State

Ohio product recalls

72,969 recalls have nationwide distribution and so reach Ohio. 11,723 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total: 11,723
Critical: 2,107
Severe: 2,413
Most recent: 2026-09-16

Of the 11,723 recalls naming Ohio we have scored against our rubric, 2,107 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,413 (21%) are Severe.

Which agencies issued them

These figures cover only the 11,723 recalls whose distribution notice names Ohio specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6126–6150 of 84692

HighFDA (Devices)·Z-2222-2025·2025-08-06
Osteotec silicone finger implants may contain foreign material
Osteotec Silicone Finger Implants in sizes 3, 4 and 5 are being recalled because there is the potential that the silicone implant may contain foreign material. 15,573 units are affected.
Product
Brand Name: Osteotec Product Name: Osteotec Silicone Finger Implant Model/Catalog Number: OSTF-3 (Sz. 3), OSTF-4 (Sz. 4), OSTF-5 (Sz. 5) Software Version: N/A Product Description: The Osteotec Silicone Finger Implant is a one-piece, sterile, flexible silicone elastomer implan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2177-2025·2025-08-06
HarmonyAIR dual flat panel monitor yokes may detach from spring arm
Dual Flat Panel Monitor accessories for HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the yoke assembly may detach from the spring arm. 167 units are affected.
Product
Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR A-Series Surgical Lighting Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2213-2025·2025-08-06
Philips MR 5300 gradient coils may act as a heat source
MR 5300 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 551 units are affected.
Product
MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2204-2025·2025-08-06
Philips Ingenia 1.5T gradient coils may act as a heat source
Ingenia 1.5T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 2,279 units are affected.
Product
Ingenia 1.5T Model Numbers (REF): (1) 781315, (2) 718641, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2200-2025·2025-08-06
Philips Achieva 3.0T gradient coils may act as a heat source
Achieva 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 460 units are affected.
Product
Achieva 3.0T; Model Numbers (REF): (1) 781177, (2) 781277, (3) 781278, (4) 781344, (5) 781345;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0545-2025·2025-08-06
Bicillin L-A 2.4 million unit vials recalled after particulates found
Bicillin L-A (penicillin G benzathine injectable suspension) 2,400,000 units per 4 mL is being recalled because of CGMP deviations, with particulates identified during visual inspection. 19,279 vials affected.
Product
BICILLIN L-A — BICILLIN L-A (PENICILLIN G BENZATHINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2217-2025·2025-08-06
SmartPath to Ingenia Elition X gradient coils may overheat
SmartPath to Ingenia Elition X systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 33 units affected.
Product
SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2230-2025·2025-08-06
RAPIDPoint 500 wash waste cartridge lot biases seven blood analytes
A lot of RAPIDPoint 500 Systems Wash/Waste Cartridges is being recalled because a manufacturing error causes positive and negative bias across seven analytes. 1,477 units are affected.
Product
RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number: 10329097.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2201-2025·2025-08-06
Philips Achieva XR gradient coils may act as a heat source
Achieva XR MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 40 units are affected.
Product
Achieva XR; Model Numbers (REF): (1) 781153, (2) 781253;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2233-2025·2025-08-06
LVP blood administration sets have potential for external cassette leaks
LVP Blood Products Administration Sets are being recalled because of the potential for external cassette leaks. 14,280 units are affected.
Product
LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2175-2025·2025-08-06
Inseego dongle kit flash drives carry outdated patient monitor software
Inseego USB8 4G Dongle Kits for the Tempus Pro Monitor are being recalled because the kit's USB flash drive contains outdated software that could revert the monitor and reintroduce a previous issue. 55 units affected.
Product
Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2234-2025·2025-08-06
LVP primary administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Single Outlet Low Sorbing, are being recalled because of the potential for external cassette leaks. 35,925 units are affected.
Product
LVP Primary Administration Set, Single Outlet Low Sorbing (Qty 25). Product Code: SET-0021-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2198-2025·2025-08-06
CoSense sampling sets may carry residual carbon monoxide from insufficient aeration
Precision Sampling Sets for the CoSense End-Tidal Carbon Monoxide Monitor are being recalled because residual carbon monoxide may remain in the cannula filter, which may raise ETCOc scores. 2,160 units affected.
Product
Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide Monitor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2206-2025·2025-08-06
Philips Ingenia 3.0T gradient coils may act as a heat source
Ingenia 3.0T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 1,467 units are affected.
Product
Ingenia 3.0T Model Numbers (REF): (1) 781342, (2) 781377, (3) 782103;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2224-2025·2025-08-06
Strep Selective II Agar plates may carry Listeria monocytogenes contamination
Strep Selective II Agar, product number R01859, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 371 units are affected.
Product
Strep Selective II Agar, Product Number R01859
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2211-2025·2025-08-06
Philips Ingenia Elition X gradient coils may act as heat source
Ingenia Elition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 632 units are affected.
Product
Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2235-2025·2025-08-06
LVP dual Y-site administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site, are being recalled because of the potential for external cassette leaks. 348,150 units are affected.
Product
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Product Code: SET-0032-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2178-2025·2025-08-06
HarmonyAIR E-Series monitor yokes may detach from the spring arm
Dual Flat Panel Monitor accessories for HarmonyAIR E-Series Surgical Lighting Systems are being recalled because the yoke assembly may detach from the spring arm. 59 units are affected.
Product
Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2223-2025·2025-08-06
Blood agar plates may carry Listeria monocytogenes surface contamination
Blood Agar with 5% Sheep Blood, product number R01202, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 1,552 units affected.
Product
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2218-2025·2025-08-06
Philips MR 7700 upgrade gradient coils may act as a heat source
Upgrade to MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 26 units are affected.
Product
Upgrade to MR 7700 Model Number (REF): 782130;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2226-2025·2025-08-06
Blood MacConkey biplates may carry Listeria monocytogenes surface contamination
Blood/MacConkey Biplates, product number R02049, are being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 611 units are affected.
Product
Blood/MacConkey Biplate 100/PK, Product Number R02049
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2174-2025·2025-08-06
HeartSine samaritan public access defibrillators may not deliver shocks properly
HeartSine SAM 350P, 360P and 450P public access defibrillators are being recalled because a component manufacturing issue means the device may not function properly to deliver shocks. 190,516 units affected.
Product
HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access Defibrillator)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2225-2025·2025-08-06
Blood EMB Levine plates may carry Listeria monocytogenes contamination
Blood/EMB Levine plates, product number R02041, are being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 750 units are affected.
Product
Blood/EMB, Levine 100/PK, Product Number R02041
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2216-2025·2025-08-06
SmartPath to dStream XR gradient coils may act as heat source
SmartPath to dStream for XR and 3.0T systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 294 units affected.
Product
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2209-2025·2025-08-06
Philips Ingenia Ambition X gradient coils may act as heat source
Ingenia Ambition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 690 units are affected.
Product
Ingenia Ambition X Model Numbers (REF): (1) 781356, (2) 782109, (3) 782138;
Category
Medical Device
Distribution
Distributed nationwide