PlainRecalls
CriticalClass ITerminated

FDA Drug recall · Reported November 24, 2021

LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3

Chemical Contamination: presence of benzene

Recall #
D-0246-2022
Affected scope
2,817,468 cans
Initiated
October 1, 2021
Verify with FDA Drug →
View my saved recalls

Bayer Healthcare Pharmaceuticals Inc. recalled LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dis… - a critical-severity action.

LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dis… was recalled by Bayer Healthcare Pharmaceuticals Inc. in November 24, 2021. Reason: Chemical Contamination: presence of benzene. Check the official notice for the remedy. Verify recall #D-0246-2022 with the FDA Drug before acting.

The recall

Bayer Healthcare Pharmaceuticals Inc. issued this critical-severity FDA Drug recall-Chemical Contamination: presence of benzene.

Critical
severity level
Class I
classification
November 24, 2021
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0246-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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 - 1,371 cosmetics & personal care recalls on record

0100200300400 20052008201120142017202020232026 33
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3

Reason for recall

Chemical Contamination: presence of benzene

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number D-0246-2022
Date reported November 24, 2021
Date initiated October 1, 2021
Recalling firm Bayer Healthcare Pharmaceuticals Inc.
Firm location Whippany, NJ
Affected scope 2,817,468 cans
Distribution Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.

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-0246-2022) 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.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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?
LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3. Recalled by Bayer Healthcare Pharmaceuticals Inc.. Units affected: 2,817,468 cans.
Why was this product recalled?
Chemical Contamination: presence of benzene
Which agency issued this recall?
This recall was issued by the FDA Drug on November 24, 2021. Severity: Critical. Recall number: D-0246-2022.
Where was the recalled product distributed?
Distribution: Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels..
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.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Similar Cosmetics & Personal Care · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Compare this recall with Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 7… → · All Cosmetics & Personal Care recalls

This recall: FDA Drug, reported November 24, 2021. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026