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
- 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
- NAMIC Angiographic Rotating Adaptor (RA) Control Syringes
- Model numbers
- Medline SKU 00-HCT055P, UDI/DI each 10193489297393, UDI/DI case 40193489297394, Lot Number 24BBI341, Lot Number 23LBP066, Lot Number 23KBS305, Lot Number 23JBA062, Lot Number 23HBR594
- Sold at
- Multiple Retailers
- 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
Medline medical convenience kits bundle NAMIC angiographic components used in interventional cath lab procedures. These kits aid procedural setup and delivery of contrast or medications via angiographic systems.
Why This Is Dangerous
The adaptor may unwind, loosening the syringe-to-manifold connection. A loose or disconnected connection can compromise device integrity during procedures.
Industry Context
This recall is part of post-market surveillance in medical devices. Not described as a broader pattern in the provided data.
Real-World Impact
Healthcare providers may need to halt certain procedures until replacement kits are obtained, potentially affecting workflow and patient safety.
Practical Guidance
How to identify if yours is affected
- Identify affected NAMIC RA syringe kits within Medline SKUs listed.
- Check UDI codes 10193489297393 and case code 40193489297394.
- Review lot numbers 24BBI341, 23LBP066, 23KBS305, 23JBA062, 23HBR594.
Where to find product info
Recall notices from Medline and FDA enforcement page Z-1716-2026. Manufacturer communications will include instructions.
What timeline to expect
Refunds or replacements typically processed within weeks; follow manufacturer's instructions for next steps.
If the manufacturer is unresponsive
- Escalate to hospital risk management.
- File a report with the local medical device regulator if necessary.
- Document all communications and preserve the recalled kits as instructed.
How to prevent similar issues
- Verify SKUs and UDIs before purchasing interventional kits.
- Maintain an inventory control process to isolate recalled lots.
- Establish alternate suppliers for critical angiography components.
Documentation advice
Document model numbers, lot numbers, UDI, purchase records, and all recall communications.
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Product Details
Recall involves NAMIC Angiographic Rotating Adaptor control syringes included in Medline medical convenience kits. Distribution spans US, PR, and international markets including CA, NL, AU, KR, LK, PK, JP, AE, SG, SK. 10 Medline SKUs listed. 17902 kits recalled. Recall date 2026-02-27. Report date 2026-04-15.
Reported Incidents
No specific injuries or incidents are provided in the recall notice. The hazard is described as a potential risk identified through surveillance.
Key Facts
- 17902 kits recalled worldwide
- 10 Medline SKUs affected
- Syringe RA adaptor unwinding risk
- Loose connection or disconnection between syringe and manifold
- Class I recall
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Safety Guide
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