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
- Angiography Instrumentation/Syringes
- Model numbers
- Medline SKU DYNJ42367B UDI/DI each 10193489211511, UDI/DI case 40193489211512, Lot Numbers: 24FBJ579, 24DBL828, 24DBE055, 24CBG967, 24ABN254, 23LBI540 +9 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
These kits are used to perform angiography procedures. They include syringes with NAMIC Angiographic Rotating Adaptor to connect syringes to a manifold.
Why This Is Dangerous
If the adaptor unwinds, it can create a loose or disconnected connection, potentially affecting sterile pathways during procedures.
Industry Context
This recall is not indicated as part of a broader pattern; it reflects post-market surveillance findings specific to this product line.
Real-World Impact
High risk during critical medical procedures; urgent action required to stop use and contact Medline for instructions.
Practical Guidance
How to identify if yours is affected
- Verify Medline SKU DYNJ42367B CVOR ANGIOGRAPHY PACK-LF
Where to find product info
FDA enforcement page Z-1714-2026 and Medline recall communications
What timeline to expect
Refunds or replacements are typically addressed within weeks to months after notification
If the manufacturer is unresponsive
- Escalate to Medline customer service
- File a report with the FDA if necessary
- Consult healthcare provider for guidance
How to prevent similar issues
- Verify supplier recalls before procurement
- Maintain incident reporting with PPID
- Use only calibrated NAMIC RA adaptors from authorized channels
Documentation advice
Keep recall notices, purchase records, and all communications; photograph kit and labels for records
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Product Details
Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Labeled CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B. Quantity: 3120 kits. Distribution: Worldwide, including US, Puerto Rico, and international markets (CA, NL, AU, KR, LK, PK, JP, AE, SG, SK).
Reported Incidents
No specific injuries or incidents are reported in the provided data.
Key Facts
- Worldwide distribution including US and PR
- Labeled CVOR ANGIOGRAPHY PACK-LF
- Medline SKU DYNJ42367B
- UDIs and multiple lot numbers listed
- High risk following post-market surveillance
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Safety Guide
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