The Recall Desk

State

Ohio product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26126–26150 of 85340

  • ModerateFDA (Drugs)·D-0025-2022·2021-10-27

    AirDuo Digihaler 232/14 Inhalation Powder Recall for Subpotent Salmeterol

    Teva Pharmaceuticals is recalling approximately 5,500 units of AirDuo Digihaler 232/14 inhalation powder distributed nationwide because some inhalers contain less salmeterol than the labeled dose.

    Product
    AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-136-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0143-2022·2021-10-27

    Smith & Nephew cannulated screw label incorrectly indicates threading type

    Smith & Nephew is recalling 6.5mm x 165mm cannulated screws because the product label incorrectly states the screws are fully threaded when they are actually partially threaded.

    Product
    6.5MMX165MM CANNULATED SCREW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0017-2022·2021-10-27

    Coppertone Pure & Simple Baby 50 Sunscreen Spray Recalled for cGMP Deviations

    Beiersdorf Inc. is recalling 14,748 cans of Coppertone Pure & Simple baby 50 Sunscreen Spray due to cGMP (current Good Manufacturing Practice) deviations. The product was distributed nationwide.

    Product
    Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0026-2022·2021-10-27

    Omeprazole Magnesium Acid Reducer Capsules Recalled for Staple Contamination

    Dr. Reddy's Laboratories is recalling Acid Reducer (Omeprazole Magnesium) 20 mg capsules nationwide because staples have been found co-mingled with capsules in bottles.

    Product
    ACID REDUCER — ACID REDUCER (OMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0024-2022·2021-10-27

    AirDuo Digihaler inhalation powder subpotent drug recall

    Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some batches do not deliver the labeled amount of salmeterol, a critical active ingredient for asthma and COPD control.

    Product
    AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0151-2022·2021-10-27

    HemosIL Liquid Anti-Xa Assay On-Board Stability Issue Recall

    Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa, a coagulation assay measuring heparin activity, due to reduced on-board instrument stability from 7 days to 5 days.

    Product
    HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0154-2022·2021-10-27

    Jamshidi Bone Marrow Biopsy Tray Recalled Due to Misbranding

    Bard Peripheral Vascular Inc. is recalling 360 Jamshidi Bone Marrow Biopsy Trays (Catalog # BEK3411, Lot # 0001378561) due to misbranded labeling. The FDA classified this as a Class II recall affecting healthcare facilities in 16 U.S. states and Puerto Rico.

    Product
    Catalog # BEK3411, Ecomomy Jamshidi Bone Marrow Biopsy Tray, 11 G X 4"Biopsy/Aspiration needle, sterile, Qty: 10, Single Use Only, RX only. Exp. Date Lidocaine Vendor lot. CareFusion Intended use to aspirate marrow from either the sternum or the iliac crest. Intraosseous…
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0149-2022·2021-10-27

    Heparin Activity Assay Labeling Correction: Reduced On-Board Stability

    Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa kits due to a labeling correction. The on-board stability window has been reduced from 7 to 5 days.

    Product
    HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACL TOP¿ Family, ACL TOP Family 50 Seriest and ACL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0126-2022·2021-10-27

    Plastic Tenaculum Surgical Instruments Recalled for Unconfirmed Manufacturing Standards

    Stradis Medical is recalling plastic tenaculum surgical instruments because the manufacturer cannot confirm they were produced in accordance with required design and manufacturing standards. Approximately 2,483 kits were distributed nationwide and to Canada.

    Product
    Tenaculum, Plastic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0021-2022·2021-10-27

    AirDuo Digihaler 113/14 Inhalation Powder Subpotent Drug Recall

    Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some units contain less salmeterol than the labeled dose. The affected sample batch was distributed nationwide.

    Product
    AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC , Frazer, PA 19355, Manufactured in Ireland, NDC 59310-520-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0027-2022·2021-10-27

    Lupin Imipramine Pamoate Capsules Recalled for Failed Dissolution Test

    Lupin Pharmaceuticals is recalling approximately 1,902 bottles of Imipramine Pamoate Capsules 125 mg due to out-of-specification results in dissolution testing at the 9-month stability checkpoint.

