PlainRecalls
ModerateClass IIOngoing

FDA Drug recall · Reported July 24, 2024

Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in an HDPE bottle 12 bottles per case, Manufactured By:/Fabrique Par: , Brands International Corp., Newmarket, ON, L3X 2S2, Made in Canada.

Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination

Recall #
D-0598-2024
Affected scope
120,319 bottles
Initiated
June 10, 2024
Verify with FDA Drug →
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Brands International Corporation recalled Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in a… - a moderate-severity action.

Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in a… was recalled by Brands International Corporation in July 24, 2024. Reason: Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination. Check the official notice for the remedy. Verify recall #D-0598-2024 with the FDA Drug before acting.

The recall

Brands International Corporation issued this moderate-severity FDA Drug recall-Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination.

Moderate
severity level
Class II
classification
July 24, 2024
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0598-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0598-2024) was formally reported on July 24, 2024, with the manufacturer initiating the action on June 10, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Brands International Corporation is listed as the recalling firm, operating out of Newmarket. Federal records list the affected scope as 120,319 bottles.

The documented reason for this recall is: Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination Distribution data in the federal record shows the product reached: USA nationwide.. 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 - 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

0100200300400500600 20052008201120142017202020232026 146
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

120,319 bottles

Related Recalls

6

0 from same agency

Product description

Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in an HDPE bottle 12 bottles per case, Manufactured By:/Fabrique Par: , Brands International Corp., Newmarket, ON, L3X 2S2, Made in Canada.

Reason for recall

Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination

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 Ongoing
Recall number D-0598-2024
Date reported July 24, 2024
Date initiated June 10, 2024
Recalling firm Brands International Corporation
Firm location Newmarket
Affected scope 120,319 bottles
Distribution USA nationwide.

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-0598-2024) 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?
Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in an HDPE bottle 12 bottles per case, Manufactured By:/Fabrique Par: , Brands International Corp., Newmarket, ON, L3X 2S2, Made in Canada.. Recalled by Brands International Corporation. Units affected: 120,319 bottles.
Why was this product recalled?
Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination
Which agency issued this recall?
This recall was issued by the FDA Drug on July 24, 2024. Severity: Moderate. Recall number: D-0598-2024.
Where was the recalled product distributed?
Distribution: USA nationwide..
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0598-2024) 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

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: FDA Drug, reported July 24, 2024. 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.