State

Ohio product recalls

72,966 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 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5676–5700 of 84689

HighFDA (Devices)·Z-2519-2025·2025-09-10
Sterile cover kits recalled because elastic bands may detach during surgery
Sterile Cover 10-Pack Shipper Box Assemblies are recalled because elastic bands in the kit may detach or fracture during surgery, risking retained foreign bodies and surgical site infection. 200 units are affected.
Product
Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Model/Catalog Number: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Software Version: Not Applicable Product Description: Sterile Cover
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2511-2025·2025-09-10
MediHoney surgical adhesive sheets recalled over sterile barrier packaging failures
MediHoney HCS Surgical Adhesive Sheet dressings, catalog number 31738, lot 53824, are recalled after packaging failures were identified that could breach the sterile barrier. 4 units are affected.
Product
Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Surgical Adhesive Sheet Model/Catalog Number: 31738 Product Description: MEDIHONEY¿ HCS SURGICAL ADHESIVE SHEET DRESSINGS with LEPTOSPERMUM HONEY is a moist wound dressing made of Leptospermum Honey (+15) in combination with
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0553-2025·2025-09-10
Coconut breaded butterfly shrimp recalled over possible cesium-137 contamination
Clean-tail Coconut Farm Raised Breaded Butterfly Shrimp in bulk master cartons, product of Indonesia, is recalled because it may be contaminated with Cesium-137. 31 cases are affected.
Product
Clean-tail Coconut Farm Raise Breaded Butterfly Shrimp Clean Tail (21/25 CT per pound) in bulk packaging, corrugated master cartons. Master carton case (4 x 3lb), KEEP FROZEN. Product of Indonesia, Item# 1SH0468709H
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-2509-2025·2025-09-10
MediHoney non-adhesive hydrogel dressings recalled over sterile barrier packaging failures
MediHoney Non-Adhesive Hydrogel Sheet Dressings, catalog numbers 31620 and 31640, are recalled after packaging failures were identified that could breach the sterile barrier. 5,374 units are affected.
Product
Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Model/Catalog Number: 31620, 31640 Product Description: MEDIHONEY¿ Non-Adhesive Hydrogel Sheet Dressing with Leptospermum Honey is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydrogel ge
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V589000·2025-09-10
Volvo Recalls 2026 Models Due to Damaged Front Seat Belt Retractors
Volvo is recalling 2026 V60, V90, XC60, and XC90 models because damaged seat belt retractors may fail to restrain occupants in a crash.
Product
VOLVO — VOLVO V60CCMHEV, V90CCMHEV, XC60MHEV, redundant XC90MHEV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2521-2025·2025-09-10
Tumor profiling assay recalled after incorrect result gave wrong therapy recommendation
One MI Cancer Seek tumor mutational profiling assay is recalled because an incorrect test result was provided that indicated the incorrect drug therapy recommendation.
Product
MI Cancer Seek REF MSC000 UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Seek is a single-site assay intended to provide tumor mutational profiling to be used by qualified healthcare professionals in accordance with professional oncology guidelines for cancer patients wi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0608-2025·2025-09-10
Compounded semaglutide 0.8 mL vials recalled after testing subpotent
Semaglutide 2.5 mg/mL injection, 0.8 mL, from Boothwyn Pharmacy is recalled nationwide as a subpotent drug. 186 vials are affected.
Product
Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0552-2025·2025-09-10
Cleantail breaded butterfly shrimp recalled over possible cesium-137 contamination
Admiral of the Fleet and Portico Seafood Classic cleantail breaded butterfly shrimp in bulk master cartons is recalled because it may be contaminated with Cesium-137. 1,200 cases are affected.
Product
ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC (SYSCO) Cleantail Breaded Butterfly Shrimp (16/20 CT per pound) in bulk packaging, corrugated master cartons. Master carton case is NET WT 12 lbs. (192 OZ) 5.44 kg (4 x 3lbs cartons), and carton case (4 x 3lb (1.36 kg), KEEP FROZEN
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-2513-2025·2025-09-10
External fixation universal joints recalled because pins may become dislodged
Medshape Universal Joints, REF DNE-9000-UJ, are recalled because a pin in the bone external fixation system can become dislodged, causing frame instability. 849 units are affected.
Product
Medshape Universal Joints, REF: DNE-9000-UJ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0614-2025·2025-09-10
KIMMTRAK injection recalled after testing subpotent in three affected lots
KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, is recalled nationwide as a subpotent drug. 7,572 vials are affected.
Product
KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd by: Immunocore Limited, 92 Park Drive, Abingdon, Oxfordshire, OX14 4RY, United Kingdom, For: Immunocore Commercial LLC, 181 Washington St, Conshohocken, PA, 19428
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2505-2025·2025-09-10
MediHoney paste tubes 31505 recalled over packaging failures affecting sterility
MediHoney Paste, catalog number 31505, is recalled after packaging failures were identified that could lead to a breach in the sterile barrier. 15,441 units are affected.
Product
Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist environment con
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2512-2025·2025-09-10
CVS honey wound pads recalled over packaging failures breaching sterile barrier
CVS Honey Pads, catalog numbers 9370613 and 937404, are recalled after packaging failures were identified that could lead to a breach in the sterile barrier. 111,492 units are affected.
Product
Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Product Description: Infused with natural medical-grade honey Manuka (Leptospermum) honey is a medical-grade honey that is harvested from bees in New Zealand. Researchers have found
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2499-2025·2025-09-10
Defibrillator recalled because required post-service inspections were not performed
One LIFEPAK CR2 defibrillator is recalled because required inspections were not performed on units that had gone through servicing.
Product
LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 99512-001434 883873785911 LIFEPAK CR2: The LIFEPAK CR2 defibrillator is indicated for use on patients 1 year of age or older in cardiopulmonary arrest. The patient must be unresponsive (unconscious), not breathin
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2489-2025·2025-09-10
RayStation 9B and 10A software recalled over non-unique DICOM identifiers
RayStation 9B, 9B SP1, 10A and 10A service pack radiation therapy planning software is recalled because DICOM instance identifiers from the RayGateway interface are not guaranteed to be unique.
Product
RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.933. 2. RayStation 9B Service Pack 1, Software Version: 9.2.0.483. 3. RayStation 10A, Software Version: 10.0.0.1154. 4. RayStation 10A Service Pack 1, Software Version: 10.0
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2497-2025·2025-09-10
LIFEPAK 15 defibrillators recalled because post-service inspections were not performed
Four LIFEPAK 15 defibrillators are recalled because required inspections were not performed on units that had gone through servicing.
Product
LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-2-000099 / 99577-000093 / 883873979020 V15-2-001603 / 99577-001256 / 883873911631 LIFEPAK 15: The LP15 is intended for use by trained
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0618-2025·2025-09-10
Chlorpromazine 100 mg tablets recalled over micro-organism on packaging coil
Amneal chlorpromazine hydrochloride tablets, 100 mg, are recalled because a micro-organism was detected on a lot of auxiliary polyester coil used in packaging. No micro-organism was found on any tablets.
Product
CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0616-2025·2025-09-10
Chlorpromazine 25 mg tablets recalled after micro-organism found on packaging coil
Amneal chlorpromazine hydrochloride tablets, 25 mg, are recalled because a micro-organism was detected on a lot of auxiliary polyester coil used in packaging. No micro-organism was found on any tablets.
Product
CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2516-2025·2025-09-10
Spinal implant inserters recalled over potential missing pins at the tip
TOPS Inserters, model 82889, part of the TOPS System Instrument Set, are recalled because of the potential for missing pins at the tip of the inserter. 30 units are affected.
Product
TOPS Inserter, part of the TOPS System Instrument Set used for implantation of the TOPS System. Model Number: 82889.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0607-2025·2025-09-10
Compounded fluorescein ophthalmic solution recalled after testing subpotent in one lot
Fluorescein 2% Ophthalmic, 3 mL, from Boothwyn Pharmacy is recalled nationwide as a subpotent drug. 8 vials are affected.
Product
Fluorescein 2% Ophth, 3 ML, Boothwyn Pharmacy, 800-476-7496
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2488-2025·2025-09-10
RayStation 8B and 9A software recalled over DICOM identifier uniqueness defect
RayStation 8B, its service packs and 9A radiation therapy planning software is recalled because DICOM instance identifiers from the RayGateway interface are not guaranteed to be unique.
Product
RayStation with the following product descriptions: 1. RayStation 8B, Software Version: 8.1.0.47. 2. RayStation 8B Service Pack 1, Software Version: 8.1.1.8. 3. RayStation 8B Service Pack 2, Software Version: 8.1.2.5. 4. RayStation 9A, Software Version: 9.0.0.113.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2495-2025·2025-09-10
RayStation 2023B and 2024A software recalled over non-unique DICOM identifiers
RayStation 2023B, 2024A and 2024A SP3 radiation therapy planning software is recalled because DICOM instance identifiers from the RayGateway interface are not guaranteed to be unique.
Product
RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.0.3338. 2. RayStation 2024A, Software Version: 15.0.0.430. 3. RayStation 2024A SP3, Software Version: 15.1.3.10. Product Description: Radiation Therapy Treatment Plannin
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2492-2025·2025-09-10
RayStation 11B software recalled over non-unique DICOM instance identifiers
RayStation 11B and its service packs are recalled because DICOM instance identifiers from the RayGateway interface to Accuray's iDMS are not guaranteed to be unique.
Product
RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.932. 2. RayStation 11B Service Pack 1, Software Version: 12.1.0.1221. 3. RayStation 11B Service Pack 2, Software Version: 12.0.3.68. 4. RayStation 11B Service Pack 3, Soft
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2501-2025·2025-09-10
Uric acid monitoring kits recalled over missing premarket clearance or approval
A second lot group of Blood Uric Acid Monitoring System kits, model eB-U01, covering all lots made up to June 20, 2022, is recalled for distribution without premarket clearance. 2,580 units are affected.
Product
Blood Uric Acid Monitoring System Each kit contains 1 meter, 1 lancing device, user manual, 10 lancets, and 10 test strips (10-count bottle)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2504-2025·2025-09-10
Fluoroscopic X-ray systems recalled over air baffle missing from internal PCs
Philips Allura Xper interventional fluoroscopic X-ray systems are recalled because an air baffle component may be missing in some Nehalem FlexVision-2 PCs. 192 units are affected.
Product
Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series. Labeled as the following with corresponding model numbers: 1. Allura Xper FD10, Model Number 722003. 2. Allura Xper FD10/10, Model Number 722005. 3. Allura Xper FD20, Model Number 722006. 4. All
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0615-2025·2025-09-10
Sulfamethoxazole and trimethoprim tablets recalled over micro-organism on packaging coil
Amneal sulfamethoxazole and trimethoprim double strength tablets are recalled because a micro-organism was detected on a lot of auxiliary polyester coil used in packaging. No micro-organism was found on any tablets.
Product
SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
Category
Drug
Distribution
Distributed nationwide