State

Ohio product recalls

73,092 recalls have nationwide distribution and so reach Ohio. 11,753 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total: 11,753
Critical: 2,117
Severe: 2,425
Most recent: 2026-09-23

Of the 11,753 recalls naming Ohio we have scored against our rubric, 2,117 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,425 (21%) are Severe.

Which agencies issued them

These figures cover only the 11,753 recalls whose distribution notice names Ohio specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9601–9625 of 84845

HighFDA (Devices)·Z-0462-2025·2024-11-20
MEERA CL Operating Table Error Code 50037 Causes Unexpected Stoppage
The MEERA CL operating table may experience error code 50037, causing the table to unexpectedly stop during operation. This error occurs sporadically when controlled via an IR-Hand Control and may delay surgical procedures.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 700001B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0362-2025·2024-11-20
IMAGEnet 6 Ophthalmic Data System Hood Report Display Issue
IMAGEnet 6 ophthalmic software's Hood Report overlay can mislead clinicians about clinical correlations unsupported by evidence. Affects 3,144 units nationwide.
Product
The IMAGEnet 6 Ophthalmic Data System is a software program that is intended for use in the collection, storage and management of digital images, patient data, diagnostic data and clinical information from Topcon devices. It is intended for processing and displaying ophthalmic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0424-2025·2024-11-20
Halyard Vaginal Gyn Pack Recalled Due to Loose Metal Flakes Risk
AVID Medical is recalling the Halyard MAJOR VAGINAL GYN PACK due to sponge forceps and towel clamps that may shed loose metal flakes. These flakes could enter a surgical site undetected, causing local reactions or foreign body reactions.
Product
Halyard MAJOR VAGINAL GYN PACK - Medical convenience kits Model Number: SAMM021-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0366-2025·2024-11-20
Stryker electrosurgical smoke evacuation pencils recalled for unintended activation risk
Stryker is recalling smoke evacuation pencils used in electrosurgery that may activate without manual input, creating a risk of electrical burns to patients or healthcare providers.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuat
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0431-2025·2024-11-20
Halyard CPT Cardiac Cath Pack Recalled Due to Loose Metal Flakes in Forceps and Clamps
AVID Medical is recalling Halyard CPT Cardiac Cath Pack convenience kits due to small metal flakes that may detach from sponge forceps and towel clamps. Metal flakes could enter a surgical site undetected and cause local or foreign body reactions.
Product
Halyard CPT CARDIAC CATH PACK - Medical convenience kits Model Number: SHAN430-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0442-2025·2024-11-20
Halyard Pacemaker Instrument Packs Recalled for Loose Metal Flakes
AVID Medical is recalling Halyard Pacemaker Instrument Packs (Model VAPX040-01) because sponge forceps and towel clamps may contain loose metal flakes that could detach and enter a patient's surgical site during procedures.
Product
Halyard PACEMAKER INSTRUMENT PACK - Medical convenience kits Model Number: VAPX040-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0421-2025·2024-11-20
Medical Convenience Kits Recalled for Detachable Metal Flakes in Surgical Instruments
AVID Medical is recalling Halyard Shoulder Pack medical convenience kits because the sponge forceps and towel clamps contain loose metal flakes that could detach and enter a patient's surgical site during use, potentially causing foreign body reactions.
Product
Halyard SHOULDER PACK - Medical convenience kits Model Number: PANJ005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2025·2024-11-20
Halyard EYE PLASTIC TRAY Medical Kits Recalled for Loose Metal Flakes
AVID Medical recalls Halyard EYE PLASTIC TRAY medical kits due to loose metal flakes in sponge forceps and towel clamps. Metal flakes may contaminate surgical sites, potentially causing foreign body reactions or local tissue damage.
Product
Halyard EYE PLASTIC TRAY - Medical convenience kits Model Number: SAMM054-19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0327-2025·2024-11-20
Baxter AK 98 Dialysis Machine Recalled for Potential Chemical Exposure
Baxter is recalling AK 98 Dialysis Machines due to potential exposure to polychlorinated biphenyl acids and polychlorinated biphenyls.
Product
Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is Vantive.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0343-2025·2024-11-20
Imed EVA IV Fluid Bags Recalled Due to Leakage During Filling
The Metrix Company is recalling Imed EVA IV fluid bags that may leak during filling. A limited number of units have been found defective across multiple U.S. states and Canada.
Product
Imed Products Imed EVA BAG, 250 mL, 2-PORTS, REF IM68045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0356-2025·2024-11-20
UA Kit Specimen Containers Identified as Non-Sterile Despite Sterile Labeling
MEDLINE's UA Kit specimen containers are labeled as sterile but have been identified as non-sterile, posing a risk of contaminated specimens that could lead to incorrect test results and unnecessary treatment.
Product
UA KIT, SKU DYKM1690A; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0423-2025·2024-11-20
Halyard Laparotomy GYN Packs recalled due to loose metal flakes
AVID Medical recalls Halyard LAPAROTOMY GYN surgical packs due to loose metal flakes on sponge forceps and towel clamps. Metal fragments may enter the surgical site and cause local or foreign body reactions.
