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, 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
- Medical device kit containing Angiographic Rotating Adaptor (RA) Control Syringes
- Model numbers
- Medline SKU # DYNJ63021B, UDI/DI each 10193489833775UDI/DI case 40193489833776, Lot Number: 26AMD887, Medline SKU # DYNJ64297B, UDI/DI each 10198459472992UDI/DI case 40198459472993, Lot Number: 26AMA970, Medline SKU # DYNJ82411, UDI/DI each 10195327193232UDI/DI case 40195327193233 +1 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 are medical convenience kits used with angiographic equipment containing NAMIC Angiographic Rotating Adaptor control syringes. They support procedural workflows in various hospitals worldwide.
Why This Is Dangerous
If the rotating adaptor unwinds, the syringe may detach or loosen from the manifold, potentially disrupting controlled delivery during procedures.
Industry Context
This recall is not described as part of a broader industry pattern in the notice.
Real-World Impact
The recall involves a small quantity (20 kits) but affects critical medical devices used in procedures, requiring immediate cessation of use and follow-up with the manufacturer.
Practical Guidance
How to identify if yours is affected
- Verify kit SKU against DYNJ63021B, DYNJ64297B, DYNJ82411.
- Check lot numbers 26AMD887, 26AMA970, 25IMB049.
Where to find product info
UDI/DI labels on the kit and individual syringes, plus lot numbers on packaging.
What timeline to expect
Refunds or replacements will be issued per recall guidance. Expect several weeks for processing.
If the manufacturer is unresponsive
- Escalate within the hospital's procurement or risk management department.
- Document all communications with Medline and the hospital.
How to prevent similar issues
- Verify UDI/DI and lot numbers before use in future orders.
- Work with distributors to ensure recalls are tracked.
- Maintain updated inventory re: device recalls.
Documentation advice
Keep recall notice, purchase records, lot numbers, and any correspondence.
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Product Details
Recall covers three Medline SKUs: DYNJ63021B (Laparoscopic Herniorrhaphy DSC), DYNJ64297B (LAP PACK), DYNJ82411 (MINOR PROCEDURE PACK). UDI/DI for each unit appears with 10193489833775 and case 40193489833776 for DYNJ63021B; 10198459472992 and case 40198459472993 for DYNJ64297B; 10195327193232 and case 40195327193233 for DYNJ82411. Lot numbers cited: 26AMD887, 26AMA970, 25IMB049. Worldwide distribution includes US and PR and foreign countries (CA, NL, AU, KR, LK, PK, JP, AE, SG, SK). Recall Date: 2026-02-27. Status: ACTIVE. Quantity: 20 kits.
Reported Incidents
No specific incidents or injuries are provided in the recall notice.
Key Facts
- 20 kits recalled (Worldwide distribution)
- Three SKUs affected: DYNJ63021B, DYNJ64297B, DYNJ82411
- Lot numbers: 26AMD887, 26AMA970, 25IMB049
- High hazard level due to potential disconnection
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Safety Guide
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