Class IIOngoingZ-2448-2026
Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System
There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
Steris CorporationOHJun 24, 2026
Recalls in Ohio
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 25–36 of 109 recalls
Class IIOngoingZ-2295-2026
Daavlin Distributing Company recalls Phothera 200
Some of the Calibration/Output Certificates had the outputs reversed.
Daavlin Distributing C…OHJun 10, 2026
Class IIOngoingZ-2239-2026
Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker
Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.
Devicor Medical Produc…OHJun 3, 2026
Class IIOngoingZ-2171-2026
Aniara Diagnostica LLC recalls ZYMUTEST HIA IgG
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
Aniara Diagnostica LLCOHMay 20, 2026
Class IOngoingZ-1981-2026
American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating A…
Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold.…
American Contract Syst…OHMay 13, 2026
Class IIOngoingZ-1815-2026
3B Medical, Inc. recalls React Health PHOENIX 5L Oxygen Concentrator
Devices which did not meet internal quality specifications were inadvertently distributed.
3B Medical, Inc.OHApr 22, 2026
Class IIOngoingZ-1361-2026
Steris Corporation recalls Barco MNA with the HexaVue IP Integration System
This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.
Steris CorporationOHFeb 18, 2026
Class IIOngoingZ-1202-2026
Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems…
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
Zimmer Surgical IncOHFeb 4, 2026
Class IIOngoingZ-1201-2026
Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems…
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
Zimmer Surgical IncOHFeb 4, 2026
Class IIOngoingZ-1019-2026
Meridian Bioscience Inc recalls Revogene C. difficile
The affected lots show a decline in performance over time, which may lead to false-negative results.
Meridian Bioscience In…OHJan 14, 2026
Class IIOngoingZ-0925-2026
Zimmer Surgical Inc recalls Zimmer Dermatome AN
The devices may have a misaligned thickness control bar.
Zimmer Surgical IncOHDec 24, 2025
Class IIOngoingZ-0924-2026
Zimmer Surgical Inc recalls Zimmer Air Dermatome
The devices may have a misaligned thickness control bar.
Zimmer Surgical IncOHDec 24, 2025