The Recall Desk

State

Oklahoma product recalls

72,936 recalls have nationwide distribution and so reach Oklahoma. 5,788 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,788
Critical
1,033
Severe
1,238
Most recent
2026-09-09

Of the 5,788 recalls naming Oklahoma we have scored against our rubric, 1,033 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,238 (21%) are Severe.

These figures cover only the 5,788 recalls whose distribution notice names Oklahoma specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3076–3100 of 78724

  • HighFDA (Devices)·Z-1433-2026·2026-03-04

    Medline trunk kits recalled over saline wound wash sterility failure

    Medline is recalling five Trunk Kit convenience kits because the manufacturer of the sterile saline wound wash they contain may not have met the required sterility assurance level.

    Product
    Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM2013; 3) TRUNK KIT 1EA, Model Number: DYKM2013A; 4) RN TRUNK KIT, Model Number: DYKM2699; 5) TRUNK KIT, Model Number: DYKTRUNK1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0352-2026·2026-03-04

    BioGlo fluorescein ophthalmic strips recalled over sterility assurance failure

    Wizcure Pharmaa is recalling all lots of BioGlo Fluorescein Sodium Ophthalmic Strips in 100-strip packs because the products were not manufactured in conformance with current good manufacturing practices.

    Product
    BioGlo Fluorescein Sodium Ophthalmic Strips USP, 100 diagnostic strips, Manufactured by Omni Lens PVT. Ltd., 5 - Samrudhhi, Opp. Sakar-III, Navrangpura, Ahmedabad, Gujarat, India - 380014, Email:[email protected], Manufactured for & disibruted by: HUB Pharmaceuticals, LLC, 8767 E
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1463-2026·2026-03-04

    Medline Kits with Tego Connectors Recalled Due to Silicone Seal Defects

    Medline Industries, LP is recalling specific Medline Kits containing Tego Connectors because the silicone seals may dome or tear, potentially causing fluid leakage or blocked paths.

    Product
    Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1439-2026·2026-03-04

    Olympus resection inner sheath A22040A recalled over ceramic tip breakage

    Olympus is recalling its Resection Inner Sheath for 26 Fr outer sheath, model A22040A, used in urologic applications, after complaints that the ceramic tip can break.

    Product
    Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0348-2026·2026-03-04

    Vista Meibo Tears eye drops recalled over sterility assurance failure

    Wizcure Pharmaa is recalling all lots of Vista Meibo Tears Propylene Glycol 0.6% eye drops because the products were not manufactured in conformance with current good manufacturing practices.

    Product
    VISTA MEIBO TEARS PROPYLENE GLYCOL 0.6% W/V ADVANCED DRY EYE RELIEF LUBRICATING DROPS 10 ML — VISTA MEIBO TEARS PROPYLENE GLYCOL 0.6% W/V ADVANCED DRY EYE RELIEF LUBRICATING DROPS 10 ML (PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0351-2026·2026-03-04

    Bio Glo fluorescein strips 300-count recalled over sterility assurance failure

    Wizcure Pharmaa is recalling all lots of Bio Glo Fluorescein Sodium Ophthalmic Strips in 300-strip packs because the products were not manufactured in conformance with current good manufacturing practices.

    Product
    Bio Glo Fluorescein Sodium Ophthalmic Strips USP, 300 diagnostic strips, Manufactured Omni Lens Pvt Ltd 5 - Samruddhi, Opp. Sakar - III, Navrangpura, Ahmedabad - 380014, India, Email:[email protected], Manufactured for & distributed by: HUB Pharmaceuticals, LLC, 8767 E Via de Ven
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1440-2026·2026-03-04

    Olympus resection inner sheath recalled after ceramic tip breakage complaints

    Olympus is recalling its Resection Inner Sheath for 26 Fr outer sheath, model A22040T, used in urologic applications, after complaints that the ceramic tip of the resection sheath can break.

    Product
    Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1447-2026·2026-03-04

    Olympus inner sheath model A2660 recalled over ceramic tip breakage

    Olympus is recalling its Inner Sheath, model A2660, used for endoscopic diagnosis and treatment in urological applications, after complaints that the ceramic tip of the resection sheath can break.

