Medline Angiographic Kit Recall - Syringe Adaptor Unwinding Risk
Summary
Health Canada issued a Type I recall for Medline Namic Custom Angiographic Kits (catalog numbers 60700513, 60701152, 60700465) due to potential risk of the syringe rotating adaptor unwinding during use, which may cause procedural delays or death. Healthcare facilities must immediately stop using affected Namic RA Syringes and discard them. Recall identification number RA-81841.
What changed
Health Canada has issued a Type I recall for Medline Namic Custom Angiographic Kits containing Namic Angiographic Rotating Adaptor (RA) Control Syringes. The recall is due to a potential risk that the syringe rotating adaptor may unwind during use, which could cause procedural delays and, in severe cases, death. Three catalog numbers are affected (60700513, 60701152, 60700465), with multiple lot numbers requiring manufacturers to be contacted for specific identification.
Healthcare providers must immediately stop using Namic RA Syringes from the affected kits and discard them from further use. Facilities should contact the manufacturer for additional information and to determine if they have affected products. No specific compliance deadline is stated, but this is classified as a Type I recall indicating serious potential risk to health, requiring immediate action.
What to do next
- Stop using and discard all Namic RA Syringes from affected angiographic kits immediately
- Contact Medline Industries to determine if your facility has affected lots
- Report any adverse events or device failures related to this recall to Health Canada
Archived snapshot
Apr 3, 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 Custom Angiographic Kit
Brand(s)
Last updated
2026-04-07
Summary
Product Medline Namic Custom Angiographic Kit Issue Medical devices - Performance What to do Contact the manufacturer if you require additional information.
Audience Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
| --- | --- | --- |
| Namic Custom Angiographic Kit | More than 10 numbers, contact manufacturer. | 60700513 |
| Namic Custom Angiographic Kit | More than 10 numbers, contact manufacturer. | 60701152 |
| Namic Custom Angiographic Kit | More than 10 numbers, contact manufacturer. | 60700465 |
Issue
Kits containing Namic Angiographic Rotating Adaptor (RA) Control Syringes (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, in severe cases, death. Customers have been advised to discard these syringes, from the kit, from further use.
Additional information
Details
Original published date:
2026-04-02
Alert / recall type Health product recall Category Health products - Medical devices - Cardiovascular Companies Medline Industries, LP
Published by Health Canada Audience Healthcare Recall class Type I Recall date
2026-04-02
Identification number RA-81841
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