The Recall Desk

State

Oklahoma product recalls

19,713 recalls have nationwide distribution and so reach Oklahoma. 0 additional recalls listed Oklahoma specifically in their distribution scope.

About recalls in Oklahoma

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Oklahoma consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

751–775 of 19713

  • ModerateFDA (Devices)·Z-2117-2026·2026-05-13

    Medline Convenience Kits recalled due to sterilization calibration issues

    Medline Industries is recalling two models of gastrointestinal convenience kits (BAPTIST FLOYD ENDO GI KIT and GI LAB OTHER ENDO KIT) due to calibration issues in sterilization equipment that may have impacted the sterility assurance level of the products.

    Product
    Medline Convenience Kits: 1) BAPTIST FLOYD ENDO GI KIT, Model Number: DYKE1455B; 2) GI LAB OTHER ENDO KIT, Model Number: DYKE1721
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0516-2026·2026-05-13

    Duloxetine Delayed-Release Capsules 20 mg Recalled for Impurity

    Ajanta Pharma USA Inc. is recalling Duloxetine 20 mg delayed-release capsules (Lot PA10734, expiration June 2026) because they contain elevated levels of N-nitroso-Duloxetine impurity above the FDA-recommended limit.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2120-2026·2026-05-13

    Medline Burn Care Kits Recalled Due to Sterilization Calibration Issues

    Medline Industries is recalling three burn care convenience kits because calibration issues with sterilization and packaging equipment could compromise their sterility assurance level.

    Product
    Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PACK-LF, Model Number: DYNJ42829B; 3) BURN CARE PACK-LF, Model Number: DYNJT3437
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2026·2026-05-13

    Duloxetine Delayed-Release Capsules Recalled for Impurity Above FDA Limit

    Ajanta Pharma Ltd. is recalling Duloxetine Delayed-Release Capsules, 60 mg (Lot PA07434, expiration May 2026) because testing found N-nitroso-Duloxetine impurity above the FDA recommended limit of 0.83 ppm.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2126-2026·2026-05-13

    Medline Urology Convenience Kits recalled due to sterilization calibration issues

    Medline Industries is recalling five models of urology convenience kits due to calibration issues in sterilization and packaging equipment that may compromise sterility assurance.

    Product
    Medline Convenience Kits: 1) KIT UROLOGY SLING, Model Number: DYKMBNDL106; 2) KIT UROLOGY SLING, Model Number: DYKMBNDL106A; 3) KIT UROLOGY PENILE REPAIR, Model Number: DYKMBNDL188; 4) KIT UROLOGY PERIPHERAL STIMULA, Model Number: DYKMBNDL189; 5) KIT UROLOGY PERIPHERAL S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2073-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps 23ga Maculorhexis Forceps Recalled

    Katalyst Surgical, LLC is recalling DEX Ophthalmic Tissue Forceps, Model DVF4019-23, due to a field safety corrective action for instructions for use in DEX Forceps and Scissors. The device is distributed worldwide.

    Product
    DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2071-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps instructions for use correction

    Katalyst Surgical is issuing a corrective action for instructions in DEX Ophthalmic Tissue Forceps (Model DVF4014-25-S). The recall affects 80 units distributed worldwide including the US and Peru, Argentina, South Korea, Japan, and France.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2074-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps recalled for instruction updates

    Katalyst Surgical is issuing a Field Safety Corrective Action for 670 units of DEX Ophthalmic Tissue Forceps (Model DVF4019-25) due to updates required in the instructions for use. The device was distributed worldwide.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2079-2026·2026-05-13

    DEX Ophthalmic Tissue Forceps recalled for instructions update

    Katalyst Surgical is issuing a Field Safety Corrective Action for DEX Ophthalmic Tissue Forceps (Model DVF4034-25-S) due to instructions-for-use (IFU) corrections needed.

