Use cautionMedical device recall · FDA · Published April 2, 2026
Windstone Medical: Recalled Namic RA Syringes Risk Biohazard Exposure
Windstone Medical recalls Custom Convenience Kits with Medline Namic RA Syringes due to risk of adapter unwinding causing potential biohazard exposure, blood loss, or infection. Affected kits include specific part numbers and lots.
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.
Take action
Contact the company
📍Recalling firmWindstone Medical Packaging, Inc.1602 4th Ave N · Billings, MT 59101-1521
“Windstone Medical: Recalled Namic RA Syringes Risk Biohazard Exposure.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49557-windstone-medical-recalled-namic-ra-syringes-risk-biohazard-exposure. Based on FDA recall #Z-2066-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2066-2026%22&limit=1).
Windstone Medical Packaging, Inc. recalled Custom Convenience Kits containing Medline Namic Angiographic Control Syringes with Rotating Adapter due to a potential biohazard exposure risk, the FDA said on April 2, 2026.
How to tell if you have it
Brand: Windstone Medical
Product: Custom Convenience Kit containing Medline Namic RA Syringes
Distribution: US Nationwide distribution in the state of Arizona
The hazard
The affected kits contain Medline Namic RA Syringes that may have a rotating adapter that unwinds during use, potentially causing a loose connection or full disconnection between the syringe and manifold. This defect poses a risk of biohazard exposure, blood loss, infection, or air embolism.
Context
GovInfoNow's records show Windstone Medical Packaging, Inc. has 14 other recalls on record since Oct. 24, 2017. Other recent recalls of similar products include Windstone AMS Convenience Kit: Blue Break-Off Parts Risk (July 29, 2026), Windstone AMS Angio Pack Kits: Lidocaine Injection Risk (June 17, 2026), and Windstone Medical Packaging Recalls Spine Kits Due to Endotoxin Variability Risk (June 8, 2026). Other recent recalls of similar products include Medline medical convenience kits recall: Risk of syringe rotating adaptor unwinding during use, Medline Medical Kits Recall: Risk of Syringe Disconnection During Use, and Medline Medical Convenience Kits Recall: Risk of Syringe Disconnection (all dated Feb. 27, 2026).
How to tell if you have this one
Check for Custom Convenience Kits with Medline Namic RA Syringes. Affected kits have part numbers AMS6908E or AMS6908F and specific lots listed in the recall notice.
Brand
Windstone Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Syringe Part Numbers
Identify the part numbers on the syringe packaging: AMS6908E or AMS6908F.
Verify Lot Numbers
Check the lot numbers on the packaging: 214875 for AMS6908E or specific lots listed for AMS6908F.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution in the state of Arizona.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 48 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2066-2026 (April 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2066-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.