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, 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
- Syringe/Angiography Kit Adaptor
- Model numbers
- Medline SKU # 60010508, UDI/DI each 10193489040340, UDI/DI case 40193489040341, Lot Number: 26BBI625, Lot Number: 26ABB718, Lot Number: 25JBJ140, Lot Number: 25HBF702, Lot Number: 25GBC747
- 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
Medline NAMIC RA syringes are used in angiography and related surgical packs within extensive MEDLINE kits.
Why This Is Dangerous
The rotating adaptor could unwind, creating a loose connection or disconnection with the manifold and potentially affecting device performance.
Industry Context
This recall is not clearly indicated as part of a broader industry pattern in the provided data.
Real-World Impact
Immediate halting of use for affected kits; potential impact on procedural accuracy and safety; costs related to replacement.
Practical Guidance
How to identify if yours is affected
- Identify Medline SKU numbers listed in the recall.
- Inspect lot numbers 26BBI625, 26ABB718, 25JBJ140, 25HBF702, 25GBC747.
Where to find product info
FDA recall page and Medline notice; contact healthcare providers for guidance.
What timeline to expect
Replacement or refunds will be issued per Medline instructions; timeline not specified.
If the manufacturer is unresponsive
- Escalate to hospital procurement or distributor.
- Maintain documentation of attempts to contact Medline.
How to prevent similar issues
- Verify syringe adaptor integrity before use.
- Follow vendor instructions for replacement kits.
- Track lot numbers during inventory management.
Documentation advice
Keep recall notice, purchase records, and any adverse event reports; photograph affected SKUs and lot codes.
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Product Details
Recall involves NAMIC Angiographic Rotating Adaptor (RA) Control Syringes distributed within Medline medical convenience kits. 79843 units recalled. Medline SKU variants include 60010508 and numerous other SKUs listed in the recall. UDI/DI: 10193489040340 (per case) and 40193489040341 (per case). Lot numbers include 26BBI625, 26ABB718, 25JBJ140, 25HBF702, 25GBC747.
Reported Incidents
No specific injuries or incidents are detailed in the provided data.
Key Facts
- Worldwide distribution including US, PR and foreign countries (CA, NL, AU, KR, LK, PK, JP, AE, SG,SK
- Syringe adaptor unwinding risk leads to loose/disconnected connections
- UMIs: 10193489040340 (UDI/DI per case) and 40193489040341 (UDI/DI per case)
- Lot numbers: 26BBI625, 26ABB718, 25JBJ140, 25HBF702, 25GBC747
- Class I recall—highest risk category
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Safety Guide
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