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 Syringe
- Model numbers
- Medline SKU 60010027, Lot Number 25EBF689, Lot Number 25CBL960, Lot Number 24LBO743, Medline SKU 60010195, Lot Number 25ABI082, Lot Number 24IBJ827, Lot Number 24HBO437 +5 more
- 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
NAMIC Angiographic Syringe is used in angiographic procedures to deliver contrast media. It is distributed widely for hospital and clinic use and spans multiple SKUs and lot numbers.
Why This Is Dangerous
A rotating adaptor may unwind during use, causing a loose or complete disconnection from the manifold. This can compromise the integrity of injections or flush procedures.
Industry Context
This recall is not described as part of a broader industry pattern in the provided notice.
Real-World Impact
Healthcare facilities may need to halt procedures using these syringes. Replacements could affect inventory and procurement timelines.
Practical Guidance
How to identify if yours is affected
- Inspect lot numbers including 25EBF689, 25CBL960, 24LBO743, 25ABI082, 24IBJ827, 24HBO437, 24DBR149, 24CBF820, 26BBJ156, 26ABH642.
- Verify if the product was distributed in your facility or country listed in the recall.
Where to find product info
Recall notifications and serial/lot information are in the FDA enforcement report Z-1717-2026 and Medline recall communications.
What timeline to expect
Refunds or replacements are typically issued within weeks to months after notification. Specific timelines are provided in recall communications.
If the manufacturer is unresponsive
- Escalate to hospital procurement leadership.
- File a formal complaint with Medline and document all interactions.
- Contact the FDA via the recall portal if the manufacturer is unresponsive.
How to prevent similar issues
- Verify supplier recall status before purchasing angiographic syringes.
- Prefer syringes with validated adaptor connections and sterilization records.
- Maintain an up-to-date recall registry for medical devices.
Documentation advice
Keep recall notices, SKU/lot numbers, purchase records, and communication logs. Photograph affected devices and store in a safe location.
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Product Details
Product: NAMIC Angiographic Syringe. Distribution: Worldwide including US, Puerto Rico, Canada, Netherlands, Australia, Korea, Sri Lanka, Pakistan, Japan, UAE, Singapore, Slovakia. Quantity: 149,439 kits. Medline identifiers include SKUs 70075027, 70085007, 70085107, 70087007, 70087107, 70088007, 70095007, 70095107, 70097007, 70097107, 70098107, 80075027, 80085007, 80087007, 80095007, 80095107, 80097107. Hazard type: potential rotation adaptor unwinding leading to loose connection or disconnection between syringe and manifold. Recall date: 2026-02-27. Status: ACTIVE.
Reported Incidents
No incident counts are provided in the summary. The recall is based on post-market surveillance identifying the potential risk.
Key Facts
- 149,439 NAMIC Angiographic Syringe kits recalled worldwide
- Hazard class: Class I
- Rotating adaptor unwinds, causing loose or disconnected syringe-to-manifold connection
- Syringes span multiple SKUs and lot numbers
- US nationwide including PR and international distribution to CA, NL, AU, KR, LK, PK, JP, AE, SG, SK
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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