BEUDAMED
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    Olympus POWERSEAL 5MM, 37CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION Model Number: PS-0537CJDA. An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code GEI·August 12, 2022

    Olympus POWERSEAL 5MM, 44CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION Model Number: PS-0544CJDA. An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code GEI·August 12, 2022

    Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

    FDA Recall
    Open, Classified ·Product code NUJ·October 1, 2025

    Medline Renewal LigaSure Impact Curved Large Jaw Sealer/Divider, Compatible with FT10 Generator, FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

    FDA Recall
    Open, Classified ·Product code NUJ·October 1, 2025

    Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

    FDA Recall
    Open, Classified ·Product code NUJ·October 1, 2025

    Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

    FDA Recall
    Open, Classified ·Product code NUJ·October 1, 2025

    Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

    FDA Recall
    Open, Classified ·Product code NUJ·October 1, 2025

    FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685

    FDA Recall
    Open, Classified ·Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany·Product code FCL·March 24, 2023

    RAPIDSORB IPS Battery Pack, Sterile-Intended for use in non-load bearing fracture repair and reconstructive procedures of the craniofacial skeleton (excluding the upper and lower jaw) in pediatric and adult populations. Part Number: 530.553.01S

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code HBW·January 24, 2024

    Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-CVD190MM; (3) REF BH957R, Schnidt Tonsil Forceps SLT-CVD185MM; (4) REF BH959R, Schnidt Tonsil Forceps CVD 185MM; (5) REF BH961R, Schnidt Tonsil FCPSOPEN-RINGCVD 185MM; (6) REF BH963R, Schnidt Tonsil FCPSOPEN-RINGCVD185MM; and (7) REF BH965R, Wilson Tonsil Forceps 190MM.

    FDA Recall
    Open, Classified ·Aesculap Inc·Product code KAE·January 31, 2025

    POWERSEAL 5 mm, 37 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0537CJDA

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code GEI·March 7, 2024

    POWERSEAL 5 mm, 23 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0523CJDA

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code GEI·March 7, 2024

    POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general surgery and such surgical specialties as urologic, colorectal, bariatric, vascular, thoracic, and gynecologic. Model/Catalog Number: PS-0544CJDA

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code GEI·March 7, 2024

    Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model Numbers: VH-4001. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code GEI·December 9, 2024

    VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive surgery allowing access for vessel harvesting.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code GEI·December 9, 2024

    LotFancy Urinary Tract Infection Urine (UTI) Test Strips; PALINOIA UTI-10 PARAMETER REAGENT STRIPS; Vaunn Medical 8-in-1 Urinalysis Reagent Strip; JNW Direct 4-in-1 UTl Urinalysis Test Strips; Urinify STRENGTH; Urinify ESSENTIAL, Urinify Urinary Tract Infection (UTI)

    FDA Recall
    Open, Classified ·Changchun Wancheng Bio-Electron Co., Ltd. 2336, Tianwei Road Beihu Science and Technology Development Zone Changchun China·Product code LJX·November 22, 2025

    Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2) REF FB459R, Glover ATR.CLAMP CVD 245MM; (3) REF FB461R, Glover ATR.CLAMP 195MM; (4) REF FB462R, Glover ATR.CLAMP 210MM; (5) REF FB469R, Leland-Jones Peripheral CLMPSTR 195MM; (6) REF FB567R, Cooley Pediatric Clamp 30DG30/165MM; (7) REF FB568R, Cooley Pediatric Clamp 60DG 30/160MM; (8) REF FB569R, Cooley Pediatric Clamp 90DG30/150MM; (9) REF FB729R, Cooley Pediatric Clamp 17MM 170MM; (10) REF FB730R, Cooley Pediatric Clamp 20MM175MM; (11) REF FB736R, Cooley Pediatric Clamp 74MM 185MM; (12) REF FB737R, Cooley Pediatric Clamp 86MM 195MM; and (13) REF FB738R, Cooley Pediatric Clamp 108MM 260MM.

    FDA Recall
    Open, Classified ·Aesculap Inc·Product code HXD·January 31, 2025