CPSC recall · Reported March 24, 2021
Birdie Belay Devices Recalled Due to Risk of Injury; Made by Beal Sas
The device user can be unable to lower the climber, posing a risk of injury to the climber.
Beal Sas, of France recalled The Beal Birdie Belay Device is used by rock climbers. Belay devices are used with climbi….
Birdie Belay Devices Recalled Due to Risk of Injury; Made by Beal Sas was recalled by Beal Sas, of France in March 24, 2021. Reason: The device user can be unable to lower the climber, posing a risk of injury to the climber.. Remedy: Consumers should immediately stop using the recalled Beal Birdie Belay Devices and contac…. Verify recall #21101 with the CPSC before acting.
The recall
Beal Sas, of France issued this CPSC recall-The device user can be unable to lower the climber, posing a risk of injury to the climber..
- None
- agency class
- March 24, 2021
- reported
Sourced from official CPSC enforcement records. Verify recall #21101 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. Consumers holding this product should act on the agency's documented remedy above rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 41,021 medical devices recalls on record
Product description
The Beal Birdie Belay Device is used by rock climbers. Belay devices are used with climbing ropes to protect the climber while climbing, to arrest a fall or while being lowered on the rope. The Beal Birdie Belay Device was sold in three colors: Orange handle, Blue handle or Green handle. This recall involves all units laser-marked with batch year "/19" on the side of the unit. Only units marked with "/19" are being recalled.
Reason for recall
The device user can be unable to lower the climber, posing a risk of injury to the climber.
Remedy, what to do
Consumers should immediately stop using the recalled Beal Birdie Belay Devices and contact Liberty Mountain for a free replacement.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Not classified by agency |
| Status | Active |
| Recall number | 21101 |
| Date reported | March 24, 2021 |
| Date initiated | March 24, 2021 |
| Recalling firm | Beal Sas, of France |
| Affected scope | About 1,400 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately stop using the recalled Beal Birdie Belay Devices and contact Liberty Mountain for a free replacemen…
- Check the recall number (21101) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Similar severity · nearest report date
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Similar Medical Devices · nearest report date
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Methodology · Corrections · Archive as of August 2026