Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported June 20, 2018
Acne Shave 3 Step Shaving System, contains one tube Acne Shave (salicylic acid) Shave Cream Acne Shield, one tube Acne Shave Post-Shave Moisturizer (salicylic acid), 0.5% tube, and one Power Shaver per box, Distributed by: United Exchange Corp., 17311 Valley View Blvd, Cerritos CA 90703 USA, UPC 7 80707 73114 7.
CGMP Deviations: products may be contaminated with bacteria.
Shadow Holdings DBA Bocchi Labs recalled Acne Shave 3 Step Shaving System, contains one tube Acne Shave (salicylic acid) Shave Cre… - a moderate-severity action.
Acne Shave 3 Step Shaving System, contains one tube Acne Shave (salicylic acid) Shave Cre… was recalled by Shadow Holdings DBA Bocchi Labs in June 20, 2018. Reason: CGMP Deviations: products may be contaminated with bacteria.. Check the official notice for the remedy. Verify recall #D-0861-2018 with the FDA Drug before acting.
The recall
Shadow Holdings DBA Bocchi Labs issued this moderate-severity FDA Drug recall-CGMP Deviations: products may be contaminated with bacteria..
- Moderate
- severity level
- Class II
- classification
- June 20, 2018
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0861-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0861-2018) was formally reported on June 20, 2018, with the manufacturer initiating the action on May 25, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Shadow Holdings DBA Bocchi Labs is listed as the recalling firm, operating out of Santa Clarita, CA. Federal records list the affected scope as 4,932 boxes.
The documented reason for this recall is: CGMP Deviations: products may be contaminated with bacteria. 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, 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
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
4,932 boxes
Related Recalls
6
3 from same agency
Product description
Acne Shave 3 Step Shaving System, contains one tube Acne Shave (salicylic acid) Shave Cream Acne Shield, one tube Acne Shave Post-Shave Moisturizer (salicylic acid), 0.5% tube, and one Power Shaver per box, Distributed by: United Exchange Corp., 17311 Valley View Blvd, Cerritos CA 90703 USA, UPC 7 80707 73114 7.
Reason for recall
CGMP Deviations: products may be contaminated with bacteria.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0861-2018 |
| Date reported | June 20, 2018 |
| Date initiated | May 25, 2018 |
| Recalling firm | Shadow Holdings DBA Bocchi Labs |
| Firm location | Santa Clarita, CA |
| Affected scope | 4,932 boxes |
| 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-0861-2018) 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? ▼
Acne Shave 3 Step Shaving System, contains one tube Acne Shave (salicylic acid) Shave Cream Acne Shield, one tube Acne Shave Post-Shave Moisturizer (salicylic acid), 0.5% tube, and one Power Shaver per box, Distributed by: United Exchange Corp., 17311 Valley View Blvd, Cerritos CA 90703 USA, UPC 7 80707 73114 7.. Recalled by Shadow Holdings DBA Bocchi Labs. Units affected: 4,932 boxes.
Why was this product recalled? ▼
CGMP Deviations: products may be contaminated with bacteria.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 20, 2018. Severity: Moderate. Recall number: D-0861-2018.
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-0861-2018) 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
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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PS Seasoning & Spices, Inc. · 2026-05-27
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MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Pha…
Wisconsin Pharmacal Company · 2026-05-27
FDA Drug Moderate
Fluocinonide, USP, 0.05% Cream, 30g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1…
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Compare this recall with Tiny Land Children's Play Tents Recalled Due to Risk of Inj… →
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 June 20, 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.