LLKClass II

Legging, Compression, Non-inflatable

General Hospital · 21 CFR 880.5780

MDR events25All time

Recalls1All time

Registered firms8Currently listed

510(k) clearances4All time

Recent MDR events

25 adverse event reports on file

Event type breakdown

Injury17

Malfunction7

Other1

Most-reported manufacturers

Medtronic Neuromodulation18 Jobst Institute2 Bsn Medical, Inc.1 Kendall1 Medtronic, Inc.1 Rice Creek Manufacturing1 Rice Creek Mfg1

Recalls

1 recall events for this product code

Customed, Inc
TerminatedDec 16, 2014
Wound Management Tray Ryder Memorial, Catalog number 900-1456.
Customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.
Z-0254-2015 · View FDA record ↗

Registered firms

8 firms currently registered for this product code

510(k) clearances

4 clearances for this product code