt, and communications with Medline or suppliers.
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Product Details
Product: Medline NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. SKUs: DYNJ58475F and DYNJ60803J. UDIs: 10198459572388; 40198459572389; 10195327138820; 40195327138821. Lot numbers: 25LMK173; 26BMA268; 26AMH928; 25EMD876; 25EMA519. Quantity: 439 kits. Sold globally, including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.
Reported Incidents
No injuries or incidents have been reported in the provided data.
Key Facts
- Class I recall
- Worldwide distribution including US and PR
- Syringe adaptor unwind risk
- Loosening or disconnection from manifold
- Lot numbers: 25LMK173, 26BMA268, 26AMH928, 25EMD876, 25EMA519
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Safety Guide
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