Home › Device types › KMF
Bandage, Liquid
FDA product code KMF · Class 1 · General Hospital
205
Registered devices
276
Adverse events
4
Recalls
222
510(k) clearances
Devices with this code
Curity — Cardinal Health 200, LLCGluSeal® — Glustich IncKendall — Cardinal Health, Inc.ElaSkin — ALEO BME, INC.PolyMem — FERRIS MFG. CORP.Natural Seal Wound Dressing 1oz — Kericure Inc.PolyMem — FERRIS MFG. CORP.Medline — MEDLINE INDUSTRIES, INC.3M™ Cavilon™ — 3M COMPANY3M™ Cavilon™ — 3M COMPANYGluSeal® — Glustich IncKendall — Cardinal Health 200, LLCKendall — Cardinal Health, Inc.PolyMem — FERRIS MFG. CORP.GluSeal® — Glustich IncPolyMem — FERRIS MFG. CORP.PolyMem — FERRIS MFG. CORP.3M™ Cavilon™ — 3M COMPANYMedline — MEDLINE INDUSTRIES, INC.PolyMem — FERRIS MFG. CORP.3M™ Cavilon™ — 3M COMPANYCurity — Cardinal Health 200, LLCPolyMem — FERRIS MFG. CORP.Curity — Cardinal Health 200, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-06-23 | Family Dollar Stores, Llc. | Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022. |
| 2020-01-15 | Cardinal Health 200, LLC | Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization proces |
| 2011-04-04 | Smith & Nephew Inc. | Smith & Nephew, Inc., St. Petersburg, FL is recalling multiple lot numbers of the following products: REMOVE Universal Adhesive Remover Wipes, UNI-SOLVE Adhesi |
| 2007-02-14 | Coloplast Corp Skin Care Div | Coloplast Corp. is recalling Sea-Clens brands Sea-Clens wound cleaner which were found to have some particulates (foreign materials). |
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