20 results · 14ms · Sources: EU EUDAMED, US FDA

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Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Column Distal Radius Plate - 6 Head, 10 Shaft, Standard Left - 139mm

FDA Recall
Open, Classified ·Tyber Medical·Product code HRS·December 19, 2025

Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Column Distal Radius Plate - 6 Head, 14 Shaft, Standard Left - 186mm Component: No

FDA Recall
Open, Classified ·Tyber Medical·Product code HRS·December 19, 2025

HENRY SCHEIN CRITERION EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)

FDA Recall
Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code FXX·December 21, 2023

Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C

FDA Recall
Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code EFQ·May 8, 2026

Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in, Non-Sterile/55994C; 0.75x0.75in, Non-Sterile/55995C; 1.0x1.0in, Non-Sterile/55996C; 1.0x3.0in, Non-Sterile/55997C; 0.5x1.5in, Non-Sterile/55998C

FDA Recall
Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code EFQ·May 8, 2026

PATTERSON PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)

FDA Recall
Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code FXX·December 21, 2023

HENRY SCHEIN CRITERION ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)

FDA Recall
Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code FXX·December 21, 2023

Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116

FDA Recall
Open, Classified ·Beckman Coulter Inc.·Product code CDD·July 28, 2021

Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO

FDA Recall
Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000, 1107-9610-000, 1107-9612-000, 1107-9616-000, 1107-9617-000, 2066835-001, 2069767-001, 2078800-001, 2091008-001, 2091009-001, M1098876, M1145610, M1220023, M1220854, M1221495, and M1233992

FDA Recall
Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.

FDA Recall
Open, Classified ·Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany·Product code CDD·July 17, 2024

Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.

FDA Recall
Open, Classified ·Draeger, Inc.·Product code CAD·November 24, 2025

QUCARE Total Cholesterol in vitro diagnostic test REF: 6407

FDA Recall
Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code CHH·April 2, 2026

Tec 850 SEV Anesthesia Vaporizer, Reference Number 1177-9850-SEV

FDA Recall
Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

PE Centrifuge, REF: B36365, a component of the Power Express

FDA Recall
Open, Classified ·Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany·Product code CDD·July 17, 2024

Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer.

FDA Recall
Open, Classified ·Draeger, Inc.·Product code CAD·November 24, 2025

Tec 820 ISO Anesthesia Vaporizer, Reference Number 1177-9820-ISO

FDA Recall
Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

Tec 820 SEV Anesthesia Vaporizer, Reference Number 1177-9820-SEV

FDA Recall
Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825

FDA Recall
Open, Classified ·Beckman Coulter Inc.·Product code CHH·November 10, 2021

Power Express, REF B90918

FDA Recall
Open, Classified ·Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany·Product code CDD·July 17, 2024