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HU-FRIEDY MFG. CO., LLC · Model CS324 · UDI-DI 10889950007232

GAF
5
510(k) clearances
10
Adverse events
1
Recalls
205
Facilities

Description

#324 Rigid Cement Spatula

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.