CoValence Laboratories Blemish Spot Treatment 1% Salicylic Acid Recall: Failed Stability
CoValence Laboratories recalls 1% salicylic acid Blemish Spot Treatment bottles due to failed stability specifications. Products may degrade over time, causing potential skin irritation. Check product details and contact for remedy.
Lower-risk recall
Failed Stability Specifications
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What happened, in plain English
CoValence Laboratories is recalling 1% salicylic acid Blemish Spot Treatment bottles that failed stability tests. This could lead to skin irritation or other issues if the product degrades over time. Read more at govinfonow.com/recall/31381-covalence-laboratories-blemish-spot-treatment-1-salicylic-acid-recall-failed.
Source Summary by GovInfoNow · govinfonow.com/recall/31381-covalence-laboratories-blemish-spot-treatment-1-salicylic-acid-recall-failed · Updated August 17, 2026 · FDA enforcement record: FDA #D-0487-2026
Cite this page
“CoValence Laboratories Blemish Spot Treatment 1% Salicylic Acid Recall: Failed Stability.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31381-covalence-laboratories-blemish-spot-treatment-1-salicylic-acid-recall-failed. Based on FDA recall #D-0487-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0487-2026%22&limit=1).
Why it’s dangerous
The product failed stability specifications, meaning it may degrade over time. This could cause skin irritation or other reactions in some users, especially those with sensitive skin.
Who’s affected
People who own or use the recalled Blemish Spot Treatment bottles from Skin Script in Chandler, AZ. Those with sensitive skin may be at higher risk of irritation.
How to tell if you have this one
Check for bottles labeled 'Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml)' from Skin Script in Chandler, AZ. Look for lot numbers 4228D2, 4229D1 (expiring 07/31/2026) or 5147D2 (expiring 04/30/2027).
- Brand
CoValence Laboratories- Product
Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563- Category
Drug
What to do — step by step
Check Product Details
Look for the product name, lot number, and expiration date on the bottle to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “U.S. Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 21 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0487-2026 (April 1, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0487-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.