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.

8726–8750 of 84715

SevereFDA (Food)·F-0358-2025·2025-01-08
Organic Baby Carrots Recalled Due to E. coli Contamination Risk
Grimmway Farms is recalling organic baby carrots sold under multiple brands due to potential E. coli O121:H19 contamination affecting approximately 218,705 cases distributed nationwide and internationally.
Product
--- Organic Baby Carrots --- Orangic Baby Peeled Carrots 13/3 BL; Orangic Baby Peeled Carrots 30/1 BL; Org Baby Peeled Carrots 12/2 Wholesome Pantry RPC; Org Baby Peeled Carrots 24/1 Wholesome Pantry RPC; Organic Baby Peeled Carrots 10/2/2Lb Cal O Display; Organic Baby Peeled Car
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0357-2025·2025-01-08
Organic Baby Carrots Recalled for E. coli O121:H19 Contamination
Grimmway Farms is recalling organic baby carrots (Cal-Organic and Marketside brands) due to potential E. coli O121:H19 contamination affecting 10,482 cases distributed across the U.S., Puerto Rico, and internationally.
Product
--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz Steam-to-Serve RPC --- Brand --- Cal-Organic; Marketside
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0359-2025·2025-01-08
Grimmway Farms Organic Baby Carrots recalled for E. coli O121 contamination
Grimmway Farms is recalling approximately 21,094 cases of Organic Baby Carrots that may be contaminated with E. coli O121:H19. The product was distributed across 38 U.S. states, Puerto Rico, and Canada, UAE, Hong Kong, and Colombia.
Product
--- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms; Organic Baby Carrots 25 Lbs. Grimmway Farms --- Brand --- Grimmway Farms
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0360-2025·2025-01-08
Organic Carrots Recalled Due to Potential E. coli O121:H19 Contamination
Grimmway Enterprises is recalling organic whole and juice carrots sold under multiple brands due to potential contamination with E. coli O121:H19. The recall affects carrots distributed across the U.S., territories, and certain foreign countries.
Product
--- Organic Whole Carrots --- Organic Carrot 125/6 Cal-Organic Farms; Organic Carrot 150/5 Bunny Luv; Organic Carrots 10/5 Lb O-Organic; Organic Carrots 10/5 Simple Truth; Organic Carrots 10/5# 365 Organic; Organic Carrots 10/5# 365 Organic RPC; Organic Carrots 10/5# Bunny Luv;
Category
Food
Distribution
41 states
SevereFDA (Drugs)·D-0170-2025·2025-01-08
FORCE FOREVER supplement tablets recalled for undisclosed drugs
GNMart LLC is recalling FORCE FOREVER 400mg tablets nationwide after the FDA found the product contains undisclosed Diclofenac and Dexamethasone. The Class I recall affects all lots of this dietary supplement product.
Product
FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0363-2025·2025-01-08
Gyro Kit with Trays recalled due to Salmonella in tzatziki sauce
Reser's Fine Foods is recalling its Gyro Kit With Trays due to Salmonella contamination in the tzatziki sauce. 705 cases were distributed to food service establishments across 19 states.
Product
FCF Item 404884, Gyro Kit With Trays. Each tray consists of 2/5.25lbs. packages. UPC 0 13454 38155. Distributed by Fresh Creative Foods, Vista CA. Each kit consists of 8 bags of Traditional Pita Bread, 2/32oz. bags of Gyro Slices, 2 Sleeves of 4/2oz. cups premium Tzatziki sauce
Category
Food
Distribution
19 states
SevereFDA (Food)·F-0361-2025·2025-01-08
Organic Whole Carrots Recalled for Potential E. coli O121:H19 Contamination
Grimmway Farms is recalling approximately 4,057 cases of organic whole carrots distributed nationally due to potential E. coli O121:H19 contamination. No illnesses have been reported.
Product
--- Organic Whole Carrots --- Organic Clip Carrots 50 Lbs Cal-Organic Farm; Organic Clip Carrots 50 Lbs Cal-Organic RPC --- Brand --- Cal-Organic
Category
Food
Distribution
41 states
HighFDA (Devices)·Z-0784-2025·2025-01-08
Medline Custom Surgical Procedure Kits Recalled for Potential Endotoxin Contamination
Medline Industries is recalling custom medical procedure kits due to non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 1,072 units were distributed in the US, Canada, and UAE.
Product
Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE, REF DYNJ58648B; 2) ENDOSCOPIC SKULL BASE, REF DYNJ58648C; 3) ENT ENDO SINUS WILMINGTON PACK, REF DYNJ66447; 4) ENDOSCOPIC SKULL BASE, REF DYNJ58648D; 5) ENDOSCOPIC SKULL BASE, REF DYNJ58648J.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0783-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling 943 custom surgical kits containing non-sterile Codman Surgical Patties and Strips that may be contaminated with endotoxin.