    Product
    Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1473-2026·2026-03-04

    Medtronic tissue stabilizer recalled after tubing was assembled in reverse

    Medtronic is recalling one lot of the Octopus Nuvo Tissue Stabilizer after identifying an assembly issue in which the short and long tubes were attached to the wrong ends of the canister.

    Product
    Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1462-2026·2026-03-04

    Edermy PIE PAK units recalled for lacking FDA 510(k) clearance

    Edermy LLC is recalling PIE PAK models P2HC-A, P2HC-S and P2HC because the devices lack 510(k) clearance from the FDA.

    Product
    PIE PAK Models: P2HC-A, P2HC-S, P2HC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1472-2026·2026-03-04

    Adapt Pump Medical Device Recalled Due to Microclimate Management Function Failure

    Agiliti Health - Ellis is recalling Adapt Pumps (Model 61600200) because the Microclimate Management function may fail to re-engage after using the Autofirm function.

    Product
    Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware version 1.3.0; Mattress, Air Flotation, Alternating Pressure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0343-2026·2026-03-04

    Eptifibatide Injection Labeling Error Recall by Slate Run

    Slate Run Pharmaceuticals is recalling Eptifibatide Injection due to a labeling error on the carton, which incorrectly describes the dosing instructions.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2026-EXP·2026-03-03

    Ajinomoto Recalls Chicken and Pork Fried Rice Due to Glass Contamination

    Ajinomoto Foods North America is expanding a recall for frozen fried rice, ramen, and shu mai products due to possible glass contamination. No injuries have been reported.

    Product
    Ajinomoto Foods North America — Ajinomoto Foods North America, Inc. Expands Recall for Chicken and Pork Fried Rice, Ramen, and Shu Mai Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·26V117000·2026-03-03

    Ford and Lincoln vehicles recalled due to windshield wiper motor failure risk

    Ford Motor Company is recalling certain 2020-2022 Ford and Lincoln vehicles because the windshield wiper motors may fail, potentially reducing visibility and increasing crash risks.

    Product
    FORD — FORD, LINCOLN ESCAPE, EXPLORER, AVIATOR, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V124000·2026-03-03

    Ford Bronco and Edge Vehicles Recalled for Camera Software Issue

    Ford is recalling certain 2021-2026 Bronco and 2021-2024 Edge vehicles because the rearview camera may fail to display an image due to an overheating module.

    Product
    FORD — FORD BRONCO, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V123000·2026-03-03

    Lincoln Corsair and Ford vehicles recalled for rearview camera display issues

    Ford Motor Company is recalling certain 2020-2024 Lincoln and Ford vehicles because the center display may show an inverted rearview image, increasing crash risks.

    Product
    FORD — FORD, LINCOLN ESCAPE, EXPLORER, AVIATOR, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V120000·2026-03-03

    Ford Recalls 2026 Lincoln Navigator for Driver Seat Software Defect

    Ford is recalling 2026 Lincoln Navigator vehicles because the driver seat software may malfunction at low speeds, causing the seat to move unexpectedly and increasing crash risk.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V122000·2026-03-03

    2025 Ford Vehicles Recalled for EGR Valve Failure Risk

    Ford is recalling certain 2025 vehicles due to a potential EGR valve failure that could cause an unexpected loss of drive power, increasing crash risk.

    Product
    FORD — FORD, LINCOLN BRONCO, BRONCO SPORT, ESCAPE, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03012026-01·2026-03-01

    USDA Issues Public Health Alert for Punahele Beef Jerky Due to Undeclared Soy

    USDA FSIS issued a public health alert for Punahele beef jerky products containing undeclared soy lecithin. Consumers are advised not to consume the items.

    Product
    Punahele Jerky Company, Inc. — FSIS Issues Public Health Alert for Ready-To-Eat Beef Jerky Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·26288·2026-02-26

    Trankerloop Baby Bath Seats Recalled Due to Drowning Risk

    Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.

    Product
    Trankerloop Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide