Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported November 26, 2025
San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
DermaRite Industries, LLC recalled San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 77… - a moderate-severity action.
San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 77… was recalled by DermaRite Industries, LLC in November 26, 2025. Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.. Check the official notice for the remedy. Verify recall #D-0176-2026 with the FDA Drug before acting.
The recall
DermaRite Industries, LLC issued this moderate-severity FDA Drug recall-CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated..
- Moderate
- severity level
- Class II
- classification
- November 26, 2025
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0176-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0176-2026) was formally reported on November 26, 2025, with the manufacturer initiating the action on August 27, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. DermaRite Industries, LLC is listed as the recalling firm, operating out of North Bergen, NJ. Federal records list the affected scope as 15,465 cartridges.
The documented reason for this recall is: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. Distribution data in the federal record shows the product reached: Nationwide 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, 5 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications 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
15,465 cartridges
Related Recalls
6
5 from same agency
Product description
San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34
Reason for recall
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0176-2026 |
| Date reported | November 26, 2025 |
| Date initiated | August 27, 2025 |
| Recalling firm | DermaRite Industries, LLC |
| Firm location | North Bergen, NJ |
| Affected scope | 15,465 cartridges |
| Distribution | Nationwide 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-0176-2026) 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? ▼
San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34. Recalled by DermaRite Industries, LLC. Units affected: 15,465 cartridges.
Why was this product recalled? ▼
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 26, 2025. Severity: Moderate. Recall number: D-0176-2026.
Where was the recalled product distributed? ▼
Distribution: Nationwide in the USA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0176-2026) 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.
FDA Drug Low
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fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3…
IntegraDose Compounding Services LLC · 2026-05-27
FDA Drug Moderate
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
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 November 26, 2025. 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.