Product
Medline custom medical procedure kits labeled as: 1) FREE FLAP BASIC SET-UP PK, REF DYNJ0991320J; 2) MVFF/FIBU #54-RF, REF DYNJ21927R; 3) FUNCTIONAL SINUS ENDOSCOPY, REF DYNJ40406A; 4) DR GOLDSTEIN ACCESSORY PACK, REF DYNJ51818F; 5) ENDOSCOPIC SKULL BASE, REF DYNJ58648
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0792-2025·2025-01-08
Medline Medical Procedure Kits Recalled for Non-Sterile Component Contamination
Medline Industries is recalling 2,664 custom medical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The affected kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0167-2025·2025-01-08
Levothyroxine Sodium tablets recalled for impurity specification failure
Lupin Pharmaceuticals is recalling Levothyroxine Sodium 75 mcg tablets due to out-of-specification impurities detected in stability testing. Affected lot LA01276 (expiring 07/2026) was distributed to one Ohio distributor.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
1 state
HighFDA (Devices)·Z-0791-2025·2025-01-08
Medline Deep Brain Stimulation Surgical Kits Recalled for Non-Sterile Contamination
Medline has recalled 128 Deep Brain Stimulation surgical kits for containing non-sterile Surgical Patties and Strips with potential endotoxin contamination. Affected units were distributed worldwide including the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION PACK-LF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0793-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components
Medline is recalling 182 custom surgical procedure kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF, REF DYNJ0867145G; 2) CERVICAL SPINE PACK HUM-LF, REF DYNJ35184F; 3) ANTERIOR CERVICAL-CORPECTOMY, REF DYNJ904827.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0790-2025·2025-01-08
See DocMan Surgical Kits Recalled for Non-Sterile Surgical Patties and Strips
Medline Industries is recalling See DocMan custom convenience kits containing non-sterile Codman Surgical Patties and Strips due to potential endotoxin contamination.
Product
See DocMan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0789-2025·2025-01-08
Medline MICRODISECTOMY PACK recalled for endotoxin contamination
Medline custom MICRODISECTOMY PACK kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination are being recalled. Approximately 1,494 units were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK, REF DYNJ80585A; 2) MICRODISECTOMY PACK, REF DYNJ80585B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0797-2025·2025-01-08
3M Unitek Orthodontic Primer Recalled Due to Bond Failures and Skin Irritation
3M Unitek is recalling Transbond Plus Self-Etching Primer used in orthodontic bonding due to reports of bracket bond failures and skin irritation or blistering.
Product
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self Etching Primer is an orthodontic all-in-one etchant and primer that is used in the bonding process of orthodontic appliances to teeth.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0779-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling custom surgical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The recall affects 1,402 units distributed in the US, Canada, and UAE.
Product
Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF, REF DYNJ0713177; 3) BURR HOLE SHUNT PACK, REF DYNJ56819D; 4) BURR HOLE SHUNT PACK, REF DYNJ56819F; 5) BURR HOLE SHUNT PACK, REF DYNJ56819G; 6) RO VP SH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0782-2025·2025-01-08
Medical Device Kits Recalled for Non-Sterile Surgical Components
Medline Industries is recalling See DocMan custom convenience kits that contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 48,655 units were distributed worldwide.
Product
See DocMan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0773-2025·2025-01-08
Medtronic Implantable Drug Pumps Recalled for Software Defects
Medtronic has recalled 566 SynchroMed II and III implantable drug infusion pumps due to software issues in the controlling application. No injuries or illnesses have been reported.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0172-2025·2025-01-08
Dapsone Topical Gel Recalled Due to Crystallization Defect
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% (2760 packs) distributed nationwide due to crystallization in the formulation. The voluntary recall affects lots T400514 and T400808.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0772-2025·2025-01-08
SynchroMed II and III implantable pumps recalled for software issues
Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0174-2025·2025-01-08
Injectable phenylephrine recalled due to defective tamper-evident seals nationwide
Hikma Injectables is recalling phenylephrine injections nationwide because tamper-evident seals on some syringes were not properly attached. Affected lot 243120003D has a use-by date of 03/11/2025.
Product
phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0785-2025·2025-01-08
Medline surgical procedure kits recalled for potential endotoxin contamination
Medline is recalling three custom surgical procedure kits due to non-sterile Codman Surgical Patties and Strips that pose a potential endotoxin contamination risk. The affected kits were distributed in the US, Canada, and the UAE.
Product
Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK, REF DYNJ66449.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk
Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0777-2025·2025-01-08
Medline surgical procedure kits recalled for non-sterile supplies
Medline is recalling custom medical procedure kits containing non-sterile surgical supplies with potential endotoxin contamination. The affected kits were distributed nationwide and internationally.
Product
Medline custom medical procedure kits labeled as: 1) CATH LAB PACK-LF, REF DYNJ0382559M; 2) CRANI, REF DYNJ56001B; 3) GENDER AFFIRMING SURGERY, REF DYNJ66252; 4) GENDER AFFIRMING SURGERY, REF DYNJ66252A; 5) MAJOR NEURO PACK-LF, REF DYNJ0578916X.
Category
Medical Device
Distribution
Distributed nationwide