State

Ohio product recalls

20,364 recalls have nationwide distribution and so reach Ohio. 0 additional recalls listed Ohio specifically in their distribution scope.

About recalls in Ohio

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Ohio consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14926–14950 of 20364

HighFDA (Devices)·Z-0720-2023·2022-12-21
Cordis Angiographic Catheter Extensions Recalled for Male Connector Separation Risk
Cordis angiographic catheter extensions may experience separation at the male connector during use. Approximately 2,915 US units were distributed; users should verify affected lot numbers.
Product
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2023·2022-12-21
STRADIS HEALTHCARE Eye Surgical Kits Recalled for Incomplete Sealing
STRADIS HEALTHCARE WECKCELL EYE SPEARS surgical kits (Item 9430, 9431) are recalled due to incomplete outer bag sealing that may compromise kit sterility. Approximately 80 kits distributed in the US and Canada are affected.
Product
STRADIS HEALTHCARE, WECKCELL EYE SPEARS, Item Numbers: a) 9430, b) 9431
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0541-2023·2022-12-21
Surgical procedure kits recalled for incomplete seal and potential sterility breach
Stradis Healthcare is recalling medical surgical procedure trays and kits with potentially incomplete outer bag seals that could compromise sterility. These products were distributed nationwide in the US and Canada.
Product
STRADIS HEALTHCARE, Vasc Vein, Item No.682-1583,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2023·2022-12-21
Dental Surgical Pack Recalled Due to Incomplete Sterile Seal
Stradis Medical is recalling a dental surgical pack because the outer bag may be incompletely sealed, potentially compromising sterility. Affected units should not be used.
Product
Surgical room, DENTAL SURGICAL PACK, Item No.41236SDSP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0520-2023·2022-12-21
Medical procedure trays recalled for incomplete outer bag sealing
Stradis Medical recalls Henry Schein temp stimulator supplies due to incomplete outer bag sealing that may compromise kit sterility. Affected units should not be used until reviewed.
Product
HENRY SCHEIN, TEMP STIMULATOR SUPPLIES, Item No.570-2883
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0533-2023·2022-12-21
Surgical procedure trays with incomplete outer bag seals recalled
Stradis Healthcare is recalling Henry Schein labiaplasty procedure kits due to incomplete outer bag seals that could compromise sterility. The 42-unit recall affects products distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, Labiaplasty PackItem No.570-3118,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2023·2022-12-21
Leica Provido surgical microscope models at risk of unexpected power shutdown
Leica Provido surgical microscope systems may experience unexpected shutdown due to power supply overheating. Affected units should be identified by serial number and serviced immediately.
Product
Leica MICROSYSTEMS Provido, Part Numbers 10448950 (Premium), 10448976 (Standard). Surgical microscope system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2023·2022-12-21
Single-shot epidural kits recalled due to incomplete outer bag sealing
Stradis Medical is recalling 80 Henry Schein single-shot epidural kits due to potentially incomplete outer bag sealing that could compromise sterility. The recall affects units distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, SINGLE SHOT EPIDURAL, Item No.570-3089
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0522-2023·2022-12-21
Surgical Procedure Trays Recalled for Incomplete Sterile Barrier Sealing
Stradis Medical recalls Henry Schein surgical procedure trays due to incomplete outer bag sealing that may compromise sterility. No injuries reported.
Product
HENRY SCHEIN, LOOP RECORDER PACK, Item No.570-2891
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0487-2023·2022-12-21
Oral Surgery Trays Recalled for Incomplete Sealing of Sterility Bags
Stradis Healthcare is recalling certain oral surgery trays because the outer packaging may be incompletely sealed, potentially compromising the sterility of the surgical instruments.
Product
STRADIS HEALTHCARE, Surg, Item No.40551TMS. oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0514-2023·2022-12-21
ENT Surgical Kits Recalled for Potential Sterility Loss
Stradis Medical is recalling HENRY SCHEIN ENT surgical kits distributed nationwide due to defective outer bag sealing that may compromise sterility. Affected kits were distributed across the US and Canada.
Product
HENRY SCHEIN, ENT SET UP PACK, Item No.570-2742
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0717-2023·2022-12-21
Diagnostic Kit Recall: Falsely Elevated Mold Allergen Test Results
Siemens IMMULITE 2000 allergen testing kits may produce falsely elevated results for mold allergen-specific IgE, potentially leading to incorrect mold allergy diagnoses.
Product
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS, except Japan Siemens Material Number (SMN): 10380875 For the quantitative measurement of allergen-specific IgE in human serum, as an aid in the clinical diagnosis of IgE mediated allergic disorders.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0500-2023·2022-12-21
