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
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
- Medline SKU # DYNJ42892F, UDI/DI each10195327693718, UDI/DI case 40195327693719, Lot Number : 25GMD696, Lot Number : 25EMJ573, Lot Number : 25DMC646, Lot Number : 25BMD630, Lot Number : 24LMA523
- 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
Medline NAMIC Angiographic Rotating Adaptor syringes are typically used in interventional radiology to connect syringes to angiographic manifolds. They are part of medical kits distributed to healthcare facilities.
Why This Is Dangerous
The rotating adaptor may unwind during use, creating a loose or complete disconnection between syringe and manifold, which could compromise the sterile pathway or delivery.
Industry Context
This recall is not clearly identified as part of a broader industry pattern in the provided data.
Real-World Impact
Healthcare facilities may need to replace affected kits; no injuries reported yet.
Practical Guidance
How to identify if yours is affected
- Check SKUs DYNJ42892F and DYNJ42892G
- Verify UDI/DI: 10195327693718 (individual) and 40195327693719 (case)
- Inspect lot numbers: 25GMD696, 25EMJ573, 25DMC646, 25BMD630, 24LMA523
- Review distribution list for facilities that received kits
Where to find product info
FDA enforcement page linked in recall notice for instructions
What timeline to expect
Refunds/replacements timelines determined by Medline; typical medical device recalls take weeks to months
If the manufacturer is unresponsive
- Escalate to Medline customer service
- File a report with hospital risk management
- Contact FDA/CMC for guidance
How to prevent similar issues
- Verify device integrity before use
- Follow manufacturer guidelines for inspection
- Keep documentation of lot numbers and SKUs for future recalls
- Consider alternative NAMIC RA syringe products if approved by hospital procurement
Documentation advice
Maintain recall notification, stock records, correspondence, and any replacement documentation
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Product Details
Recall covers Medline NAMIC Angiographic Rotating Adaptor (RA) Control Syringes in medical convenience kits. SKUs: DYNJ42892F and DYNJ42892G. UDI/DI: 10195327693718. Case UDI/DI: 40195327693719. Lot numbers: 25GMD696, 25EMJ573, 25DMC646, 25BMD630, 24LMA523. Quantity: 966 kits. Distribution: Worldwide including US, Puerto Rico, Canada, Netherlands, Australia, Korea, Sri Lanka, Pakistan, Japan, United Arab Emirates, Singapore, Slovakia.
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Syringe rotating adaptor unwinds risk
- DYNJ42892F and DYNJ42892G SKUs
- Lot numbers: 25GMD696, 25EMJ573, 25DMC646, 25BMD630, 24LMA523
- Global distribution including US and PR; 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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