Severity
Moderate
ModerateActive
CPSC recall · Reported January 19, 2011
Safety Vacuum Release System Recalled by Vacless Systems Inc. for a Repair/Replace Program to Prevent Entrapment
Improper plastic material found inside the recalled product has been attributed to vacuum release failures which create an entrapment hazard to swimmers and bathers.
Compiled from official public sources by the editorial team.
Verify with CPSC →
Vacless Systems Inc., of Sylmar, Calif. recalled The recalled product is a black plastic device that screws into the drain hole of a swimm… - a moderate-severity action.
Safety Vacuum Release System Recalled by Vacless Systems Inc. for a Repair/Replace Progra… was recalled by Vacless Systems Inc., of Sylmar, Calif. in January 19, 2011. Reason: Improper plastic material found inside the recalled product has been attributed to vacuum release failures wh…. Remedy: Consumers should immediately stop using their pool or spa. Distributors and dealers are d…. Verify recall #11101 with the CPSC before acting.
The recall
Vacless Systems Inc., of Sylmar, Calif. issued this moderate-severity CPSC recall-Improper plastic material found inside the recalled product has been attributed to vacuum release failures wh….
- Moderate
- severity level
- January 19, 2011
- reported
Sourced from official CPSC enforcement records. Verify recall #11101 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #11101) was formally reported on January 19, 2011. It is classified under Moderate severity, with a current status of Active. Vacless Systems Inc., of Sylmar, Calif. is listed as the recalling firm. Federal records list the affected scope as About 1,600.
The documented reason for this recall is: Improper plastic material found inside the recalled product has been attributed to vacuum release failures which create an entrapment hazard to swimmers and bathers. 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 their pool or spa. Distributors and dealers are directly notifying consumers of the recall and the Vacless SVRS repair program. Pool owners/operators who have … - 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 1,600
Related Recalls
6
3 from same agency
Product description
The recalled product is a black plastic device that screws into the drain hole of a swimming pool or spa circulation pump. As part of the circulation systems, the device is designed to release the vacuum in a drain line whenever a submerged drain cover of a swimming pool or spa is completely covered. The recalled product has model number SVRS10ADJ and only involves the following serial numbers found on the weather-proof label attached to the top of every unit: 061040994 through 061041353 071040437 through 071040536 071040570 through 071040574 071040627 through 071041125 081040001 through 081040667
Reason for recall
Improper plastic material found inside the recalled product has been attributed to vacuum release failures which create an entrapment hazard to swimmers and bathers.
Remedy, what to do
Consumers should immediately stop using their pool or spa. Distributors and dealers are directly notifying consumers of the recall and the Vacless SVRS repair program. Pool owners/operators who have not been directly notified should immediately contact Vacless Systems Inc. to implement the Vacless SVRS repair and testing procedure and to receive a replacement unit for installation. The instructions for the repair are also available at www.vacless.com
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 11101 |
| Date reported | January 19, 2011 |
| Date initiated | January 19, 2011 |
| Recalling firm | Vacless Systems Inc., of Sylmar, Calif. |
| Affected scope | About 1,600 |
| 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 their pool or spa. Distributors and dealers are directly notifying consumers of the recal…
- Check the recall number (11101) 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 recalled product is a black plastic device that screws into the drain hole of a swimming pool or spa circulation pump. As part of the circulation systems, the device is designed to release the vacuum in a drain line whenever a submerged drain cover of a swimming pool or spa is completely covered. The recalled product has model number SVRS10ADJ and only involves the following serial numbers found on the weather-proof label attached to the top of every unit: 061040994 through 061041353 071040437 through 071040536 071040570 through 071040574 071040627 through 071041125 081040001 through 081040667. Recalled by Vacless Systems Inc., of Sylmar, Calif.. Units affected: About 1,600.
Why was this product recalled? ▼
Improper plastic material found inside the recalled product has been attributed to vacuum release failures which create an entrapment hazard to swimmers and bathers.
What should consumers do? ▼
Consumers should immediately stop using their pool or spa. Distributors and dealers are directly notifying consumers of the recall and the Vacless SVRS repair program. Pool owners/operators who have not been directly notified should immediately contact Vacless Systems Inc. to implement the Vacless SVRS repair and testing procedure and to receive a replacement unit for installation. The instructions for the repair are also available at www.vacless.com
Which agency issued this recall? ▼
This recall was issued by the CPSC on January 19, 2011. Severity: Moderate. Recall number: 11101.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (11101) 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 19, 2011. 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.