Stradis Healthcare Introducer Kit Micro recalled for potential sterility compromise
Stradis Healthcare is recalling 180 units of its Introducer Kit Micro cardiovascular devices due to potential incomplete sealing of outer bags that may compromise sterility.
Product
STRADIS HEALTHCARE, Introducer Kit Micro, Item No.525-038, cardiovascular
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0491-2023·2022-12-21
Stradis Healthcare Oral Surgery Trays Recalled Due to Incomplete Sealing
Stradis Healthcare is recalling oral surgery trays due to incomplete outer bag sealing that may compromise the sterility of the surgical kit.
Product
STRADIS HEALTHCARE, pack Item No.40788SMS, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0508-2023·2022-12-21
Surgical Procedure Trays Recalled for Potential Sterility Breach
Stradis Medical recalls surgical procedure trays due to incomplete outer bag sealing that may compromise sterility. The affected products were distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, Basin Set, Item No.570-1803
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2023·2022-12-21
Electrosurgical Suction Coagulator Devices Recalled Due to Potential Suction Port Blockage
ConMed's electrosurgical suction coagulator devices may have blocked suction ports that prevent proper function during procedures. Affected devices could cause procedure delays and require alternative equipment.
Product
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2023·2022-12-21
Henry Schein Universal Tray Recall for Incomplete Sealing
Stradis Medical recalls 675 Henry Schein Universal Trays due to incomplete outer bag sealing that may compromise sterility. The defect affects surgical procedures nationwide and in Canada.
Product
HENRY SCHEIN, UNIVERSAL TRAY, Item No.570-2787
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0507-2023·2022-12-21
Surgical Procedure Trays Recalled for Potential Sterility Breach
Stradis Medical recalls Henry Schein Basin Pack surgical trays due to potentially incomplete outer packaging seals that may compromise sterility of the medical kits.
Product
HENRY SCHEIN, Basin Pack, Item No.570-1692
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0539-2023·2022-12-21
Stradis Ablation Pack Recalled for Potentially Compromised Sterile Seal
Stradis Healthcare is recalling Ablation Pack Item No. 682-130 due to incomplete outer bag seals that may compromise sterility. The defect may allow contamination of surgical kits.
Product
STRADIS HEALTHCARE, Ablation Pack, Item No.682-130,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0552-2023·2022-12-21
Surgical Procedure Kits Recalled for Incomplete Outer Bag Seal
Stradis Healthcare is recalling Varicosity Basic Pack surgical procedure kits (105 units) distributed in the US and Canada due to potentially incomplete outer bag sealing that may compromise sterility.
Product
STRADIS HEALTHCARE, Varicosity Basic Pack, Item No.682-947,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0545-2023·2022-12-21
Stradis Healthcare Vein RF Pack surgical trays recalled for incomplete outer bag seal
Stradis Healthcare is recalling 400 units of Vein RF Pack surgical trays due to manufacturing defects that may result in incomplete outer bag sealing, potentially compromising sterility.
Product
STRADIS HEALTHCARE, Vein RF Pack, Item No.682-1942NL1,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0518-2023·2022-12-21
Medical Procedure Trays Recalled for Potential Sterility Breach
Stradis Healthcare is recalling 100 units of Henry Schein CATH PACK kits due to manufacturing defects that may leave outer bags incompletely sealed, potentially compromising sterility.
Product
HENRY SCHEIN, CATH PACK Item No.570-2789
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0526-2023·2022-12-21
Surgical procedure kit recalled due to incompletely sealed outer bag
A HENRY SCHEIN extremity pack surgical kit is being recalled because its outer bag may not be completely sealed, which could compromise the sterility of the kit. Affected units were distributed nationwide in the US and Canada.
Product
HENRY SCHEIN, EXTREMITY PACK, Item No.570-2946
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0554-2023·2022-12-21
Angio Pack surgical trays recalled for incomplete sealing and sterility breach
Stradis Healthcare is recalling Angio Pack surgical trays due to manufacturing defects that may leave the outer bag incompletely sealed, compromising product sterility. Affected units were distributed nationwide in the US and Canada.
Product
STRADIS HEALTHCARE, Angio Pack, Item No.686-199,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0718-2023·2022-12-21
Siemens allergy test kits recalled for false mold allergen reactivity results
Siemens Healthcare Diagnostics is recalling 560 allergy diagnostic kits (Lot 565) due to potential for falsely elevated mold allergen reactivity, which may result in incorrect test results.
Product
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan Siemens Material Number (SMN): 10711939 For the quantitative measurement of allergen-specific IgE in human serum, as an aid in the clinical diagnosis of IgE mediated allergic disorders.
Category
Medical Device
Distribution
Distributed nationwide