Severity
Moderate
ModerateActive
CPSC recall · Reported June 22, 2006
Oceanic Recalls Digital Dive Computer Due to Decompression Hazard
When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed can exceed the actual elapsed time under water. This can cause divers to…
Compiled from official public sources by the editorial team.
Verify with CPSC →
Oceanic, of San Leandro, Calif. recalled The recall involves Oceanic-brand Versa Pro 2A dive computers with serial numbers 12000 t… - a moderate-severity action.
Oceanic Recalls Digital Dive Computer Due to Decompression Hazard was recalled by Oceanic, of San Leandro, Calif. in June 22, 2006. Reason: When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed ca…. Remedy: Consumers should discard this recalled product. The remedy is no longer available.. Verify recall #06194 with the CPSC before acting.
The recall
Oceanic, of San Leandro, Calif. issued this moderate-severity CPSC recall-When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed ca….
- Moderate
- severity level
- June 22, 2006
- reported
Sourced from official CPSC enforcement records. Verify recall #06194 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #06194) was formally reported on June 22, 2006. It is classified under Moderate severity, with a current status of Active. Oceanic, of San Leandro, Calif. is listed as the recalling firm. Federal records list the affected scope as About 6,100.
The documented reason for this recall is: When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed can exceed the actual elapsed time under water. This can cause divers to ascend before fulfilling a decompressio… 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 discard this recalled product. The remedy is no longer available. - 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.
Electronics recalls over time
Where this recall sits in its category - 609 electronics 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 6,100
Related Recalls
6
6 from same agency
Product description
The recall involves Oceanic-brand Versa Pro 2A dive computers with serial numbers 12000 through 18176, which can be accessed and viewed on the computer's display. The serial number and "r2A" are printed on the side of the unit. This recall does not include any other Oceanic brand dive computer, or Versa Pro 2A while operated in normal decompression dive computer mode.
Reason for recall
When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed can exceed the actual elapsed time under water. This can cause divers to ascend before fulfilling a decompression obligation, resulting in decompression sickness.
Remedy, what to do
Consumers should discard this recalled product. The remedy is no longer available.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 06194 |
| Date reported | June 22, 2006 |
| Date initiated | June 22, 2006 |
| Recalling firm | Oceanic, of San Leandro, Calif. |
| Affected scope | About 6,100 |
| 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 discard this recalled product. The remedy is no longer available.
- Check the recall number (06194) 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 Oceanic-brand Versa Pro 2A dive computers with serial numbers 12000 through 18176, which can be accessed and viewed on the computer's display. The serial number and "r2A" are printed on the side of the unit. This recall does not include any other Oceanic brand dive computer, or Versa Pro 2A while operated in normal decompression dive computer mode.. Recalled by Oceanic, of San Leandro, Calif.. Units affected: About 6,100.
Why was this product recalled? ▼
When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed can exceed the actual elapsed time under water. This can cause divers to ascend before fulfilling a decompression obligation, resulting in decompression sickness.
What should consumers do? ▼
Consumers should discard this recalled product. The remedy is no longer available.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 22, 2006. Severity: Moderate. Recall number: 06194.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (06194) 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.
CPSC Moderate
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CPSC Moderate
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School Specialty, LLC, of Greenville, Wisconsin · 2026-06-11
Compare this recall with Projecting LED Finger Light Toys Recalled Due to Risk of Se… →
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 22, 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.