Severity
Moderate
ModerateActive
CPSC recall · Reported June 5, 2013
DiveAlert Emergency Signaling Devices Recalled by Ideations Due to Drowning Hazard
The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard.
Ideations DiveAlert, of Seattle, Wash. recalled This recall involves DiveAlert and DiveAlert PLUS scuba dive signaling devices with model… - a moderate-severity action.
DiveAlert Emergency Signaling Devices Recalled by Ideations Due to Drowning Hazard was recalled by Ideations DiveAlert, of Seattle, Wash. in June 5, 2013. Reason: The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard.. Remedy: Consumers should immediately stop using the recalled DiveAlert signaling devices and retu…. Verify recall #13207 with the CPSC before acting.
The recall
Ideations DiveAlert, of Seattle, Wash. issued this moderate-severity CPSC recall-The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard..
- Moderate
- severity level
- June 5, 2013
- reported
Sourced from official CPSC enforcement records. Verify recall #13207 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #13207) was formally reported on June 5, 2013. It is classified under Moderate severity, with a current status of Active. Ideations DiveAlert, of Seattle, Wash. is listed as the recalling firm. Federal records list the affected scope as About 2,500.
The documented reason for this recall is: The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard. 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 should immediately stop using the recalled DiveAlert signaling devices and return them to an authorized DiveAlert dealer or to DiveAlert for a free repair. The repair consists of replacing … - 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 2,500
Related Recalls
6
3 from same agency
Product description
This recall involves DiveAlert and DiveAlert PLUS scuba dive signaling devices with model numbers DA2, DP2 or DV2. The signaling device is attached to the diver's buoyancy compensator device (BCD) power inflator/alternate regulator system by a chrome-plated brass coupling and is used to activate a loud surface horn or an underwater percussion noise to alert others in the event of a diver's emergency. The devices are also used in non-emergencies to get the attention of the pickup boat or other divers. The DA2 is black with an orange button, the DP2 is black with a gray knob and red button and has DiveAlert PLUS printed on it, and the DV2 is black and red. They can be used with Aqualung AirSource, Oceanic Air XS, Aeris Air Link and Mares Air Control regulator/inflators. Only these signaling devices without any stamped writing on the coupling's collar are included in this recall.
Reason for recall
The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard.
Remedy, what to do
Consumers should immediately stop using the recalled DiveAlert signaling devices and return them to an authorized DiveAlert dealer or to DiveAlert for a free repair. The repair consists of replacing the defective female coupling.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 13207 |
| Date reported | June 5, 2013 |
| Date initiated | June 5, 2013 |
| Recalling firm | Ideations DiveAlert, of Seattle, Wash. |
| Affected scope | About 2,500 |
| 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 DiveAlert signaling devices and return them to an authorized DiveAlert deale…
- Check the recall number (13207) 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? ▼
This recall involves DiveAlert and DiveAlert PLUS scuba dive signaling devices with model numbers DA2, DP2 or DV2. The signaling device is attached to the diver's buoyancy compensator device (BCD) power inflator/alternate regulator system by a chrome-plated brass coupling and is used to activate a loud surface horn or an underwater percussion noise to alert others in the event of a diver's emergency. The devices are also used in non-emergencies to get the attention of the pickup boat or other divers. The DA2 is black with an orange button, the DP2 is black with a gray knob and red button and has DiveAlert PLUS printed on it, and the DV2 is black and red. They can be used with Aqualung AirSource, Oceanic Air XS, Aeris Air Link and Mares Air Control regulator/inflators. Only these signaling devices without any stamped writing on the coupling's collar are included in this recall.. Recalled by Ideations DiveAlert, of Seattle, Wash.. Units affected: About 2,500.
Why was this product recalled? ▼
The signaling device can malfunction when used and restrict the diver's air flow, posing a drowning hazard.
What should consumers do? ▼
Consumers should immediately stop using the recalled DiveAlert signaling devices and return them to an authorized DiveAlert dealer or to DiveAlert for a free repair. The repair consists of replacing the defective female coupling.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 5, 2013. Severity: Moderate. Recall number: 13207.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (13207) 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.
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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 5, 2013. 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.