Official recall record
Bravo™ - Capsule Delivery Sys
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-06-05
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Medtronic noted an increase in the number and rate of serious injuries during use of the Bravo™ CF Capsule delivery reported between January 2025 and April 2025. The increased number and rate of serious injuries may be attributed to the device's malfunction due to misapplied adhesive. Specifically, the misapplied adhesive may prevent the capsule from attaching to the patient's esophagus or detaching from the delivery device. Recall start date: June 3, 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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