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…

Recall #: 06194
Affected scope: About 6,100

Compiled from official public sources by the publisher. · Updated September 2026

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Oceanic, of San Leandro, Calif. recalled The recall involves Oceanic-brand Versa Pro 2A dive computers with serial numbers 12000 t….

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 CPSC recall-When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed ca….

None
agency class: 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 recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. Consumers holding this product should act on the agency's documented remedy above 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.

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

Structured summary of the CPSC recall record
Attribute	Value
Agency	U.S. Consumer Product Safety Commission
Severity class	Not classified by agency
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? ▼

Why was this product recalled? ▼

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. CPSC does not publish a hazard classification for this recall. Recall number: 06194.

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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Similar severity · nearest report date

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This recall: CPSC, reported June 22, 2006. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026