Product
Halyard LAPAROTOMY GYN PACK - Medical convenience kits Model Number: SAMM018-13
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0360-2025·2024-11-20
Urine kit specimen containers recalled for non-sterile condition
Medline urine kit specimen containers labeled as sterile are actually non-sterile. This risks sample contamination, infection, and unnecessary treatment.
Product
URINE KIT, SKU DYKM1845; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2025·2024-11-20
Halyard SAMMC ANGIOGRAPHY Medical Kits Recalled for Loose Metal Flakes
AVID Medical recalls Halyard SAMMC ANGIOGRAPHY medical convenience kits due to loose metal flakes on sponge forceps and towel clamps. Metal flakes may enter surgical sites, potentially causing local reactions or foreign body complications.
Product
Halyard SAMMC ANGIOGRAPHY - Medical convenience kits Model Number: SAMM066-15
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0370-2025·2024-11-20
Stryker Smoke Evacuation Pencils Recalled for Unintended Activation Risk
Stryker is recalling 403,730 Neptune SafeAir Smoke Evacuation Pencil units because they may activate unexpectedly when plugged in, creating a risk of electrical burns to patients and physicians.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button, Bulk Non-sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuatio
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2025·2024-11-20
MEERA CL Mobile Operating Table Control Malfunction Recall
The MEERA CL mobile operating table may experience error code 50037 that stops table movement during use, causing surgical procedure delays. Getinge recalled 342 units distributed worldwide.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment, Item Number: 720001B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0402-2025·2024-11-20
Medical surgical kits recalled for loose metal flakes in instruments
AVID Medical is recalling Halyard CYSTO PDS medical convenience kits due to loose metal flakes that may detach from sponge forceps and towel clamps. These flakes could enter a surgical site and cause foreign body reactions.
Product
Halyard CYSTO PDS - Medical convenience kits Model Number: GVVA002-05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0413-2025·2024-11-20
Halyard Pacemaker Pack surgical kits recalled for loose metal flakes
AVID Medical is recalling Halyard Pacemaker Pack surgical kits because sponge forceps and towel clamps contain loose metal flakes that could detach and enter patient surgical sites.
Product
Halyard PACEMAKER PACK - Medical convenience kits Model Number: MAMC223-08
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0415-2025·2024-11-20
Halyard ORTHO PACK surgical instrument kits recalled due to metal flakes
AVID Medical is recalling Halyard ORTHO PACK kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard ORTHO PACK -Medical convenience kits Model Number: MMOK006-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0355-2025·2024-11-20
Medical Laboratory Kit Recalled Due to Non-Sterile Specimen Container
Medline Industries is recalling over 626,000 laboratory kits because the included specimen container is labeled as sterile but is actually non-sterile. Non-sterile containers risk sample contamination and may result in unnecessary treatment or prolonged hospitalization.
Product
Lab Kit, SKU DYLAB1018; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0383-2025·2024-11-20
Medical Drainage Pack Components Recalled for Potential Metal Fragments
AVID Medical is recalling the Halyard IR Abcess Drainage Pack due to sponge forceps and towel clamps that may have loose metal flakes. Metal flakes could detach and enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard IR ABCESS DRAINAGE PACK - Medical convenience kits Model Number: AVMD018
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2025·2024-11-20
Halyard Angio Tray surgical kits recalled for loose metal flakes
AVID Medical recalls Halyard ANGIO TRAY (Model VAPX021-05) surgical kits due to potential loose metal flakes on forceps and clamps that could enter surgical sites and cause local or foreign body reactions.
Product
Halyard ANGIO TRAY - Medical convenience kits Model Number: VAPX021-05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0408-2025·2024-11-20
Surgical Instruments Recalled Due to Potential Metal Flake Contamination
AVID Medical recalled Halyard POST PARTUM TUBAL LIGATION surgical kit components due to loose metal flakes that could detach from sponge forceps and towel clamps. Metal flakes entering a patient's surgical site could cause local or foreign body reactions.
Product
Halyard POST PARTUM TUBAL LIGATION - Medical convenience kits Model Number: LANC026-19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0358-2025·2024-11-20
Medline Urine Collection Kits Recalled Due to Non-Sterile Specimen Containers
Medline Industries recalls 626,305 urine collection kits with non-sterile specimen containers labeled as sterile. The kits may cause unnecessary treatment or prolonged hospitalization.
Product
URINE COLLECTION KIT, SKU DYKM1848A DYKM2005 DYKM2151 DYLAB1004 DYLAB1004A DYLAB1006 DYLAB1012 ; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0391-2025·2024-11-20
Halyard Shoulder Medical Kit recalled for loose metal flakes in surgical components
AVID Medical is recalling Halyard shoulder surgical kits due to loose metal flakes that could detach and enter surgical sites. Metal debris could cause local or foreign body reactions.
Product
Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
Category
Medical Device
Distribution
Distributed nationwide