The Recall Desk

State

Oklahoma product recalls

73,366 recalls have nationwide distribution and so reach Oklahoma. 5,816 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,816
Critical
1,043
Severe
1,490
Most recent
2026-09-23

Of the 5,816 recalls naming Oklahoma we have scored against our rubric, 1,043 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,490 (26%) are Severe.

These figures cover only the 5,816 recalls whose distribution notice names Oklahoma specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17501–17525 of 79182

  • HighFDA (Devices)·Z-1434-2023·2023-05-03

    Sterile surgical cardiac catheterization kit recalled for light handle cover separation

    A sterile surgical convenience kit for cardiac catheterization is being recalled because light handle covers may separate and fall off during use. The affected lot includes 322 kits distributed to Florida and Missouri.

    Product
    Sterile surgical convenience kit: regard Item Number: 880393003, HT00997C - Cardiac Cath.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1430-2023·2023-05-03

    Caspar Cervical Retractor Basket Lids Recalled for Incorrect GTIN Labeling

    Aesculap Implant Systems recalls Caspar Cervical Retractor (CCR) Basket lids with incorrect GTIN labeling. The product bears GTIN #04046955299592 instead of the correct #04046955299607.

    Product
    Caspar Cervical Retractor (CCR) Basket ME754 - Lid Only and ME764 Casper Cervical Retractor (CCR) Basket Full System - Lid Only. A lid to a container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments. Note: The CCR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0553-2023·2023-05-03

    Tadalafil Tablets 20 mg recalled due to manufacturing deviations

    Northwind Pharmaceuticals voluntarily recalls Tadalafil 20 mg tablets nationwide due to manufacturing practice deviations. No illnesses have been reported.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0540-2023·2023-05-03

    Pantoprazole Sodium Injection 40 mg Recalled Due to Manufacturing Procedure Deviation

    Methapharm Inc is recalling Pantoprazole Sodium 40 mg injection vials due to a manufacturing procedure deviation. Affected products were inadvertently placed into distribution without proper compliance with approved procedures.

    Product
    Pantoprazole sodium for Injection 40 mg*/vial, Single-dose Vial, Rx only, For Intravenous Infusion Only, Mfd. for Methapharm, Inc. Coral Springs, FL, 33065, NDC 67850-150-10 (carton), NDC 67850-150-00 (vial).
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0544-2023·2023-05-03

    DuPont Recalls Avicel PH-101 Microcrystalline Cellulose for Out-of-Specification Conductivity

    DuPont Nutrition USA is recalling specific batches of Avicel PH-101 NF microcrystalline cellulose due to failed conductivity specifications. The pharmaceutical excipient was distributed in bulk to manufacturers in the USA and multiple international locations.

    Product
    Avicel PH-101 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 50.0 KG / 54.5 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0548-2023·2023-05-03

    Atorvastatin Calcium Tablets Recalled for Manufacturing Quality Violations

    Northwind Pharmaceuticals is recalling 99 bottles of Atorvastatin Calcium 10 mg tablets nationally due to manufacturing process deviations identified in March 2023.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0555-2023·2023-05-03

    FDA recalls Oxytocin product for low potency nationwide

    SCA Pharmaceuticals is recalling Oxytocin 30 units in 0.9% Sodium Chloride solution (73,312 containers) nationwide due to subpotency—product contains insufficient active ingredient.

    Product
    Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor, CT 06095, NDC# 70004-085-44
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0546-2023·2023-05-03

    DuPont Avicel PH-200 NF pharmaceutical ingredient recalled for conductivity specification failure

    DuPont is recalling Avicel PH-200 NF microcrystalline cellulose, a pharmaceutical ingredient, for failing conductivity specifications. The bulk ingredient was distributed to drug manufacturers in the USA and internationally.

    Product
    Avicel PH-200 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0541-2023·2023-05-03

    CBD Metered Dose Inhaler Recalled for Marketing Without FDA Approval

    Wellness BioSciences is recalling its CBD Metered Dose Inhaler nationwide because it was marketed without an approved NDA/ANDA.

