Severity
Moderate
ModerateActive
CPSC recall · Reported May 27, 2020
Sanvall Enterprises Recalls Rapid Alivio Pain Relieving Roll-On Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the pro…
Sanvall Enterprises Inc., of Doral, Fla. recalled This recall involves Sanvall Rapid Alivio Pain Relieving Roll-On in a 3 fl. oz (88.5 mL) … - a moderate-severity action.
Sanvall Enterprises Recalls Rapid Alivio Pain Relieving Roll-On Due to Failure to Meet Ch… was recalled by Sanvall Enterprises Inc., of Doral, Fla. in May 27, 2020. Reason: The product contains the substance methyl salicylate which must be in child resistant packaging as required b…. Remedy: Consumers should immediately store the pain relieving roll-on in a safe location out of r…. Verify recall #20126 with the CPSC before acting.
The recall
Sanvall Enterprises Inc., of Doral, Fla. issued this moderate-severity CPSC recall-The product contains the substance methyl salicylate which must be in child resistant packaging as required b….
- Moderate
- severity level
- 5K units
- affected scope
- May 27, 2020
- reported
Sourced from official CPSC enforcement records. Verify recall #20126 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #20126) was formally reported on May 27, 2020. It is classified under Moderate severity, with a current status of Active. Sanvall Enterprises Inc., of Doral, Fla. is listed as the recalling firm. Federal records list the affected scope as 5400.
The documented reason for this recall is: The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a ri… 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 store the pain relieving roll-on in a safe location out of reach of children and contact Sanvall Enterprises for 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, 6 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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
5400
Related Recalls
6
6 from same agency
Product description
This recall involves Sanvall Rapid Alivio Pain Relieving Roll-On in a 3 fl. oz (88.5 mL) white plastic bottle with a white cap and a red, white and blue label. "Rapid Alivio," "Maximum Strength Pain Relieving Liquid" and "Para Dolor Muscular" are printed on the label. Lot numbers 18032201, 18032301, 19040501, or 19052801 are printed on the bottom of the bottle. UPC code 605100014225 is printed on the side of the label.
Reason for recall
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
Remedy, what to do
Consumers should immediately store the pain relieving roll-on in a safe location out of reach of children and contact Sanvall Enterprises for a full refund.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 20126 |
| Date reported | May 27, 2020 |
| Date initiated | May 27, 2020 |
| Recalling firm | Sanvall Enterprises Inc., of Doral, Fla. |
| Affected scope | 5400 |
| 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 store the pain relieving roll-on in a safe location out of reach of children and contact Sanvall Ent…
- Check the recall number (20126) 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? ▼
This recall involves Sanvall Rapid Alivio Pain Relieving Roll-On in a 3 fl. oz (88.5 mL) white plastic bottle with a white cap and a red, white and blue label. "Rapid Alivio," "Maximum Strength Pain Relieving Liquid" and "Para Dolor Muscular" are printed on the label. Lot numbers 18032201, 18032301, 19040501, or 19052801 are printed on the bottom of the bottle. UPC code 605100014225 is printed on the side of the label.. Recalled by Sanvall Enterprises Inc., of Doral, Fla.. Units affected: 5400.
Why was this product recalled? ▼
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
What should consumers do? ▼
Consumers should immediately store the pain relieving roll-on in a safe location out of reach of children and contact Sanvall Enterprises for a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on May 27, 2020. Severity: Moderate. Recall number: 20126.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (20126) 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.
CPSC Moderate
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Compare this recall with AMASKY Nursing Pillows Recalled Due to Risk of Serious Inju… →
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 May 27, 2020. 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.