HIGHFDA DEVICE

Medline NAMIC Angiographic Adaptor Syringe Recall Expands Worldwide in 240 Kits (Class I)

Medline Industries, LP recalled 240 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers worldwide distribution including the US, Puerto Rico, and multiple international markets. The potential issue is the adaptor unwinding during use, risking a loose connection or disconnection with the manifold.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesMedline SKU # DYNJ63673DUDI/DI each 10195327304843UDI/DI case 40195327304844

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
February 27, 2026
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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 # DYNJ63673D, UDI/DI each 10195327304843, UDI/DI case 40195327304844, Lot Number: 25GLA141
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    February 27, 2026

  2. Reported by FDA DEVICE

    April 15, 2026

  3. RecallRadar source check

    April 22, 2026

  4. 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 medical procedures requiring precise delivery through manifolds.

Why This Is Dangerous

If the adaptor unwinds, connections can loosen or disconnect, potentially complicating procedures and compromising sterility.

Industry Context

This recall is not identified as part of a broader industry pattern.

Real-World Impact

Immediate cessation of use; potential medical procedure delays or complications if a kit is in use.

Practical Guidance

How to identify if yours is affected

  1. Verify Medline SKU DYNJ63673D on the kit label.
  2. Check UDI 10195327304843 for individual units and case UDI 40195327304844.
  3. Look for Lot Number 25GLA141.

Where to find product info

Official recall notice and FDA enforcement report linked in the recall page.

What timeline to expect

Refunds or replacements will be processed per Medline recall procedures; timeline not specified.

If the manufacturer is unresponsive

  • Document all attempts to contact Medline.
  • Escalate to the facility's supplier representative or regulatory body if needed.

How to prevent similar issues

  • Verify device compatibility with manifolds before use.
  • Monitor post-market surveillance for similar issues.
  • Maintain strict inventory control to isolate affected SKUs.

Documentation advice

Keep all recall communications, batch details, and replacement receipts for records.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

Model numbers and identifiers: Medline SKU # DYNJ63673D. UDI/DI (individual) 10195327304843. UDI/DI (case) 40195327304844. Lot Number: 25GLA141. Quantity: 240 kits. Sold worldwide including US, PR, CA, NL, AU, KR, LK, PK, JP, AE, SG, SK.

Reported Incidents

No incident numbers are provided in the recall notice. The status is ACTIVE with a HIGH hazard level.

Key Facts

  • Class I recall
  • Adaptor unwinds risking loose connection
  • Syringe and manifold disconnection
  • Worldwide distribution including US and PR
  • Medline SKU DYNJ63673D

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETS
Injury Types
ELECTRICALLACERATIONPOISONINGSUFFOCATIONOTHER

Product Classification

Product Details

Model Numbers
Medline SKU # DYNJ63673D
UDI/DI each 10195327304843
UDI/DI case 40195327304844
Lot Number: 25GLA141
Affected States
ALL
Report Date
April 15, 2026
Recall Status
ACTIVE

Related Recalls