Severity
Moderate
ModerateActive
CPSC recall · Reported June 30, 2010
Aqua Lung America Recalls Apeks WTX Power Inflators Due to Drowning Hazard
The oral inflator button is not properly bonded to the oral stem and can fall off during use, posing a leak of the buoyancy compensator contents. This poses a drowning hazard.
Compiled from official public sources by the editorial team.
Verify with CPSC →
The CPSC recalled The power inflator is the black mouthpiece with the two brass buttons at the end of the c… - a moderate-severity action.
Aqua Lung America Recalls Apeks WTX Power Inflators Due to Drowning Hazard was recalled and listed by the CPSC in June 30, 2010. Reason: The oral inflator button is not properly bonded to the oral stem and can fall off during use, posing a leak o…. Remedy: Consumers should stop diving with their recalled power inflator and bring it or send it t…. Verify recall #10286 with the CPSC before acting.
The recall
issued this moderate-severity CPSC recall-The oral inflator button is not properly bonded to the oral stem and can fall off during use, posing a leak o….
- Moderate
- severity level
- June 30, 2010
- reported
Sourced from official CPSC enforcement records. Verify recall #10286 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #10286) was formally reported on June 30, 2010. 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 1,380 in the U.S., 530 in Canada.
The documented reason for this recall is: The oral inflator button is not properly bonded to the oral stem and can fall off during use, posing a leak of the buoyancy compensator contents. This poses a drowning hazard. 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 diving with their recalled power inflator and bring it or send it to an authorized Apeks dealer. The dealer will apply a free fix. Consumers may also ask for and receive a free … - 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 1,380 in the U.S., 530 in Canada
Related Recalls
6
6 from same agency
Product description
The power inflator is the black mouthpiece with the two brass buttons at the end of the corrugated hose. The recall involves all models of the Apeks WTX power inflators. Some of the recalled components were included on complete air cells. Those model numbers are: 388032, 388060, 388080, 388145, 388260, and 42775. The model number of the air cell can be found on the tag sewn on the center of the air cell or bladder.
Reason for recall
The oral inflator button is not properly bonded to the oral stem and can fall off during use, posing a leak of the buoyancy compensator contents. This poses a drowning hazard.
Remedy, what to do
Consumers should stop diving with their recalled power inflator and bring it or send it to an authorized Apeks dealer. The dealer will apply a free fix. Consumers may also ask for and receive a free replacement product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 10286 |
| Date reported | June 30, 2010 |
| Date initiated | June 30, 2010 |
| Recalling firm | Not disclosed |
| Affected scope | About 1,380 in the U.S., 530 in Canada |
| 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 diving with their recalled power inflator and bring it or send it to an authorized Apeks dealer. The dealer…
- Check the recall number (10286) 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 power inflator is the black mouthpiece with the two brass buttons at the end of the corrugated hose. The recall involves all models of the Apeks WTX power inflators. Some of the recalled components were included on complete air cells. Those model numbers are: 388032, 388060, 388080, 388145, 388260, and 42775. The model number of the air cell can be found on the tag sewn on the center of the air cell or bladder.. Units affected: About 1,380 in the U.S., 530 in Canada.
Why was this product recalled? ▼
The oral inflator button is not properly bonded to the oral stem and can fall off during use, posing a leak of the buoyancy compensator contents. This poses a drowning hazard.
What should consumers do? ▼
Consumers should stop diving with their recalled power inflator and bring it or send it to an authorized Apeks dealer. The dealer will apply a free fix. Consumers may also ask for and receive a free replacement product.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 30, 2010. Severity: Moderate. Recall number: 10286.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (10286) 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.
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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 June 30, 2010. 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.