Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive… — Class II medical device recall Z-1005-2026
Ongoing recall by Ferndale Laboratories, Inc., reported 2026-01-07, distributed nationwide. Butyrate tube cracks during actuation, rendering product unusable.
| Recall number | Z-1005-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ferndale Laboratories, Inc., Ferndale, MI, United States |
| Recall initiated | 2025-11-25 |
| Classified | 2025-12-31 |
| Reported by FDA | 2026-01-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB |
| Quantity | 24,589 |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00304960523488 |
| Lot numbers | 24161BDI |
| Model numbers | 0523-48 |
| Expiration dates | 2029-10-31 |
Product
Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description: Liquid adhesive, 2/3 mL vial, 48 vials per carton Component: No
Reason for recall
Butyrate tube cracks during actuation, rendering product unusable.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1005-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.