State

Ohio product recalls

73,584 recalls have nationwide distribution and so reach Ohio. 11,764 additional recalls listed Ohio specifically in their distribution scope.

What the numbers show

Total: 11,764
Critical: 2,117
Severe: 2,903
Most recent: 2026-10-21

Of the 11,764 recalls naming Ohio we have scored against our rubric, 2,117 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,903 (25%) are Severe.

Which agencies issued them

These figures cover only the 11,764 recalls whose distribution notice names Ohio specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

151–175 of 85348

SevereFDA (Drugs)·D-0023-2027·2026-10-14
FDA Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0085-2027·2026-10-14
Stryker Bard EP XT Decapolar Steerable Diagnostic EP Catheter Recalled for Sterile Barrier Breach
Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation.
Product
BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0017-2027·2026-10-14
biQ-FEL Beverage Recalled for Undeclared Sildenafil and Tadalafil
A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.
Product
biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA COLOMBIANA; Distributed by: Biofel
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0031-2027·2026-10-14
Carolina Infusion Recalls Tri-MIX Injectable Due to Sterility Concerns
Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.
Product
Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0024-2027·2026-10-14
Saint Francis Apizza Frozen Supreme Pizza Recalled for Undeclared Soy
Saint Francis Apizza LLC is recalling 1,920 units of Frozen Supreme Pizza due to undeclared soybean oil and soy lecithin. The product was distributed in Kentucky and Ohio.
Product
Saint Francis Apizza Frozen Supreme Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27760 7
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0021-2027·2026-10-14
FDA recalls injectable compounded mixture in single-use syringes
Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.
Product
QUAD-MIX( PAPAV/PHENTO/ALPROS/TROP) INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0078-2027·2026-10-14
Philips Spectral CT Systems Recalled for Software Issues Affecting Safety
Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.
Product
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model Numbers: 1. 728333 (U.S. and Outside U.S.), 2. 728340 (Outside U.S.), 3. 728344 (Outside U.S.), 4. 728345 (Outside U.S.);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0022-2027·2026-10-14
Saint Francis Apizza Frozen Cheese Pizza Recalled for Undeclared Soy
Saint Francis Apizza LLC is recalling 4,255 units of frozen cheese pizza due to undeclared soy ingredients. The product was distributed in Kentucky and Ohio.
Product
Saint Francis Apizza Frozen Cheese Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27759 1
Category
Food
Distribution
2 states
HighFDA (Food)·H-0023-2027·2026-10-14
Saint Francis Apizza Frozen Mushroom and Onion Pizza Recalled for Undeclared Soy
Saint Francis Apizza LLC is recalling 2,655 units of frozen Mushroom & Onion Pizza in Kentucky and Ohio due to undeclared soy ingredients.
Product
Saint Francis Apizza Frozen Mushroom & Onion Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27764 5
Category
Food
Distribution
2 states
HighFDA (Food)·H-0021-2027·2026-10-14
Saint Francis Apizza Frozen Pepperoni Pizza Recalled for Undeclared Soy
Saint Francis Apizza LLC is recalling 4,931 units of frozen pepperoni pizza due to undeclared soybean oil and soy lecithin.
Product
Saint Francis Apizza Frozen Pepperoni Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic, UPC: 6 66186 27762 1
Category
Food
Distribution
2 states
HighNHTSA·26V674000·2026-10-14
PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Bunk Restraint Defect
PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.
Product
KENWORTH — KENWORTH, PETERBILT T680, W900, 579, 589
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0073-2027·2026-10-14
Steris VERIFY Dual Species Biological Indicator Recall for Spore Population Issues
Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.
Product
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·N/A·2026-10-14
Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.
Product
Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0101-2027·2026-10-14
Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination
Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.
Product
DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0090-2027·2026-10-14
Onkos My3D Personalized Pelvic Implant Recalled for Distribution Error
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Product
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0095-2027·2026-10-14
AVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination
AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.
Product
ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0103-2027·2026-10-14
AVID Medical Recalls Urology Kits for Potential Lubricant Contamination
AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.
Product
UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0082-2027·2026-10-14
DRG Sperm Ab ELISA Recalled for Potential False Negative Results
DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries.
Product
Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0013-2027·2026-10-14
Preferred Pharmaceuticals Recalls Lidocaine Ointment Due to Content Uniformity Failures
Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide.
Product
Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro Pharmaceuticals U.S.A., Inc., Prod# (NDC): 68788-7865-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0007-2027·2026-10-14
Mezzetta Golden Greek Peperoncini Recalled for Potential Mouse Contamination
G L Mezzetta Inc is recalling 32 fl oz jars of Golden Greek Peperoncini Medium Heat due to potential contamination with mice.
Product
Mezzetta GOLDEN GREEK PEPERONCINI MEDIUM HEAT 32 FL OZ G.L. MEZZETTA, INC., AMERICAN CANYON, NAPA VALLEY, CA 94503 PRODUCT OF GREECE UPC: 073214003280
Category
Food
Distribution
22 states
ModerateFDA (Devices)·Z-0102-2027·2026-10-14
AVID Medical Recalls Heart Prep Trays for Lubricant Contamination
AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.
Product
HEART PREP TRAY; Model/Item Number (Kit): MECV97W;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0091-2027·2026-10-14
Onkos Surgical Recalls My3D Personalized Pelvic Implant Due to Distribution Error
Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.
Product
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0014-2027·2026-10-14
Cipla Recalls Fosfomycin Tromethamine Due to Impurity Specification Failures
Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications.
Product
FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0077-2027·2026-10-14
Halyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
GRI Medical is recalling Halyard Laparoscopy Comprehensive Pack II kits because they contain a latex urethral catheter despite being labeled as latex-free.
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0100-2027·2026-10-14
AVID Medical Recalls Plastic Trays Due to Lubricant Contamination
AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.
Product
PLASTICS TRAY; Model/Item Number (Kit): EURO053;
Category
Medical Device
Distribution
Distributed nationwide