BEUDAMED
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    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962106402·SCHROEDER TENACULUM FORCEPS, 10", TIPS DO NOT O...

    HG I CUP

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWB·April 17, 2003

    UNKNOWN HGI CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 9, 2018

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·July 21, 2016

    NUTRIFILL

    FDA Adverse Event
    Injury ·CONTAMAC SOLUTIONS, INC.·Product code MRC·July 9, 2025

    UNK ZIMMER HGI CUP

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·February 20, 2013

    UNKNOWN HG I CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 20, 2019

    HG-1

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HWC·August 4, 1992

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·October 25, 2016

    UNKNOWN ZIMMER VERSYS BEADED MIDCOAT STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 9, 2018

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 9, 2018

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 9, 2018

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·May 10, 2016

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·October 27, 2016

    Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

    FDA Enforcement
    Class II ·Ongoing·Contamac Solutions, Inc.·June 18, 2025

    SUTURE

    FDA Adverse Event
    Injury ·UNK·Product code GAM·January 16, 2025

    TORIC LENS

    FDA Adverse Event
    Injury ·UNK·Product code MJP·January 16, 2025

    Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) EGD KIT, REF DYK1253578F; e) EGD REG KIT, REF DYKE1830; f) ENDO KIT, REF DYKE1516A; g) ERCP REG KIT, REF DYKM2127; h) GI PACK, REF DYKE1898; i) KIT, PEG, REG, REF DYKM2128; j) KIT,1500CC, 50CS, REF DYKM2126; k) LITHOTOMY, REF DYNJ909937; l) MAJOR BASIC, REF DYNJ909703; m) MINOR GENERAL SURGERY, REF DYNJ909940; n) SUCTION SET UP KIT, REF DYKM1187A; o) TURNOVER KIT, REF DYKC1274A; p) TURNOVER KIT MKT STRAPS, REF DYKC1309A; q) U BAR, REF DYNJ902374K

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code LRO·March 22, 2024

    NUTRIFILL

    FDA Adverse Event
    Injury ·CONTAMAC SOLUTIONS, INC.·Product code MRC·June 24, 2025

    NUTRIFILL

    FDA Adverse Event
    Injury ·CONTAMAC SOLUTIONS, INC.·Product code MRC·June 24, 2025