Severity
Moderate
Vacless Systems Inc., of Sylmar, Calif. issued this CPSC recall on January 19, 2011. Classified as Moderate severity. Approximately About 1,600 units are affected. The recall was issued because: Improper plastic material found inside the recalled product has been attributed to vacuum release failures which create…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
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 indicate About 1,600 units are affected.
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.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 15 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Moderate
Units Affected
About 1,600
Related Recalls
6
0 from same agency
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
Improper plastic material found inside the recalled product has been attributed to vacuum release failures which create an entrapment hazard to swimmers and bathers.
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
| 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. |
| Units affected | About 1,600 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
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Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).