Severity
Moderate
CPSC recall · Reported April 17, 2014
The handle grips on each end can break during use and cause parts to be forcefully ejected from the shaft, posing a risk of injury from impact to the user or bystander.
The CPSC recalled This recall involves ISO7X isometric exercise devices. The device is about 3 feet long. I… — a moderate-severity action.
Ontel Recalls Isometric Exercise Devices Due to Projectile Hazard was recalled and listed by the CPSC in April 17, 2014. Reason: The handle grips on each end can break during use and cause parts to be forcefully ejected from the shaft, po…. Remedy: Consumers should immediately stop using the recalled ISO7X isometric exercise device and …. Verify recall #14150 with the CPSC before acting.
The recall
issued this moderate-severity CPSC recall — The handle grips on each end can break during use and cause parts to be forcefully ejected from the shaft, po….
Sourced from official CPSC enforcement records. Verify recall #14150 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This CPSC action (record #14150) was formally reported on April 17, 2014. 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 170,000.
The documented reason for this recall is: The handle grips on each end can break during use and cause parts to be forcefully ejected from the shaft, posing a risk of injury from impact to the user or bystander. 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 the recalled ISO7X isometric exercise device and contact Ontel Products to receive instructions on how to obtain a full refund. — 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 — 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.
Where this recall sits in its category — 40,409 medical devices recalls on record
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 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.
Severity
Moderate
Affected scope
About 170,000
Related Recalls
6
0 from same agency
This recall involves ISO7X isometric exercise devices. The device is about 3 feet long. It has hard plastic black handle grips on each end and two black nylon straps that extend down opposite sides of the center metal shaft. This recall only involves isometric exercise devices with black handle grips.
The handle grips on each end can break during use and cause parts to be forcefully ejected from the shaft, posing a risk of injury from impact to the user or bystander.
Consumers should immediately stop using the recalled ISO7X isometric exercise device and contact Ontel Products to receive instructions on how to obtain a full refund.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 14150 |
| Date reported | April 17, 2014 |
| Date initiated | April 17, 2014 |
| Recalling firm | Not disclosed |
| Affected scope | About 170,000 |
| 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 ISO7X isometric exercise device and contact Ontel Products to receive instru…
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.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported April 17, 2014.
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.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.