Ferndale Laboratories recalls Mastisol Liquid Adhesive (model 0523-48) due to butyrate tube cracking during actuation, rendering product unusable. Affected units sold from 2023-2029.
Butyrate tube cracks during actuation, rendering product unusable.
Ferndale Laboratories is recalling Mastisol Liquid Adhesive (model 0523-48) because the butyrate tube cracks during use, making the product unusable. This issue affects users who rely on the adhesive for medical applications.
The butyrate tube cracks during actuation, which means the adhesive becomes unusable. This could lead to improper medical application if the product is still used after cracking.
Users of Mastisol Liquid Adhesive for medical applications are affected. Those who have the specific model (0523-48) and are using it for medical purposes are most at risk.
Check for the model number 0523-48 on the vial. The product is a liquid adhesive in 2/3 mL vials, 48 per carton, with expiration date 10/31/2029.
Verify the model number on the vial (0523-48) and expiration date (10/31/2029).
The butyrate tube cracks during actuation, rendering the product unusable.
The recall record does not specify a remedy, so check product details and contact the manufacturer if needed.
The product was sold from 2023 to 2029 based on the expiration date.
We’ve drafted a message you can send Mastisol to request your refund or repair — edit it as you like.
Subject: Recall Z-1005-2026 — Mastisol Mastisol Hello, I own a Mastisol that is covered by recall Z-1005-2026 from Mastisol. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
