Tissue-Tek PARAFORM PROC/EMB/MEDIUM — Class II medical device recall Z-1748-2014
Terminated recall by Sakura Finetek USA Inc, reported 2014-06-18, distributed nationwide. This Lot has variations in melting temperature.
| Recall number | Z-1748-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sakura Finetek USA Inc, Torrance, CA, United States |
| Recall initiated | 2014-04-16 |
| Classified | 2014-06-10 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2014-09-02 |
| Distributed | Nationwide (US) |
| Quantity | 115 |
| Lot numbers | 263922 |
Product
Tissue-Tek PARAFORM PROC/EMB/MEDIUM, FORMULA 3 - 8x1Kg. for diagnostic chemistry use. Sakura Finetek USA, Inc.
Reason for recall
This Lot has variations in melting temperature.
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-1748-2014. 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.