Official recall record
IMPRA® Carboflo™ Flex Carbon-Lined
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-03-13
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
One lot of IMPRA® Carboflo™ Flex 10 mm x 50 cm, product catalog code F5010C, lot number VTHV0076, was discovered to be missing the removable spiral reinforcement material (beading) that should be present on the product. Recall start date: March 4, 2025
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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