PlainRecalls

Oceanic Recalls Digital Dive Computer Due to Decompression Hazard

Reported: June 22, 2006 Initiated: June 22, 2006 #06194 About 6,100 units

Oceanic, of San Leandro, Calif. issued this CPSC recall on June 22, 2006. Classified as Moderate severity. Approximately About 6,100 units are affected. The recall was issued because: When using the dive computer set for "User Selected Digital Gauge Mode," the "Elapsed Dive Time" displayed can exceed t…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

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 indicate About 6,100 units are affected.

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.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 20 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

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

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 Moderate
Status Active
Recall number 06194
Date reported June 22, 2006
Date initiated June 22, 2006
Recalling firm Oceanic, of San Leandro, Calif.
Units affected About 6,100
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 6,100 units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

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.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

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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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).