State

Ohio product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8526–8550 of 84715

SevereFDA (Devices)·Z-0822-2025·2025-01-22
ACCOLADE DR Pacemakers Recalled for Unintended Safety Mode Activation
Boston Scientific is recalling ACCOLADE DR Pacemakers built before September 2018 due to risk of unintended Safety Mode activation caused by battery impedance issues. The devices may enter Safety Mode during normal telemetry operations.
Product
ACCOLADE DR Pacemaker, SL (Model Number L301), SL MRI (Model Number L311), EL (Model Number L321), and EL MRI (Model Number L331)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0824-2025·2025-01-22
ESSENTIO DR Pacemakers May Malfunction Due to Battery Impedance Issue
Boston Scientific is recalling certain ESSENTIO DR Pacemakers manufactured before September 2018 due to latent battery impedance that may cause Safety Mode malfunction during normal operations.
Product
ESSENTIO DR Pacemaker, SL (Model Number L101, SL MRI (Model Number L111), EL (Model Number L121), and EL MRI (Model Number L131)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0764-2025·2025-01-22
Medline Fluid Delivery Sets incorrectly assembled with wrong drip chamber
Medline fluid delivery sets were assembled with a macro drip chamber instead of the required micro drip chamber, delivering three times more fluid per drop and risking patient fluid overload.
Product
Medline Fluid Delivery Set with Drip Chamber: 1) FDS,135,CHMN,W/F,MLL,RC(2),PG, Item Number 99000069; 2) FDS,135,NV,MICRO-CHAMBER,W/FILTER,BLUE, Item Number 949000222; 3) FDS,135,NV,MICRO-CHAMBER,W/FILTER,GREEN, Item Number 949000224; 4) FDS,135,NV,MICRO-CHAMBER,W/FILTER,RE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0885-2025·2025-01-22
Welch Allyn Life2000 Ventilator Battery Charger May Cause Device Inoperability
Baxter Healthcare is recalling 946 Welch Allyn Life2000 ventilators due to a battery charger defect that can trigger an alarm and render the device inoperable.
Product
Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0886-2025·2025-01-22
Welch Allyn Life2000 Ventilator Battery Charger Malfunction Recall
Baxter Healthcare Corporation is recalling Welch Allyn Life2000 Ventilation Systems due to a battery charger malfunction that triggers an alarm and renders the ventilator inoperable.
Product
Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002AP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0426-2025·2025-01-22
Wicklow Gold Cheddar Cheese Recalled for Potential Listeria Contamination
Abbey Specialty Foods is recalling Wicklow Gold Cheddar Tomato & Herb cheese distributed in Massachusetts, Colorado, and Ohio due to potential Listeria monocytogenes contamination.
Product
Wicklow Gold Cheddar Tomato & Herb, 5.2 oz., plastic cryo-vac , 8 packages per case
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-0765-2025·2025-01-22
Medline Fluid Delivery Sets Recalled Due to Assembly Error
Medline Fluid Delivery Sets were incorrectly assembled with macro drip chambers instead of required micro drip chambers. The macro chamber delivers three times more fluid per drop, creating a risk of dosing errors.
Product
Medline Fluid Delivery Set with Drip Chamber: 1) MTO,135,YELLOW,MICRO,SPK-MAIMONIDES, Item Number: 60130527; 2) MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH, Item Number: 65111341; 3) MTO,ANGIO,SINGLE,SPIKE,KIT, Item Number: 65232486; 4) MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM, Item
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0935-2025·2025-01-22
Sklar Instruments Recalls Sterile Vein Hooks Due to Packaging Issues
Sklar Instruments is recalling 1,050 units of ECONO STERILE Vein Hooks due to packaging issues that may breach the sterile barrier. Products were distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE VEIN HOOK 1.5MM STERILE CS/25, Model Number 96-4020M; 2) ECONO STERILE VEIN HOOK 2MM STERILE CS/25, Model Number 96-4021M; 3) ECONO STERILE VEIN HOOK 2.5MM STERILE CS/25, Model Number 96-4022M; venous proced
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0856-2025·2025-01-22
8MM Maryland Bipolar Forceps Recalled Due to Frayed Grip Cables
Intuitive Surgical is recalling 8MM Maryland Bipolar Forceps due to increased complaints about frayed or broken grip cables on these reusable surgical instruments. Approximately 7,132 units have been distributed.
