Severity
Moderate
ModerateActive
CPSC recall · Reported December 3, 2002
CPSC, Oceanic USA Announce Recall of Scuba Regulators
Extreme vibration can occur within these CDX regulators, which can cause an air leakage underwater. Divers could run out of air and drown.
Compiled from official public sources by the editorial team.
Verify with CPSC →
Oceanic USA, of San Leandro, Calif. recalled Oceanic CDX first stage regulators subject to the recall have serial numbers 9200001 to 9… - a moderate-severity action.
CPSC, Oceanic USA Announce Recall of Scuba Regulators was recalled by Oceanic USA, of San Leandro, Calif. in December 3, 2002. Reason: Extreme vibration can occur within these CDX regulators, which can cause an air leakage underwater. Divers co…. Remedy: Consumers should stop using the recalled CDX regulators immediately and take them to any …. Verify recall #03047 with the CPSC before acting.
The recall
Oceanic USA, of San Leandro, Calif. issued this moderate-severity CPSC recall-Extreme vibration can occur within these CDX regulators, which can cause an air leakage underwater. Divers co….
- Moderate
- severity level
- December 3, 2002
- reported
Sourced from official CPSC enforcement records. Verify recall #03047 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #03047) was formally reported on December 3, 2002. It is classified under Moderate severity, with a current status of Active. Oceanic USA, of San Leandro, Calif. is listed as the recalling firm. Federal records list the affected scope as About 24,700.
The documented reason for this recall is: Extreme vibration can occur within these CDX regulators, which can cause an air leakage underwater. Divers could run out of air and drown. 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 recalled CDX regulators immediately and take them to any authorized Oceanic dealer to get a free repair. Other repairs or normal maintenance performed in addition to t… - 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 24,700
Related Recalls
6
6 from same agency
Product description
Oceanic CDX first stage regulators subject to the recall have serial numbers 9200001 to 9205622, 9800013 to 9801711, 0200001 to 0213294, 0D0001 to 0D3046, or 9D0001 to 9D3273. The serial number is stamped into the side of the body of the regulator. The regulators have the name "OCEANIC" written on the rubber boot of the first stage. These CDX regulators were sold with the following second stage regulators: Alpha 7, Delta 3, Gamma 2, and Zeta.
Reason for recall
Extreme vibration can occur within these CDX regulators, which can cause an air leakage underwater. Divers could run out of air and drown.
Remedy, what to do
Consumers should stop using the recalled CDX regulators immediately and take them to any authorized Oceanic dealer to get a free repair. Other repairs or normal maintenance performed in addition to the recall repair will incur a charge.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 03047 |
| Date reported | December 3, 2002 |
| Date initiated | December 3, 2002 |
| Recalling firm | Oceanic USA, of San Leandro, Calif. |
| Affected scope | About 24,700 |
| 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 recalled CDX regulators immediately and take them to any authorized Oceanic dealer to get a free …
- Check the recall number (03047) 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? ▼
Oceanic CDX first stage regulators subject to the recall have serial numbers 9200001 to 9205622, 9800013 to 9801711, 0200001 to 0213294, 0D0001 to 0D3046, or 9D0001 to 9D3273. The serial number is stamped into the side of the body of the regulator. The regulators have the name "OCEANIC" written on the rubber boot of the first stage. These CDX regulators were sold with the following second stage regulators: Alpha 7, Delta 3, Gamma 2, and Zeta.. Recalled by Oceanic USA, of San Leandro, Calif.. Units affected: About 24,700.
Why was this product recalled? ▼
Extreme vibration can occur within these CDX regulators, which can cause an air leakage underwater. Divers could run out of air and drown.
What should consumers do? ▼
Consumers should stop using the recalled CDX regulators immediately and take them to any authorized Oceanic dealer to get a free repair. Other repairs or normal maintenance performed in addition to the recall repair will incur a charge.
Which agency issued this recall? ▼
This recall was issued by the CPSC on December 3, 2002. Severity: Moderate. Recall number: 03047.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (03047) 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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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 December 3, 2002. 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.