Medline Namic Angiographic Control Syringes Recalled Due to Unwinding Risk
Summary
Health Canada has issued a Type I recall for Medline Namic Angiographic Control Syringes due to a risk of the syringe rotating adaptor unwinding during use, which could lead to procedural delays or death. Healthcare professionals are advised to contact the manufacturer for more information and to destroy affected products.
What changed
Health Canada has issued a Type I recall for Medline Namic Angiographic Control Syringes (model numbers 70087007 and 70085007) due to a critical performance issue where the syringe rotating adaptor may unwind during use. This defect poses a significant risk, potentially causing procedural delays and, in severe cases, death.
Healthcare providers and facilities in possession of these syringes are advised to contact Medline Industries, LP for additional information and to destroy the affected products. The recall was initiated on March 25, 2026, with the original publication date also listed as March 27, 2026.
What to do next
- Contact Medline Industries, LP for additional information.
- Destroy affected Medline Namic Angiographic Control Syringes.
Archived snapshot
Mar 27, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Health product recall
Medline Namic Angiographic Control Syringes
Brand(s)
Last updated
2026-03-27
Summary
Product Medline Namic Angiographic Control Syringes Issue Medical devices - Performance What to do Contact the manufacturer if you require additional information.
Audience Healthcare Industry
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Medline Namic Angiographic Control Syringes | More than 10 numbers, contact manufacturer. | 70087007 |
| Medline Namic Angiographic Control Syringes | More than 10 numbers, contact manufacturer. | 70085007 |
Issue
The Namic RA syringes have been recalled by Medline due to a potential risk of the syringe rotating adaptor unwinding during use. If unwinding occurs, it may result in procedural delays, and in severe cases, death. Customers have been advised to destroy these syringes.
Additional information
Details
Original published date:
2026-03-27
Alert / recall type Health product recall Category Health products - Medical devices - Cardiovascular Companies Medline Industries, LP
Three Lakes Drive, Northfield, Illinois, United States, 60093
Published by Health Canada Audience Healthcare Industry Recall class Type I Recall date
2026-03-25
Identification number RA-81802
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Source
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