Class IIOngoingZ-3019-2026
Medline Industries, LP recalls Medline convenience kits labeled as: 1) FEMORAL PACK
Kits contain a potentially contaminated component which were recalled by the manufacturer
Medline Industries, LPILSep 2, 2026
2026 device recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 85–96 of 2,088 recalls
Class IIOngoingZ-3018-2026
ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B…
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
ConMed CorporationNYSep 2, 2026
Class IIOngoingZ-3017-2026
Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Medical Care
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines.
Fresenius Medical Care…MASep 2, 2026
Class IIOngoingZ-3016-2026
Henry Schein Inc. recalls Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
Henry Schein Inc.PASep 2, 2026
Class IIOngoingZ-3015-2026
Henry Schein Inc. recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
Henry Schein Inc.PASep 2, 2026
Class IIOngoingZ-3014-2026
Canon Medical System, USA, INC. recalls Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiogr…
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.
Canon Medical System,…CASep 2, 2026
Class IIOngoingZ-3013-2026
Midmark Corporation recalls Midmark Digital ECG HD+12
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Midmark CorporationOHSep 2, 2026
Class IIOngoingZ-3012-2026
Midmark Corporation recalls Midmark IQecg Digital ECG
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Midmark CorporationOHSep 2, 2026
Class IIOngoingZ-3011-2026
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
AVID Medical, Inc.VASep 2, 2026
Class IIOngoingZ-3010-2026
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
AVID Medical, Inc.VASep 2, 2026
Class IIOngoingZ-3009-2026
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
AVID Medical, Inc.VASep 2, 2026
Class IIOngoingZ-3008-2026
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
AVID Medical, Inc.VASep 2, 2026