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, 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 (RA) Control Syringes
- Model numbers
- 1. Medline SKU # DYNJ30880M, UDI/DI each 10198459446207, UDI/DI case 40198459446208, Lot Number: 25LMJ532, 2. Medline SKU # DYNJ64295A, UDI/DI each 10193489353853, UDI/DI case 40193489353854, Lot Number: 24KMI274.
- 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
Medical convenience kits containing NAMIC RA Control Syringes are used in angiography and arthroscopy procedures to manage injectate delivery.
Why This Is Dangerous
Rotating adaptor unwinds during use, creating a loose connection or disconnection between syringe and manifold which may compromise sterile linkage and procedure integrity.
Industry Context
This recall is not explicitly framed as part of a broader industry pattern in the provided data.
Real-World Impact
High risk during surgical or diagnostic procedures if adaptor disengages; impact is procedural integrity and potential sterility concerns.
Practical Guidance
How to identify if yours is affected
- Verify you have one of the two Medline SKUs: DYNJ30880M or DYNJ64295A.
- Check the lot numbers 25LMJ532 or 24KMI274.
Where to find product info
FDA recall page and Medline recall notice provide SKUs, lot numbers, and UDIs.
What timeline to expect
Refund or replacement timelines vary; follow Medline instructions and FDA enforcement communications.
If the manufacturer is unresponsive
- Document all contacts with Medline; escalate to FDA recall contact if needed
- Consider filing a consumer complaint with CPSC if applicable in your jurisdiction
How to prevent similar issues
- Verify device compatibility before procedures
- Maintain an updated inventory of critical surgical adapters
- Establish a recall response plan with procurement and sterile processing teams
Documentation advice
Keep recall notice, verification records, lot numbers, and any correspondence with Medline or healthcare providers
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Product Details
Medline medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes. Two SKUs: 1) DYNJ30880M Shoulder Arthroscopy Pack. 2) DYNJ64295A Extremity Pack. UDI for each: 10198459446207 (single), 40198459446208 (case); Lot numbers 25LMJ532 and 24KMI274. Quantity recalled: 82 kits. Distribution: Worldwide, including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.
Reported Incidents
No incident data provided in the recall notice.
Key Facts
- Two SKUs: DYNJ30880M and DYNJ64295A
- Lot numbers: 25LMJ532 and 24KMI274
- 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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