Quick Facts at a Glance
- Recall Date
- February 27, 2026
- Hazard Level
- HIGH
- Brand
- Medline Industries, LP
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers, Unknown
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL, PREGNANT, PREGNANT
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 VASC1061, UDI/DI each 10889942464722, UDI/DI case 40889942464723, Lot Number 25IBN161, Lot Number 25GBF769, Medline SKU VASC1074, UDI/DI each 10889942611751, UDI/DI case 40889942611752 +6 more
- Sold at
- Multiple Retailers, 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
NAMIC Angiographic Rotating Adaptor syringes are used in angiography procedures to connect syringes to manifolds.
Why This Is Dangerous
An adaptor unwinding during use can loosen or disconnect the syringe from the manifold, potentially affecting sterile technique and patient safety.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects 1,698 kits worldwide. Immediate action is required to prevent potential procedural complications.
Practical Guidance
How to identify if yours is affected
- Check SKU against VASC1061, VASC1074, VASC1198, VASCSHPOFF1, VASCSLPON1.
- Review lot numbers: 25IBN161, 25GBF769, 25HBN798, 25GBL527, 25GDA142.
- Verify UDI/DI details: per-kit and per-unit identifiers.
Where to find product info
FDA enforcement page Z-1715-2026 and Medline recall notices.
What timeline to expect
Remedies will be issued via notification; expect multiple channels. Replacement or refund timelines vary by institution.
If the manufacturer is unresponsive
- Escalate to hospital procurement or regulatory affairs.
- File a formal recall report with Medline and the FDA if delays occur.
How to prevent similar issues
- Verify adaptor connections before use.
- Inspect NAMIC RA syringe kits for secure fittings prior to procedures.
- Implement supplier quality checks for future NAMIC kits.
Documentation advice
Save all recall notices, kit SKUs, lot numbers, and correspondence. Photograph labels and serials for records.
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Product Details
Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Kits include: 1) CSTM MANIFOLD KIT - TITUS, Medline SKU VASC1061; 2) CSTM MANIFOLD KIT - FRYE, Medline SKU VASC1074; 3) CRYO EP MANIFOLD KIT, Medline SKU VASC1198; 4) MANIFOLD KIT - 500PSI OFF, Medline SKU VASCSHPOFF1; 5) MANIFOLD KIT LOW PRESSURE ON, Medline SKU VASCSLPON1. Distribution: Worldwide, including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK. Recall Date: 2026-02-27. Report Date: 2026-04-15. Status: ACTIVE.
Reported Incidents
No incident counts are provided in the available documentation. The recall classification is Class I with high hazard level.
Key Facts
- Syringe RA adaptor unwinds risk
- Loose connection or disconnection between syringe and manifold
- Worldwide distribution including US and PR; CA, NL, AU, KR, LK, PK, JP, AE, SG, SK
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Safety Guide
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