Severity
Moderate
CPSC recall · Reported June 7, 2006
A manufacturing error could cause the main housing of some regulators to change shape over time, which could cause the cover and diaphragm to become dislodged. If this occurs, air…
Scubapro® with global headquarters located in El Cajon, Calif. recalled The recall involves some X650 second stage regulators. All X650 second stage regulators a… - a moderate-severity action.
Scubapro® X650 Diving Regulators Recalled for Drowning Hazard was recalled by Scubapro® with global headquarters located in El Cajon, Calif. in June 7, 2006. Reason: A manufacturing error could cause the main housing of some regulators to change shape over time, which could …. Remedy: Consumers should stop using the product immediately and contact Scubapro® to determine if…. Verify recall #06177 with the CPSC before acting.
The recall
Scubapro® with global headquarters located in El Cajon, Calif. issued this moderate-severity CPSC recall-A manufacturing error could cause the main housing of some regulators to change shape over time, which could ….
Sourced from official CPSC enforcement records. Verify recall #06177 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This CPSC action (record #06177) was formally reported on June 7, 2006. It is classified under Moderate severity, with a current status of Active. Scubapro® with global headquarters located in El Cajon, Calif. is listed as the recalling firm. Federal records list the affected scope as About 670.
The documented reason for this recall is: A manufacturing error could cause the main housing of some regulators to change shape over time, which could cause the cover and diaphragm to become dislodged. If this occurs, air flow will be interrupted and the regula… 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 stop using the product immediately and contact Scubapro® to determine if they have an affected second stage regulator. If so, they will receive a free replacement regulator. The comp… - 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, 6 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.
Where this recall sits in its category - 3,056 household products 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.
Severity
Moderate
Affected scope
About 670
Related Recalls
6
6 from same agency
The recall involves some X650 second stage regulators. All X650 second stage regulators are clearly marked with a blue capital "X" next to the numbers "650" in white. Affected regulators have a visible bump located on the right side of the unit between the letter "C" and where the mouthpiece attaches to the regulator body.
A manufacturing error could cause the main housing of some regulators to change shape over time, which could cause the cover and diaphragm to become dislodged. If this occurs, air flow will be interrupted and the regulators will no longer function, posing a drowning hazard to users.
Consumers should stop using the product immediately and contact Scubapro® to determine if they have an affected second stage regulator. If so, they will receive a free replacement regulator. The company is contacting registered owners of the product directly.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 06177 |
| Date reported | June 7, 2006 |
| Date initiated | June 7, 2006 |
| Recalling firm | Scubapro® with global headquarters located in El Cajon, Calif. |
| Affected scope | About 670 |
| 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 stop using the product immediately and contact Scubapro® to determine if they have an affected second stage regu…
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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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 7, 2006. 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.