Product
8MM,MARYLAND BIPOLAR FORCEPS,IS4000 ¿ REF 470172
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0863-2025·2025-01-22
8MM Dual Blade Retractors recalled for frayed or broken grip cables
Intuitive Surgical is recalling 8MM Dual Blade Retractors due to increased complaints of frayed or broken grip cables. This defect affects 783 reusable surgical instruments distributed in the U.S. and internationally.
Product
8MM,DUAL BLADE RETRACTOR,IS4000¿ REF 470249
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0937-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Surgical Scalpel Handles for Sterile Barrier Risk
Sklar Instruments recalls ECONO STERILE SCALPEL HDL #3 surgical handles due to packaging issues that may compromise the sterile barrier. The 150-unit recall affects units distributed nationwide with lot code SK-125.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCALPEL HDL #3 W/METRIC CS/25, Model Number 96-3500M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0854-2025·2025-01-22
Prograsp Surgical Forceps Recalled Due to Frayed Grip Cables
Intuitive Surgical is recalling 2,852 units of 8MM Prograsp Forceps due to complaints of frayed or broken grip cables. These reusable surgical instruments may lose grip control during use.
Product
8MM,PROGRASP FORCEPS,IS4000 ¿ REF 470093
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0857-2025·2025-01-22
Surgical Forceps Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling 373 Resano Forceps due to increased complaints of frayed or broken grip cables on the reusable surgical instruments. Affected healthcare providers should contact the manufacturer for guidance.
Product
8MM,RESANO FORCEPS,IS4000 ¿ REF 470181
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0912-2025·2025-01-22
Cardinal Health Laryngoscopy Presource Kits Recalled for Endotoxin Contamination
Cardinal Health is recalling 512,786 Laryngoscopy Presource Kits due to potential endotoxin contamination in non-sterile surgical strips and patties. The kits were distributed to the United States, Canada, and Saudi Arabia.
Product
Cardinal Health Presource Kits: 1 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH2 ; 2 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH3 ; 3 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH4 ; 4 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH5 ; 5 ) STERILE LARYNGOSCOPY PACK, Cata
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0851-2025·2025-01-22
Intuitive Surgical Micro Forceps Recalled Due to Grip Cable Defects
Intuitive Surgical is recalling 8MM Black Diamond Micro Forceps (Model 470033) due to complaints of frayed or broken grip cables. The defect affects 1,111 units distributed nationwide and internationally.
Product
8MM,BLACK DIAMOND MICRO FORCEPS,IS4000 ¿ REF 470033
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0860-2025·2025-01-22
Intuitive Surgical Tenaculum Forceps Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling 11,162 units of 8MM Tenaculum Forceps (Model 470207) due to increased complaints of frayed or broken grip cables on reusable surgical instruments. Users should discontinue use immediately.
Product
8MM,TENACULUM FORCEPS,IS4000¿ REF 470207
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0934-2025·2025-01-22
ECONO STERILE Dental Cement Spatula Kits Recalled for Packaging Issues
Sklar Instruments is recalling ECONO STERILE dental cement spatulas (Model 96-2245M) due to packaging defects that may compromise the sterile barrier. The product was distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE CEMENT SPATULA #24 STRL CS/25, Model Number 96-2245M, mixing utensil, dental
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0201-2025·2025-01-22
Clobazam tablets recalled for contamination with foreign tablets
Amerisource Health Services LLC is recalling Clobazam 10 mg tablets nationwide due to contamination with foreign tablets or capsules. Patients should contact their pharmacist or healthcare provider.
