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Hemostat
FDA product code HRQ · Class 1 · General, Plastic Surgery
2,348
Registered devices
102
Adverse events
3
Recalls
15
510(k) clearances
Devices with this code
Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMicroFrance® — INTEGRA MICROFRANCEVan Sickle — VAN SICKLE SURGICAL INSTRUMENTS, INCORPORATEDIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSurgical Design — Surgical Design, Inc.ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSurgical Design — Surgical Design, Inc.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftHayden Medical — Hayden Medical, Inc.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftHayden Medical — Hayden Medical, Inc.PRO ADVANTAGE — NATIONAL DISTRIBUTION & CONTRACTING, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAESCULAP — Aesculap AGMillennium — Avalign Technologies, Inc.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-Genossenschaft
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
| 2024-11-12 | MEDLINE INDUSTRIES, LP - Northfield | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
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