CPSC recall · Reported September 12, 2024
About 866,000 AirJet and HydroJet Spa Pumps Recalled Due to Fire Hazard; One Death Reported; Manufactured by Bestway and Sold with SaluSpa, Coleman, and Hydro-Force Spa Liners
The recalled AirJet and HydroJet spa pumps can overheat causing the plastic housing to ignite, posing a fire hazard.
Bestway (Hong Kong) International Ltd., of China recalled The spa pumps could have been sold separately, or in a package with an inflatable spa lin….
About 866,000 AirJet and HydroJet Spa Pumps Recalled Due to Fire Hazard; One Death Report… was recalled by Bestway (Hong Kong) International Ltd., of China in September 12, 2024. Reason: The recalled AirJet and HydroJet spa pumps can overheat causing the plastic housing to ignite, posing a fire …. Remedy: Consumers should immediately stop using the recalled spa pumps, and contact Bestway to re…. Verify recall #24359 with the CPSC before acting.
The recall
Bestway (Hong Kong) International Ltd., of China issued this CPSC recall-The recalled AirJet and HydroJet spa pumps can overheat causing the plastic housing to ignite, posing a fire ….
- None
- agency class
- September 12, 2024
- reported
Sourced from official CPSC enforcement records. Verify recall #24359 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 - 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 - 41,021 medical devices recalls on record
Product description
The spa pumps could have been sold separately, or in a package with an inflatable spa liner in different colors, styles, and inflatable spa sizes. The inflatable spa liners packaged with the pumps are sold under the brand names SaluSpa, Coleman, and Hydro-Force, which are printed on the side of the liner. This recall only includes AirJet and HydroJet Spa Pump model numbers P05332, P05339, P05711, P05807, P07000, P07001, P05511, P07034, and P07572. "Bestway" and the model number are printed on the label on the side or back of the spa pump.
Reason for recall
The recalled AirJet and HydroJet spa pumps can overheat causing the plastic housing to ignite, posing a fire hazard.
Remedy, what to do
Consumers should immediately stop using the recalled spa pumps, and contact Bestway to receive a free replacement spa pump or a refund of $100 for AirJet spa pumps, or $189 for HydroJet spa pumps.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Not classified by agency |
| Status | Active |
| Recall number | 24359 |
| Date reported | September 12, 2024 |
| Date initiated | September 12, 2024 |
| Recalling firm | Bestway (Hong Kong) International Ltd., of China |
| Affected scope | About 866,000 |
| 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 spa pumps, and contact Bestway to receive a free replacement spa pump or a r…
- Check the recall number (24359) 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? ▼
Which agency issued this recall? ▼
How do I report an injury from a recalled product? ▼
Nationwide recalls with similar severity or category timing
Consumer-product notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade, closest by report date among other firms and states.
Similar Medical Devices · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Compare this recall with GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VS… → · All Medical Devices recalls
Methodology · Corrections · Archive as of August 2026