    Product
    IMIPRAMINE PAMOATE — IMIPRAMINE PAMOATE (IMIPRAMINE PAMOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0016-2022·2021-10-27

    Coppertone Pure & Simple Kids 50 Sunscreen Spray Recalled for cGMP Deviations

    Beiersdorf Inc. is voluntarily recalling Coppertone Pure & Simple kids 50 Sunscreen Spray due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 70,320 cans distributed nationwide.

    Product
    Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·22008·2021-10-27

    5.11 Tactec Plate Carriers Recalled Due to Injury Hazard

    5.11 Inc. is recalling about 45,170 Tactec Plate Carriers (style 56100) because the cable in the quick release system can separate from the handle, preventing swift removal in an emergency. No injuries have been reported.

    Product
    56100 Tactec™ Plate Carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0020-2022·2021-10-27

    GlipiZIDE Extended-Release Tablets 2.5 mg Nationwide Recall

    American Health Packaging is recalling GlipiZIDE Extended-Release Tablets 2.5 mg (Lot #194141) nationwide because dissolution test results exceeded specification, which may affect the drug's effectiveness.

    Product
    GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E090000·2021-10-26

    WABCO Trailer ABS Systems Recalled for Brake Pressure Loss Risk

    WABCO is recalling certain Trailer ABS Systems because improperly tightened screws may loosen, causing pressure loss and potential brake failure.

    Product
    SERVICE BRAKES, AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V837000·2021-10-25

    2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk

    Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V835000·2021-10-25

    Tesla Model 3 and Model Y suspension fasteners recalled for loosening

    Tesla is recalling 2019-2021 Model 3 and 2020-2021 Model Y vehicles where front suspension lateral link fasteners may loosen, potentially causing wheel misalignment and increasing crash risk.

    Product
    TESLA — TESLA MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V834000·2021-10-25

    2020-2023 Tesla Model 3 Curtain Airbag Deployment Safety Defect

    Tesla is recalling certain 2020-2023 Model 3 vehicles because the side curtain airbag may be improperly secured to the roof rail and could twist, deploying incorrectly during a crash and increasing risk of injury or ejection.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V836000·2021-10-25

    Yamaha Recalls 2021 Tracer 9 GT for Incorrect VIN Label

    Yamaha is recalling 2021 Tracer 9 GT motorcycles because the VIN on the certification label may not match the vehicle's stamped VIN, potentially preventing owners from receiving safety recall remedies.

    Product
    YAMAHA — YAMAHA TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V833000·2021-10-23

    Ferrari Recalls 458 and 488 Models for Brake Fluid Leak Risk

    Ferrari is recalling specific 458 and 488 models because the brake system may leak fluid, potentially causing a loss of braking ability.

    Product
    FERRARI — FERRARI 488 GTB, 458 ITALIA, 488 SPIDER, 458 SPECIALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·22007·2021-10-22

    Walmart Better Homes and Gardens Room Spray Recalled for Dangerous Bacteria

    Walmart is recalling Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones due to contamination with Burkholderia pseudomallei bacteria. CDC testing identified the hazard and is investigating a cluster of four melioidosis cases, including two deaths.

    Product
    Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V830000·2021-10-22

    2021-2022 Forest River XLR Toy Hauler Recalled for Missing Furnace Protective Panel

    Forest River is recalling certain 2021-2022 XLR Toy Hauler recreational vehicles with a missing protective panel between the furnace and cargo area. The missing panel could allow cargo to contact furnace wiring, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V828000·2021-10-22

    2022 Coachmen Catalina Travel Trailer Recall for Unsealed Furnace Panel

    Forest River is recalling 2022 Coachmen Catalina travel trailers because an unsealed panel between the furnace and cooktop could cause an inverted flame, increasing fire risk.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide