Severity
Moderate
ModerateActive
CPSC recall · Reported July 21, 2022
Aqualung Recalls i330R SCUBA Diving Computers Due to Injury and Drowning Hazards
The recalled diving computers can fail to adjust to the user's altitude and display incorrect calculations for sea level dive times at altitudes exceeding 3,000 feet, posing injur…
The CPSC recalled This recall involves Aqualung i330R SCUBA Diving Computers. The wrist device is black and… - a moderate-severity action.
Aqualung Recalls i330R SCUBA Diving Computers Due to Injury and Drowning Hazards was recalled and listed by the CPSC in July 21, 2022. Reason: The recalled diving computers can fail to adjust to the user's altitude and display incorrect calculations fo…. Remedy: Consumers should immediately stop using the recalled Aqualung i330R SCUBA Diving Computer…. Verify recall #22187 with the CPSC before acting.
The recall
issued this moderate-severity CPSC recall-The recalled diving computers can fail to adjust to the user's altitude and display incorrect calculations fo….
- Moderate
- severity level
- July 21, 2022
- reported
Sourced from official CPSC enforcement records. Verify recall #22187 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #22187) was formally reported on July 21, 2022. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records list the affected scope as About 16,400.
The documented reason for this recall is: The recalled diving computers can fail to adjust to the user's altitude and display incorrect calculations for sea level dive times at altitudes exceeding 3,000 feet, posing injury (decompression sickness) and drowning … 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 Aqualung i330R SCUBA Diving Computers and contact Aqua Lung to arrange for a free repair. Consumers can download a software update through the Div… - 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, 3 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.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices 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 16,400
Related Recalls
6
3 from same agency
Product description
This recall involves Aqualung i330R SCUBA Diving Computers. The wrist device is black and has a bright color display and two-button interface. "AQUA LUNG" is printed on the front and back of each device. The model number is printed on the back of the device. The serial number is printed on a label located on the back of the device. Both the model and serial numbers can also be found by scrolling through the diving computer. Model numbers, serial number ranges and manufactured dates are as follows: Model number Serial number range Manufactured dates Units affected Black/NS159000 GD-001004 to GD-015302 February 2021 and February 2022 14000 2-GAUGE, PSI (Console) /NS159001 GM-001000 to GM-003305 December 2021 and February 2022 2200 2-GAUGE, BAR/NS159002 (Console), GM-001011 to GM-001269 December 2021 and February 2022 129
Reason for recall
The recalled diving computers can fail to adjust to the user's altitude and display incorrect calculations for sea level dive times at altitudes exceeding 3,000 feet, posing injury (decompression sickness) and drowning hazards.
Remedy, what to do
Consumers should immediately stop using the recalled Aqualung i330R SCUBA Diving Computers and contact Aqua Lung to arrange for a free repair. Consumers can download a software update through the DiverLog+ application or bring their recalled dive computer to their dealer or local dive center to have the software update installed.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 22187 |
| Date reported | July 21, 2022 |
| Date initiated | July 21, 2022 |
| Recalling firm | Not disclosed |
| Affected scope | About 16,400 |
| 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 Aqualung i330R SCUBA Diving Computers and contact Aqua Lung to arrange for a…
- Check the recall number (22187) 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? ▼
This recall involves Aqualung i330R SCUBA Diving Computers. The wrist device is black and has a bright color display and two-button interface. "AQUA LUNG" is printed on the front and back of each device. The model number is printed on the back of the device. The serial number is printed on a label located on the back of the device. Both the model and serial numbers can also be found by scrolling through the diving computer. Model numbers, serial number ranges and manufactured dates are as follows: Model number Serial number range Manufactured dates Units affected Black/NS159000 GD-001004 to GD-015302 February 2021 and February 2022 14000 2-GAUGE, PSI (Console) /NS159001 GM-001000 to GM-003305 December 2021 and February 2022 2200 2-GAUGE, BAR/NS159002 (Console), GM-001011 to GM-001269 December 2021 and February 2022 129. Units affected: About 16,400.
Why was this product recalled? ▼
The recalled diving computers can fail to adjust to the user's altitude and display incorrect calculations for sea level dive times at altitudes exceeding 3,000 feet, posing injury (decompression sickness) and drowning hazards.
What should consumers do? ▼
Consumers should immediately stop using the recalled Aqualung i330R SCUBA Diving Computers and contact Aqua Lung to arrange for a free repair. Consumers can download a software update through the DiverLog+ application or bring their recalled dive computer to their dealer or local dive center to have the software update installed.
Which agency issued this recall? ▼
This recall was issued by the CPSC on July 21, 2022. Severity: Moderate. Recall number: 22187.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (22187) 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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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 July 21, 2022. 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.