    Product
    CBD Metered Dose Inhaler (CBD) 5 mg Dose, 1 Metered Dose Inhaler, 100 Metered Sprays, Wellness BioSciences Rx
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0547-2023·2023-05-03

    DuPont Avicel DG pharmaceutical ingredient recalled for failed quality specification

    DuPont Nutrition USA is recalling Avicel DG, a pharmaceutical ingredient, due to failed quality specifications. The product did not meet conductivity standards during manufacturing testing.

    Product
    Avicel DG, MCC/Dibasic Calcium Phosphate, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade 1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0551-2023·2023-05-03

    FDA Recalls Glimepiride Tablets for Manufacturing Deviations

    Northwind Pharmaceuticals is voluntarily recalling Glimepiride 2mg tablets distributed nationwide due to Good Manufacturing Practice (CGMP) deviations identified during manufacturing.

    Product
    GLIMEPIRIDE — GLIMEPIRIDE (GLIMEPIRIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0549-2023·2023-05-03

    Drug Recall: Buspirone Tablets Over Manufacturing Process Deviations

    Northwind Pharmaceuticals is recalling Buspirone Hydrochloride 7.5 mg tablets due to manufacturing process deviations. The FDA Class II recall affects bottles distributed nationwide.

    Product
    BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0545-2023·2023-05-03

    FDA recalls Avicel PH-102 microcrystalline cellulose bulk ingredient for specification failure

    DuPont Nutrition is recalling Avicel PH-102 microcrystalline cellulose due to conductivity specification failures in 14 batches distributed across the USA and internationally.

    Product
    Avicel PH-102 NF, Microcrystalline Cellulose NF, Net Content/Gross Weight 20.0 KG / 21.1 KG bulk container, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711, USA; Manufactured in USA; Headquarters: DuPont Nutrition Biosciences ApS, Langebrogade…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V309000·2023-05-02

    Mercedes-Benz Recalls 2022-2023 EQS and EQE Models for Battery Software Defect

    Mercedes-Benz is recalling 3,828 vehicles because high-voltage battery monitoring software may fail to alert drivers of malfunctions, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 450+, redundant EQE 350 4MATIC, AMG EQS 53, EQS 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V305000·2023-04-28

    Ford Explorer backup camera display failure reduces rear visibility

    Certain 2020-2022 Ford Explorer Police Interceptor Utility vehicles have a software issue where the backup camera display does not appear when turned off before reversing, reducing rear visibility and increasing crash risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V307000·2023-04-28

    Winnebago Motorhomes Recalled for Improperly Secured Fuel Hose

    Winnebago is recalling certain 2020-2023 motorhomes due to unsecured fuel hoses that can leak gasoline and increase fire risk. Owners should contact dealers for free inspection and replacement.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, EKKO, SOLIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E036000·2023-04-27

    Chrysler Recalls Mopar Hybrid Battery Packs Due to Fuse Fastener Defect

    Chrysler is recalling Mopar hybrid battery packs because incorrect fasteners may cause excessive heat, leading to power loss and increased crash risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23750·2023-04-27

    Pool Drain Covers Recalled for Entrapment Hazard

    Vijayli-US is recalling about 116 round pool drain covers sold online that do not meet Virginia Graeme Baker Pool and Spa Safety Act standards, posing an entrapment hazard to swimmers and bathers.

    Product
    Pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23191·2023-04-27

    EGL Motor ACE Youth ATVs Fail Safety Standards; Risk of Injury or Death

    EGL Motor is recalling about 4,000 ACE-branded youth all-terrain vehicles (ATVs) that fail federal safety standards. The K125 and C125 models exceed maximum speed limits, and the T125 and C125 models have faulty parking brakes, posing risks of high-speed crashes and collisions.

    Product
    EGL Motor ACE-branded Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23749·2023-04-27

    Ejoyous Pool Drain Covers Recalled for Entrapment Hazard

    Ejoyous pool drain covers sold online do not meet Virginia Graeme Baker Pool and Spa Safety Act standards and pose an entrapment hazard to swimmers and bathers.

    Product
    Ejoyous pool drain covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide