20 results
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14ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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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