BEUDAMED
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    LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit

    FDA Recall
    Open, Classified ·LSL Healthcare Inc.·Product code OWL·December 22, 2025

    LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131

    FDA Recall
    Open, Classified ·LSL Healthcare Inc.·Product code LRS·March 9, 2026

    CALM software, version 02.09.01 This software is intended for use as a central monitoring system with signal analysis and remote repeaters in the perinatal clinical environment. It interfaces with standard fetal and maternal monitors and provides fetal surveillance, monitoring of labor progress, charting, reporting and data analysis, display and archiving functions.

    FDA Recall
    Terminated ·LMS Medical Systems Ltd·Product code HGM·January 11, 2005

    LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·February 4, 2026

    Pathfast D-Dimer, Reference number: PF1051-KUS

    FDA Enforcement
    Class II ·Terminated·Lsi Medience Corporation·November 30, 2016

    Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4; Simplify Disc Size 2, Ht 5/MD-5; Simplify Disc Size 2, Ht 5, 5/MD-5L; Simplify Disc Size 2, Ht 6/MD-6; Simplify Disc Size 2, Ht 6, 5/MD-6L; Simplify Disc Size 3, Ht 5/LG-5; Simplify Disc Size 3, Ht 5, 5/LG-5L; Simplify Disc Size 3, Ht 6/LG-6; Simplify Disc Size 3, Ht 6, 5/LG-6L

    FDA Enforcement
    Class II ·Ongoing·NuVasive Inc·August 3, 2022

    Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M; 2) SM-SPINE PACK-LF, Kit SKU DYNJ0395037X; 3) TOTAL HIP PACK, Kit SKU DYNJ04809N; 4) MAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN; 5) SCC/SPOC HAND & FOOT PACK, Kit SKU DYNJ27164Q; 6) ORTHO SPINE, Kit SKU DYNJ40221G; 7) URO GYN PACK, Kit SKU DYNJ45311J; 8) LAMINECTOMY PACK, Kit SKU DYNJ46330C; 9) DJ ORTHO SPINE, Kit SKU DYNJ48980M; 10) CERVICAL PACK, Kit SKU DYNJ52995F; 11) NORTH BACK FUSION PACK-LF, Kit SKU DYNJ56483L; 12) KNEE ARTHROSCOPY CHRISTUS, Kit SKU DYNJ61200B; 13) KNEE ARTHROSCOPY PACK-LF, Kit SKU DYNJ66150; 14) HIP PACK, Kit SKU DYNJ66630; 15) OHNS FREE FLAP A PACK, Kit SKU DYNJ69065F; 16) LUMBAR PACK, Kit SKU DYNJ69113C; 17) LAMINECTOMY PACK, Kit SKU DYNJ69401D; 18) LAMINECTOMY PACK, Kit SKU DYNJ81013D; 19) HIP/SHOULDER ARTHROSCOPY PACK, Kit SKU DYNJ84275A; 20) FLASC ACL PACK, Kit SKU DYNJ88971; 21) SPINE PACK MERCY GALENA, Kit SKU DYNJ89943; 22) SPINAL FUSION MT CARMEL, Kit SKU DYNJ900173J; 23) HAND, Kit SKU DYNJ904945G; 24) LAMINECTOMY, Kit SKU DYNJ909505D; 25) SHOULDER SPLIT, Kit SKU DYNJ910543F; 26) SHOULDER SPLIT, Kit SKU DYNJ910543G; 27) CRANIOTOMY PACK, Kit SKU DYNJT4724; 28) SPINE PACK, Kit SKU DYNJT5184.

    FDA Recall
    Open, Classified ·Product code OJH·December 12, 2025

    Radioimmunoassay, Lsd (125-I)

    FDA classification
    FDA Class 2 ·Radioimmunoassay, Lsd (125-I)

    Free Radical Assay, Lsd

    FDA classification
    FDA Class 2 ·Free Radical Assay, Lsd

    Pathfast D-Dimer, Reference number: PF1051-KUS

    FDA Recall
    Terminated ·Lsi Medience Corporation 13-4 Uchikanda·Product code GHH·August 16, 2016

    NSSA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FSM·October 25, 2016

    SIG HP PATELLA & INSERTION CSE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code FSM·October 26, 2016

    MATRIXNEURO INSTRUMENT MODULE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FSM·October 7, 2016

    MATRIXNEURO INSTRUMENT MODULE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FSM·October 7, 2016