Class IIOngoingZ-1574-2026
LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft
Labeling mix-up resulting in the incorrect lot outer packaging of product.
LeMaitre Vascular, Inc…NJMar 25, 2026
All device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,105–1,116 of 4,586 recalls
Class IIOngoingZ-1573-2026
Baxter Healthcare Corporation recalls Brand Name: Welch Allyn
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
Baxter Healthcare Corp…ILMar 25, 2026
Class IIOngoingZ-1572-2026
Howmedica Osteonics Corp. recalls MICS3 Angled Sagittal Saw Attachment
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment.…
Howmedica Osteonics Co…NJMar 25, 2026
Class IIOngoingZ-1571-2026
GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individ…
GE Medical Systems, LL…WIMar 25, 2026
Class IIOngoingZ-1570-2026
GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individ…
GE Medical Systems, LL…WIMar 25, 2026
Class IIOngoingZ-1569-2026
GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individ…
GE Medical Systems, LL…WIMar 25, 2026
Class IIOngoingZ-1565-2026
Abbott Diagnostics Scarborough, Inc. recalls Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Versio…
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
Abbott Diagnostics Sca…MEMar 25, 2026
Class IIOngoingZ-1564-2026
Medline Industries, LP recalls Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care.…
Medline Industries, LPILMar 18, 2026
Class IIOngoingZ-1563-2026
Medline Industries, LP recalls Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care.…
Medline Industries, LPILMar 18, 2026
Class IIOngoingZ-1562-2026
Medline Industries, LP recalls Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART
The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.
Medline Industries, LPILMar 18, 2026
Class IIOngoingZ-1561-2026
Altruan GmbH recalls Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal antige…
Product not cleared by the FDA.
Altruan GmbHMar 18, 2026
Class IIOngoingZ-1560-2026
Altruan GmbH recalls Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci…
Product not cleared by the FDA.
Altruan GmbHMar 18, 2026