Severity
Moderate
ModerateActive
CPSC recall · Reported September 10, 2008
Aqua Lung Recalls Scuba Regulators and Adapters Due to Drowning Hazard
Over-tightening of the DIN retainer by a technician during installation can result in the retainer breaking under pressure, a rapid escape of air from the scuba cylinder, and the …
Compiled from official public sources by the editorial team.
Verify with CPSC →
Aqua Lung USA, of Vista, Calif. recalled The recalled regulators have a brass DIN retainer manufactured prior to June 2006. The re… - a moderate-severity action.
Aqua Lung Recalls Scuba Regulators and Adapters Due to Drowning Hazard was recalled by Aqua Lung USA, of Vista, Calif. in September 10, 2008. Reason: Over-tightening of the DIN retainer by a technician during installation can result in the retainer breaking u…. Remedy: Consumers should immediately stop using the recalled diving regulators and DIN adaptors a…. Verify recall #08393 with the CPSC before acting.
The recall
Aqua Lung USA, of Vista, Calif. issued this moderate-severity CPSC recall-Over-tightening of the DIN retainer by a technician during installation can result in the retainer breaking u….
- Moderate
- severity level
- September 10, 2008
- reported
Sourced from official CPSC enforcement records. Verify recall #08393 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #08393) was formally reported on September 10, 2008. It is classified under Moderate severity, with a current status of Active. Aqua Lung USA, of Vista, Calif. is listed as the recalling firm. Federal records list the affected scope as About 6,000.
The documented reason for this recall is: Over-tightening of the DIN retainer by a technician during installation can result in the retainer breaking under pressure, a rapid escape of air from the scuba cylinder, and the regulator detaching from the scuba cylin… 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 diving regulators and DIN adaptors and return them to any authorized Aqua Lung dealer for a free replacement DIN retainer. - 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.
Household Products recalls over time
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.
Affected scope
About 6,000
Related Recalls
6
6 from same agency
Product description
The recalled regulators have a brass DIN retainer manufactured prior to June 2006. The recalled Aqua Lung Titan Din 1st Stage regulators have serial numbers lower than 6062501 stamped on the side of the regulator's body. Recalled Titan/Conshelf DIN adaptors are marked "300 BAR MAX" on the side of the part. DIN adaptors marked "300 BAR MAXI" are not included in this recall.
Reason for recall
Over-tightening of the DIN retainer by a technician during installation can result in the retainer breaking under pressure, a rapid escape of air from the scuba cylinder, and the regulator detaching from the scuba cylinder. This poses a drowning hazard to divers.
Remedy, what to do
Consumers should immediately stop using the recalled diving regulators and DIN adaptors and return them to any authorized Aqua Lung dealer for a free replacement DIN retainer.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 08393 |
| Date reported | September 10, 2008 |
| Date initiated | September 10, 2008 |
| Recalling firm | Aqua Lung USA, of Vista, Calif. |
| Affected scope | About 6,000 |
| 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 diving regulators and DIN adaptors and return them to any authorized Aqua Lu…
- Check the recall number (08393) 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 recalled regulators have a brass DIN retainer manufactured prior to June 2006. The recalled Aqua Lung Titan Din 1st Stage regulators have serial numbers lower than 6062501 stamped on the side of the regulator's body. Recalled Titan/Conshelf DIN adaptors are marked "300 BAR MAX" on the side of the part. DIN adaptors marked "300 BAR MAXI" are not included in this recall.. Recalled by Aqua Lung USA, of Vista, Calif.. Units affected: About 6,000.
Why was this product recalled? ▼
Over-tightening of the DIN retainer by a technician during installation can result in the retainer breaking under pressure, a rapid escape of air from the scuba cylinder, and the regulator detaching from the scuba cylinder. This poses a drowning hazard to divers.
What should consumers do? ▼
Consumers should immediately stop using the recalled diving regulators and DIN adaptors and return them to any authorized Aqua Lung dealer for a free replacement DIN retainer.
Which agency issued this recall? ▼
This recall was issued by the CPSC on September 10, 2008. Severity: Moderate. Recall number: 08393.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (08393) 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 September 10, 2008. 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.