Product
CLOBAZAM — CLOBAZAM (CLOBAZAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0883-2025·2025-01-22
Intuitive Surgical recalls 8MM Force Bipolar surgical instruments due to grip cable failures
Intuitive Surgical is recalling approximately 46,759 8MM Force Bipolar IS4000 surgical instruments nationwide and internationally due to reports of frayed or broken grip cables that could compromise instrument function during surgical use.
Product
8MM,FORCE BIPOLAR,IS4000 REF 471405
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0844-2025·2025-01-22
Folysil Silicone Foley Catheters Recalled for Possible Sterility Issue
Coloplast recalls Folysil Silicone Foley Catheters due to a possible sterility defect detected at the manufacturing facility. The affected units may not maintain proper sterilization, posing a risk of infection.
Product
Folysil Silicone Foley Catheters, Device Reference Numbers AA6106, AA6108, AA6110, AA6112, AA6114, AA6116, AA6118, AA6120, AA6122, AA6124, AA6308, AA6310, AA6312, AA6314, AA6316, AA6318, AA6320, AA6322, AA6324, AA6408, AA6410, AA6412, AA6414, AA6416, AA6418, AA6420, AA6422, AA642
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0909-2025·2025-01-22
Surgical Kit Recall: Potential Endotoxin Contamination in Cardinal Health Presource Kits
Cardinal Health recalls Presource surgical kits due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected units were distributed in the US, Canada, and Saudi Arabia.
Product
Cardinal Health Presource Kits: 1 ) TRIPLE ENDO PACK, Catalog Number: SBAOCTEHH1:; 2 ) TRIPLE ENDO PACK, Catalog Number: SBAOCTEHHA:; 3 ) RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERM5:; 4 ) RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERMO:; 5 ) RIVERSIDE S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0904-2025·2025-01-22
Medtronic NanoCross Elite PTA Catheter Recall Due to Balloon Deflation
Medtronic's NanoCross Elite PTA catheters in certain lots may not deflate properly during use. The FDA is recalling 5,189 units due to potential in-vivo balloon deflation issues.
Product
Medtronic NanoCross Elite PTA catheter, REF numbers amd sizes: 1) AB14W050020090, Size: 5MM X 20MM X 90CM; 2) AB14W050020150, Size: 5MM X 20MM X 150CM; 3) AB14W050040090, Size: 5MM X 40MM X 90CM; 4) AB14W050040150, Size: 5MM X 40MM X 150CM; 5) AB14W050060150,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0876-2025·2025-01-22
8MM Maryland Bipolar Forceps Recalled for Frayed Grip Cable
Intuitive Surgical is recalling 68,458 units of its 8MM Maryland Bipolar Forceps due to increased complaints about frayed or broken grip cables on the reusable surgical instruments.
Product
8MM,MARYLAND BIPOLAR FORCEPS,IS4000 REF 471172
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0950-2025·2025-01-22
Strabismus Surgical Scissors Kits Recalled Due to Sterile Barrier Packaging Issues
Sklar Instruments is recalling 350 strabismus surgical scissors kits nationwide due to packaging issues that may compromise the sterile barrier.
Product
Medical procedure kits labeled as: 1) ECONO STERILE STRABIS SCISS STR 4.5"STER 50, Model Number 96-2540; 2) ECONO STERILE STRABIS SCISS CVD 4.5"STER 50, Model Number 96-2541; 3) ECONO STERILE STRABIS SCISS STR 4.5"STER 25, Model Number 96-2542; 4) ECONO STERILE STRABISM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0938-2025·2025-01-22
Surgical Suction Tubes Recalled for Sterile Packaging Defects
ECONO STERILE suction tubes and surgical instruments (150 units, nationwide) are recalled for packaging defects that may breach the sterile barrier and create infection risk during medical procedures.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE YANKAUER SUCTION TUBE 8.5" C10, Model Number 96-4176; 2) ECONO STERILE YANKAUER SUCTION TUBE 11" CS10, Model Number 96-4177; 3) ECONO STERILE FRAZIER TUBE 6FR STERILE CS/25, Model Number 96-5434; 4) ECONO
Category
Medical Device
Distribution
Distributed nationwide