Severity
Moderate
ModerateActive
CPSC recall · Reported September 25, 2018
Desert Harvest Recalls Reléveum Skin Repair Cream Due to Failure to Meet Child Resistant Closure Requirements
The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if the contents are swallowed by young children.
Desert Harvest Inc., of Hillsborough, N.c. recalled The recalled Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle w… - a moderate-severity action.
Desert Harvest Recalls Reléveum Skin Repair Cream Due to Failure to Meet Child Resistant … was recalled by Desert Harvest Inc., of Hillsborough, N.c. in September 25, 2018. Reason: The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning ri…. Remedy: Consumers should immediately place the recalled pain relieving cream out of the reach of …. Verify recall #18229 with the CPSC before acting.
The recall
Desert Harvest Inc., of Hillsborough, N.c. issued this moderate-severity CPSC recall-The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning ri….
- Moderate
- severity level
- September 25, 2018
- reported
Sourced from official CPSC enforcement records. Verify recall #18229 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #18229) was formally reported on September 25, 2018. It is classified under Moderate severity, with a current status of Active. Desert Harvest Inc., of Hillsborough, N.c. is listed as the recalling firm. Federal records list the affected scope as About 1,450.
The documented reason for this recall is: The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if the contents are swallowed by young children. 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 place the recalled pain relieving cream out of the reach of children and contact Desert Harvest for a free replacement child resistant cap for the bottle. - 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 1,450
Related Recalls
6
3 from same agency
Product description
The recalled Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle with a white pump dispenser cap and a tan/white gradient label with "Desert Harvest Reléveum" printed on the front. The product is an over the counter skin cream with lidocaine (4%) as the active ingredient. The cream is sold in a 4 ounce or an 8 ounce bottle with the date code "D02N5" printed above the barcode on the bottle.
Reason for recall
The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if the contents are swallowed by young children.
Remedy, what to do
Consumers should immediately place the recalled pain relieving cream out of the reach of children and contact Desert Harvest for a free replacement child resistant cap for the bottle.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 18229 |
| Date reported | September 25, 2018 |
| Date initiated | September 25, 2018 |
| Recalling firm | Desert Harvest Inc., of Hillsborough, N.c. |
| Affected scope | About 1,450 |
| 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 place the recalled pain relieving cream out of the reach of children and contact Desert Harvest for …
- Check the recall number (18229) 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 Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle with a white pump dispenser cap and a tan/white gradient label with "Desert Harvest Reléveum" printed on the front. The product is an over the counter skin cream with lidocaine (4%) as the active ingredient. The cream is sold in a 4 ounce or an 8 ounce bottle with the date code "D02N5" printed above the barcode on the bottle.. Recalled by Desert Harvest Inc., of Hillsborough, N.c.. Units affected: About 1,450.
Why was this product recalled? ▼
The bottles are not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if the contents are swallowed by young children.
What should consumers do? ▼
Consumers should immediately place the recalled pain relieving cream out of the reach of children and contact Desert Harvest for a free replacement child resistant cap for the bottle.
Which agency issued this recall? ▼
This recall was issued by the CPSC on September 25, 2018. Severity: Moderate. Recall number: 18229.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (18229) 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 September 25, 2018. 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.