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 Syringe Kit
- Model numbers
- Medline SKU # DYNJ68037C, UDI/DI each 10198459239328, UDI/DI case 40198459239329, Lot Number: 25HBV397, Medline SKU # DYNJ89845, UDI/DI each 10198459292460, UDI/DI case 40198459292461, Lot Number: 25CBU222 +6 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 angiographic procedures to connect syringe to a manifold. These are packaged in medical convenience kits.
Why This Is Dangerous
The adaptor could unwind during use, causing a loose connection or full disconnection between syringe and manifold, potentially compromising sterile technique or introducing leaks.
Industry Context
This recall is not described as part of a broader industry pattern in the provided data.
Real-World Impact
The recall affects patient safety during interventional procedures and may require kit replacement during clinical workflows.
Practical Guidance
How to identify if yours is affected
- Locate Medline SKUs DYNJ68037C, DYNJ89845, DYNJ89845A in your stock or records
- Check associated UDI numbers and lot codes listed in the recall documents
- Verify packaging and labeling against recall notice
Where to find product info
FDA enforcement page Z-1719-2026; Medline recall communications with physicians and distributors
What timeline to expect
Refunds or replacements to be arranged through Medline recall process; timelines not specified in the provided data
If the manufacturer is unresponsive
- Escalate to hospital purchasing department
- File a complaint with Medline corporate consumer safety
- Contact FDA or CPSC recall information lines for guidance
How to prevent similar issues
- Implement supplier lot tracking to detect affected lots quickly
- Verify adaptor integrity before use in any angiography kit
- Maintain sterile technique and immediate discard if adaptor appears unsecured
- Stay updated with Medline recall alerts for future actions
Documentation advice
Keep recall notice, lot numbers, UDI codes, and correspondence with Medline; document kit disposal or replacement steps
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Product Details
Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Labeled as: 1) NON VASCULAR PACK, Medline SKU DYNJ68037C; 2) VEIN, Medline SKU DYNJ89845; 3) VEIN, Medline SKU DYNJ89845A. Distributed worldwide including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.
Reported Incidents
No specific incidents or injuries were detailed in the provided information. The recall is categorized as Class I with a high hazard designation.
Key Facts
- Class I recall
- Global distribution including US and PR
- Medline SKU DYNJ68037C
- Medline SKU DYNJ89845
- Medline SKU DYNJ89845A
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Safety Guide
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