PlainRecalls

Euqee Wintergreen Essential Oils Recalled Due to Risk of Poisoning; Violation of the Poison Prevention Packaging Act; Sold Exclusively on Amazon.com by DLWL-US

Reported: January 2, 2025 Initiated: January 2, 2025 #25081 About 3,750 units

The recall

DingLinWangLuoKeJiGuang ZhouYouXianGongSi, dba Dlwl-us, of China issued this moderate-severity CPSC recall — The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the ….

Moderate
severity level
About 3,750
units affected
January 2, 2025
reported

Sourced from official CPSC enforcement records. Verify recall #25081 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This CPSC action (record #25081) was formally reported on January 2, 2025. It is classified under Moderate severity, with a current status of Active. DingLinWangLuoKeJiGuang ZhouYouXianGongSi, dba Dlwl-us, of China is listed as the recalling firm. Federal records indicate About 3,750 units are affected.

The documented reason for this recall is: The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the products is not child-resistant, posing a risk o… 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 secure the recalled essential oil out of the sight and reach of children and contact DLWL-US for a full refund. Consumers can request a pre-paid label and free packaging … — 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 and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by CPSC. 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 1 year 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.

Where this recall sits in the database

Severity2119858883High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.

Severity

Moderate

Units Affected

About 3,750

Related Recalls

6

6 from same agency

Product Description

This recall involves Euqee Wintergreen Essential Oil Bottles. The oil was sold in amber glass bottles with a black screw-on cap in the size of 118 ml. "Euqee, Essential Oil, Premium Grade, 100% Pure Plant Extract and Wintergreen" is printed on a white label on the front of the bottle. The back label contains safety disclosures, storage instructions and manufacturer information.

Reason for Recall

The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.

Remedy

Consumers should immediately secure the recalled essential oil out of the sight and reach of children and contact DLWL-US for a full refund. Consumers can request a pre-paid label and free packaging to return the Euqee Wintergreen Essential Oil. DLWL-US and Amazon.com are contacting all known purchasers directly.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 25081
Date reported January 2, 2025
Date initiated January 2, 2025
Recalling firm DingLinWangLuoKeJiGuang ZhouYouXianGongSi, dba Dlwl-us, of China
Units affected About 3,750
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 3,750 units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
This recall involves Euqee Wintergreen Essential Oil Bottles. The oil was sold in amber glass bottles with a black screw-on cap in the size of 118 ml. "Euqee, Essential Oil, Premium Grade, 100% Pure Plant Extract and Wintergreen" is printed on a white label on the front of the bottle. The back label contains safety disclosures, storage instructions and manufacturer information.. Recalled by DingLinWangLuoKeJiGuang ZhouYouXianGongSi, dba Dlwl-us, of China. Units affected: About 3,750.
Why was this product recalled?
The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
What should consumers do?
Consumers should immediately secure the recalled essential oil out of the sight and reach of children and contact DLWL-US for a full refund. Consumers can request a pre-paid label and free packaging to return the Euqee Wintergreen Essential Oil. DLWL-US and Amazon.com are contacting all known purchasers directly.
Which agency issued this recall?
This recall was issued by the CPSC on January 2, 2025. Severity: Moderate. Recall number: 25081.
How do I check if my product is affected by a recall?
Check the product description and recall number (25081) 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.

Recall Context

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.

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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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: CPSC, reported January 2, 2025.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

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.

Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).