PlainRecalls
ModerateClass IITerminated

FDA Drug recall · Reported July 11, 2018

eb5 Skincare that Works. Age Spot Treatment. Skin Lightening Cream with 2% Hydroquinone. 177.4 ml / 6 fl oz carton containing a tube. Manufactured For: EB5 Corporation Portland, OR 97210 Carton Bar Code: 7 41099 00009 9

Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity

Recall #
D-0908-2018
Affected scope
4,632 tubes
Initiated
June 22, 2018
Verify with FDA Drug →
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Eb5 Corporation recalled eb5 Skincare that Works. Age Spot Treatment. Skin Lightening Cream with 2% Hydroquinone. … - a moderate-severity action.

eb5 Skincare that Works. Age Spot Treatment. Skin Lightening Cream with 2% Hydroquinone. … was recalled by Eb5 Corporation in July 11, 2018. Reason: Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity. Check the official notice for the remedy. Verify recall #D-0908-2018 with the FDA Drug before acting.

The recall

Eb5 Corporation issued this moderate-severity FDA Drug recall-Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity.

Moderate
severity level
Class II
classification
July 11, 2018
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0908-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0908-2018) was formally reported on July 11, 2018, with the manufacturer initiating the action on June 22, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Eb5 Corporation is listed as the recalling firm, operating out of Portland, OR. Federal records list the affected scope as 4,632 tubes.

The documented reason for this recall is: Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity Distribution data in the federal record shows the product reached: Distributed Nation Wide in the USA.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - 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.

Cosmetics & Personal Care recalls over time

Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record

-1000100200300400 20052008201120142017202020232026 22
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

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.

Severity

Moderate

Affected scope

4,632 tubes

Related Recalls

6

3 from same agency

Product description

eb5 Skincare that Works. Age Spot Treatment. Skin Lightening Cream with 2% Hydroquinone. 177.4 ml / 6 fl oz carton containing a tube. Manufactured For: EB5 Corporation Portland, OR 97210 Carton Bar Code: 7 41099 00009 9

Reason for recall

Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number D-0908-2018
Date reported July 11, 2018
Date initiated June 22, 2018
Recalling firm Eb5 Corporation
Firm location Portland, OR
Affected scope 4,632 tubes
Distribution Distributed Nation Wide in the USA.

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0908-2018) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug 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?
eb5 Skincare that Works. Age Spot Treatment. Skin Lightening Cream with 2% Hydroquinone. 177.4 ml / 6 fl oz carton containing a tube. Manufactured For: EB5 Corporation Portland, OR 97210 Carton Bar Code: 7 41099 00009 9. Recalled by Eb5 Corporation. Units affected: 4,632 tubes.
Why was this product recalled?
Failed Stability Specifications: Out-of-specification for viscosity, pH and specific gravity
Which agency issued this recall?
This recall was issued by the FDA Drug on July 11, 2018. Severity: Moderate. Recall number: D-0908-2018.
Where was the recalled product distributed?
Distribution: Distributed Nation Wide in the USA..
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0908-2018) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

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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: FDA Drug, reported July 11, 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.