Severity
Moderate
ModerateActive
CPSC recall · Reported January 25, 2007
Flojet Recalls VAC Pumps Sold With LeBleu 50-Gallon Bottled Water System for Shock Hazard
A manufacturing defect can cause consumers to receive an electric shock when the metal housing is touched.
Compiled from official public sources by the editorial team.
Verify with CPSC →
Flojet Division of Itt Corp., of Santa Ana, Calif. recalled The recall involves Duplex II 115 VAC Pumps sold as a component of the LeBleu Automatic 5… - a moderate-severity action.
Flojet Recalls VAC Pumps Sold With LeBleu 50-Gallon Bottled Water System for Shock Hazard was recalled by Flojet Division of Itt Corp., of Santa Ana, Calif. in January 25, 2007. Reason: A manufacturing defect can cause consumers to receive an electric shock when the metal housing is touched.. Remedy: A representative of the LeBleu Corp. or a trained licensee will inspect all installed pum…. Verify recall #07524 with the CPSC before acting.
The recall
Flojet Division of Itt Corp., of Santa Ana, Calif. issued this moderate-severity CPSC recall-A manufacturing defect can cause consumers to receive an electric shock when the metal housing is touched..
- Moderate
- severity level
- January 25, 2007
- reported
Sourced from official CPSC enforcement records. Verify recall #07524 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #07524) was formally reported on January 25, 2007. It is classified under Moderate severity, with a current status of Active. Flojet Division of Itt Corp., of Santa Ana, Calif. is listed as the recalling firm. Federal records list the affected scope as About 500.
The documented reason for this recall is: A manufacturing defect can cause consumers to receive an electric shock when the metal housing is touched. 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: A representative of the LeBleu Corp. or a trained licensee will inspect all installed pumps to determine if the defect is present, and, if so, the pump will be replaced. All products installed in new… - 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 500
Related Recalls
6
3 from same agency
Product description
The recall involves Duplex II 115 VAC Pumps sold as a component of the LeBleu Automatic 50-Gallon Bottled Water System. Model numbers included in this recall are D08X000A and D08X000B. A silver Flojet label that includes the model number is affixed to the front of the pump. The pumps are installed exclusively in 50-gallon bottled water that were sold, installed and maintained by LeBleu Corp. or its licensees.
Reason for recall
A manufacturing defect can cause consumers to receive an electric shock when the metal housing is touched.
Remedy, what to do
A representative of the LeBleu Corp. or a trained licensee will inspect all installed pumps to determine if the defect is present, and, if so, the pump will be replaced. All products installed in new home construction, which have not yet been started up, will be removed and replaced.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 07524 |
| Date reported | January 25, 2007 |
| Date initiated | January 25, 2007 |
| Recalling firm | Flojet Division of Itt Corp., of Santa Ana, Calif. |
| Affected scope | About 500 |
| 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
A representative of the LeBleu Corp. or a trained licensee will inspect all installed pumps to determine if the defect is present…
- Check the recall number (07524) 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 recall involves Duplex II 115 VAC Pumps sold as a component of the LeBleu Automatic 50-Gallon Bottled Water System. Model numbers included in this recall are D08X000A and D08X000B. A silver Flojet label that includes the model number is affixed to the front of the pump. The pumps are installed exclusively in 50-gallon bottled water that were sold, installed and maintained by LeBleu Corp. or its licensees.. Recalled by Flojet Division of Itt Corp., of Santa Ana, Calif.. Units affected: About 500.
Why was this product recalled? ▼
A manufacturing defect can cause consumers to receive an electric shock when the metal housing is touched.
What should consumers do? ▼
A representative of the LeBleu Corp. or a trained licensee will inspect all installed pumps to determine if the defect is present, and, if so, the pump will be replaced. All products installed in new home construction, which have not yet been started up, will be removed and replaced.
Which agency issued this recall? ▼
This recall was issued by the CPSC on January 25, 2007. Severity: Moderate. Recall number: 07524.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (07524) 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 January 25, 2007. 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.