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
- NAMIC Angiographic Rotating Adaptor (RA) Control Syringes
- Model numbers
- Medline SKU # DYNJ57032D, UDI/DI each 10198459183850, UDI/DI case 40198459183851, Lot Number: 25HBN999, Lot Number: 25HBO039, Medline SKU # DYNJ64026C, UDI/DI each 10195327550059, UDI/DI case 40195327550050 +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
NAMIC Angiographic Rotating Adaptor syringes are used in interventional radiology to connect syringes to a manifold during procedures.
Why This Is Dangerous
The adaptor may unwind, creating a loose connection or disconnection and potential exposure to fluids or failure of the delivery system.
Industry Context
This recall is not described as part of a broader industry pattern in the provided data.
Real-World Impact
The recall presents a high risk to procedures if connections fail, potentially delaying critical interventions.
Practical Guidance
How to identify if yours is affected
- Check SKU numbers against ANGIO PACK DYNJ57032D, NEURO INTERVENTIONAL RADIOLOGY DYNJ64026C, NEURO INERVENTIONAL RADIOLOGY VASC1650.
- Inspect lot numbers: 25HBN999, 25HBO039, 24JBC741, 24IBM270, 24IBE756.
Where to find product info
UDI on the product label and packaging; lot numbers printed on the device packaging.
What timeline to expect
Replacements or refunds processed per Medline recall communications; typical timelines not specified.
If the manufacturer is unresponsive
- Document all outreach attempts.
- Contact hospital administration or device supply chain manager for escalation.
- File complaints with the FDA if applicable.
How to prevent similar issues
- Verify device compatibility before procedures.
- Maintain updated recall notices in procurement systems.
- Request supplier confirmations on safety notices.
Documentation advice
Keep recall notices, serial numbers, lot numbers, and correspondence with Medline and healthcare providers.
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Product Details
Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Labeled: ANGIO PACK, Medline SKU DYNJ57032D; NEURO INTERVENTIONAL RADIOLOGY, SKU DYNJ64026C; NEURO INERVENTIONAL RADIOLOGY, SKU VASC1650. UDI/DI each 10198459183850; case 40198459183851. Lot numbers: 25HBN999, 25HBO039, 24JBC741, 24IBM270, 24IBE756. Distribution: Worldwide, including US, Puerto Rico, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.
Reported Incidents
No specific incidents or injuries cited in the provided data. The status is active with high hazard level based on post-market surveillance.
Key Facts
- Global distribution including US, PR and multiple countries listed
- Labeled SKUs: DYNJ57032D, DYNJ64026C, VASC1650
- UDI/DI numbers provided for each unit and case
- Lot numbers: 25HBN999, 25HBO039, 24JBC741, 24IBM270, 24IBE756
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Safety Guide
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