Severity
Moderate
ModerateActive
CPSC recall · Reported June 23, 2009
Diving Wings With Defective Inner Bladders Recalled by Poseidon Due to Drowning Hazard
The inner bladder located inside the diving wing can break, causing the wing to fail to operate as a floating/buoyancy device. This poses a drowning hazard to divers.
Compiled from official public sources by the editorial team.
Verify with CPSC →
Poseidon West, of West Lake Village, Calif. recalled The recall involves the Poseidon inner bladders with batch number 5445 sold with the Pose… - a moderate-severity action.
Diving Wings With Defective Inner Bladders Recalled by Poseidon Due to Drowning Hazard was recalled by Poseidon West, of West Lake Village, Calif. in June 23, 2009. Reason: The inner bladder located inside the diving wing can break, causing the wing to fail to operate as a floating…. Remedy: Consumers who have wings that contain the recalled inner bladders should stop using the w…. Verify recall #09251 with the CPSC before acting.
The recall
Poseidon West, of West Lake Village, Calif. issued this moderate-severity CPSC recall-The inner bladder located inside the diving wing can break, causing the wing to fail to operate as a floating….
- Moderate
- severity level
- June 23, 2009
- reported
Sourced from official CPSC enforcement records. Verify recall #09251 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #09251) was formally reported on June 23, 2009. It is classified under Moderate severity, with a current status of Active. Poseidon West, of West Lake Village, Calif. is listed as the recalling firm. Federal records list the affected scope as About 300.
The documented reason for this recall is: The inner bladder located inside the diving wing can break, causing the wing to fail to operate as a floating/buoyancy device. This poses a drowning hazard to divers. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers who have wings that contain the recalled inner bladders should stop using the wing immediately and contact Poseidon for a free replacement. - consumers holding this product should act on that instruction rather than relying on general guidance.
Within the same product category the archive holds 6 closely related recalls, 3 from CPSC - 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 - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 300
Related Recalls
6
3 from same agency
Product description
The recall involves the Poseidon inner bladders with batch number 5445 sold with the Poseidon Besea W50 wings. The inner bladder is located inside the outer cover of the wing. The batch number and "Poseidon" are molded on a tab located between the "legs" of the inner bladder.
Reason for recall
The inner bladder located inside the diving wing can break, causing the wing to fail to operate as a floating/buoyancy device. This poses a drowning hazard to divers.
Remedy, what to do
Consumers who have wings that contain the recalled inner bladders should stop using the wing immediately and contact Poseidon for a free replacement.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 09251 |
| Date reported | June 23, 2009 |
| Date initiated | June 23, 2009 |
| Recalling firm | Poseidon West, of West Lake Village, Calif. |
| Affected scope | About 300 |
| 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 who have wings that contain the recalled inner bladders should stop using the wing immediately and contact Poseidon for…
- Check the recall number (09251) 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.
Frequently Asked Questions
What product was recalled? ▼
The recall involves the Poseidon inner bladders with batch number 5445 sold with the Poseidon Besea W50 wings. The inner bladder is located inside the outer cover of the wing. The batch number and "Poseidon" are molded on a tab located between the "legs" of the inner bladder.. Recalled by Poseidon West, of West Lake Village, Calif.. Units affected: About 300.
Why was this product recalled? ▼
The inner bladder located inside the diving wing can break, causing the wing to fail to operate as a floating/buoyancy device. This poses a drowning hazard to divers.
What should consumers do? ▼
Consumers who have wings that contain the recalled inner bladders should stop using the wing immediately and contact Poseidon for a free replacement.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 23, 2009. Severity: Moderate. Recall number: 09251.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (09251) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: CPSC, reported June 23, 2009. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.