    Product
    DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2132-2026·2026-05-13

    ZENBONE Resorbable Bone Void Filler Recall Outside Specifications

    Orthorebirth Co Ltd is recalling ZENBONE resorbable bone void filler because the product falls outside standard specifications. The recall affects specific lot numbers distributed nationwide in California and Florida.

    Product
    ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-Z
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2088-2026·2026-05-13

    One Step P in vitro diagnostic test lacks FDA premarket clearance

    The One Step P in vitro diagnostic test (REF 8194) was distributed without required FDA premarket clearance or approval. The manufacturer DFI Co., Ltd. is recalling the device.

    Product
    One Step P in vitro diagnostic test REF: 8194
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0511-2026·2026-05-13

    Buspirone Hydrochloride Tablets 5 mg Recalled for Subpotency

    Unichem Pharmaceuticals USA Inc. is recalling Buspirone Hydrochloride Tablets, USP, 5 mg because the drug is subpotent. The recall affects approximately 10,875 bottles distributed nationwide.

    Product
    BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·25V877000·2026-05-12

    Chrysler Pacifica wheelchair restraints may not lock securely

    Vantage Mobility is recalling 2021–2025 Chrysler Pacifica vehicles equipped with QRT-Deluxe and QRT-Max wheelchair restraints because the retractors may fail to lock, allowing wheelchairs to move unsecured during transit.

    Product
    CHRYSLER — 2021 CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V872000·2026-05-12

    [pending] 2024 TOYOTA HIGHLANDER HYBRID

    Pending LLM rewrite. Source: NHTSA 25V872000.

    Product
    TOYOTA — 2024 TOYOTA HIGHLANDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V876000·2026-05-12

    [pending] 2024 TOYOTA SIENNA HYBRID

    Pending LLM rewrite. Source: NHTSA 25V876000.

    Product
    TOYOTA — 2024 TOYOTA SIENNA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V874000·2026-05-12

    [pending] 2024 KIA SPORTAGE

    Pending LLM rewrite. Source: NHTSA 25V874000.

    Product
    KIA — 2024 KIA SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V791000·2026-05-11

    [pending] 2022 THOR MOTOR COACH SEQUENCE

    Pending LLM rewrite. Source: NHTSA 25V791000.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH SEQUENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V794000·2026-05-11

    [pending] 2021 KIA K5

    Pending LLM rewrite. Source: NHTSA 25V794000.

    Product
    KIA — 2021 KIA K5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V792000·2026-05-11

    [pending] 2022 THOR MOTOR COACH TELLARO

    Pending LLM rewrite. Source: NHTSA 25V792000.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH TELLARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V793000·2026-05-11

    [pending] 2021 FORD E-350

    Pending LLM rewrite. Source: NHTSA 25V793000.

    Product
    FORD — 2021 FORD E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V711000·2026-05-10

    [pending] 2025 MERCEDES-BENZ AMG G63

    Pending LLM rewrite. Source: NHTSA 25V711000.

    Product
    MERCEDES-BENZ — 2025 MERCEDES-BENZ AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V712000·2026-05-10

    [pending] 2025 MERCEDES-BENZ SPRINTER 2500

    Pending LLM rewrite. Source: NHTSA 25V712000.

    Product
    MERCEDES-BENZ — 2025 MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V709000·2026-05-10

    Thor Motor Coach recreational vehicles with unsecured LP generator hose

    Thor Motor Coach is recalling certain 2025–2026 recreational vehicles because a P-clamp may not have been installed to secure the Liquid Propane (LP) generator hose, which could contact the exhaust and increase fire risk.

    Product
    THOR MOTOR COACH — 2025 THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V710000·2026-05-10

    [pending] 2023 JEEP WRANGLER 4XE

    Pending LLM rewrite. Source: NHTSA 25V710000.

    Product
    JEEP — 2023 JEEP WRANGLER 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V707000·2026-05-10

    [pending] 2025 FOREST RIVER STEALTH EVO

    Pending LLM rewrite. Source: NHTSA 25V707000.

    Product
    FOREST RIVER — 2025 FOREST RIVER STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide