The Recall Desk

State

Oklahoma product recalls

73,741 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,040
Severe
1,493
Most recent
2026-10-28

Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38126–38150 of 79563

  • ModerateFDA (Drugs)·D-0482-2019·2019-02-20

    US Compounding Recalls LET Gel 4% Syringes Due to Missing Lot and Expiration Dates

    US Compounding Inc is recalling 1,931 syringes of LET Gel 4% because the labels are missing specific lot and expiration dates.

    Product
    LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0490-2019·2019-02-20

    Valeant Recalls Cardizem CD Capsules for Dissolution Failures

    Valeant Pharmaceuticals is recalling 22 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.

    Product
    CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0828-2019·2019-02-20

    Ottobock MagValve Recall for Prosthetic Socket Air Evacuation Defect

    Ottobock is recalling 110 MagValve units used in prosthetic sockets because some valve inserts have a smaller diameter than specified.

    Product
    21Y15 MagValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0488-2019·2019-02-20

    Valeant Recalls Cardizem CD Capsules for Dissolution Failures

    Valeant Pharmaceuticals is recalling 206 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, meaning the drug may not release properly.

    Product
    CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0827-2019·2019-02-20

    Ottobock PushValve Upper Part Recalled for Diameter Specification Defect

    Ottobock is recalling PushValve upper parts because some installed valve inserts have a diameter smaller than the specification.

    Product
    21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0487-2019·2019-02-20

    Valeant Recalls Cardizem CD Capsules for Dissolution Failures

    Valeant Pharmaceuticals is recalling 1,023 bottles of Cardizem CD (diltiazem hydrochloride) 120 mg capsules because they failed to meet dissolution specifications.

    Product
    CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0491-2019·2019-02-20

    Valeant Recalls Diltiazem HCl Capsules for Dissolution Failures

    Valeant Pharmaceuticals is recalling 23,884 bottles of Diltiazem HCl CD capsules because they failed dissolution specifications, potentially affecting drug release.

    Product
    Diltiazem HCl CD capsules, 360 mg, 90-count bottles, Rx Only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0483-2019·2019-02-20

    Akorn Recalls COSOPT Ophthalmic Solution Due to Stability Failures

    Akorn Inc. is recalling 30,794 bottles of COSOPT Ophthalmic Solution because the product failed stability specifications for opalescence.

    Product
    COSOPT Ophthalmic Solution, USP, (2% Dorzolamide Hydrochloride, 0.5% Timolol Maleate), 10 mL dropper bottle, Sterile, Rx only, Distributed by: Akorn, Inc., Lake Forest, IL, NDC: 17478-605-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0822-2019·2019-02-20

    Luminex Recalls Verigene BC-GP Utility Kits Due to Labeling Error

    Luminex Corporation is recalling Verigene BC-GP Utility Kits because they were incorrectly labeled with Amplification Tray labels.

    Product
    Vergene Amplification Tray - 700uL, BC-GP REF 20-011-018 The Verigene(R) Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the sample-to-result Verigene System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V108000·2019-02-19

    Keystone Recalls 2019 Crossroads Redwood Trailers Due to Pin Box Bolt Issue

    Keystone is recalling 2019 Crossroads Redwood recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.

    Product
    CROSSROADS — CROSSROADS REDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19067·2019-02-19

    Academy Sports + Outdoors Recalls Outdoor Gourmet Turkey Keg Fryers

    Academy Sports + Outdoors is recalling Outdoor Gourmet Turkey Keg turkey fryers because the spout can leak oil, posing a fire hazard.

    Product
    Outdoor Gourmet Turkey Keg turkey fryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V109000·2019-02-19

    Kia Recalls 2015-2018 Sedona Vehicles Due to Wiring Harness Defect

    Kia is recalling 2015-2018 Sedona vehicles with manual front passenger seats because a wiring harness may break, potentially allowing the airbag to deploy and injure a child.

    Product
    KIA — KIA SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V102000·2019-02-15

    Goshen Shuttle Buses Recalled for Wheelchair Lift Cam Failure

    Eldorado is recalling 2012-2018 Goshen shuttle buses because a wheelchair lift cam may fail, allowing the platform to rise too high and risk injury.

    Product
    GOSHEN — GOSHEN GCII, IMPULSE, PACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V099000·2019-02-15

    Ford Recalls 2019 Fusion Energi for High Voltage Protection Defect

    Ford is recalling 2019 Fusion Energi Hybrid vehicles because they may not adequately protect against high voltage contact during normal operation.

    Product
    FORD — FORD FUSION ENERGI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V100000·2019-02-15

    New Flyer Transit Buses Recalled for Shattering Roof Hatch Glass

    New Flyer is recalling 172 transit buses because the rooftop emergency escape hatch glass may shatter in extreme cold, posing an injury risk to passengers.

    Product
    NEW FLYER — NEW FLYER XN40, XDE60, XD40, XE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V097000·2019-02-14

    Toyota Recalls 2019 Camry and Avalon Hybrids for Fuel Leak Risk

    Toyota is recalling 2019 Camry Hybrid and Avalon Hybrid vehicles because the fuel filler pipe may not be properly connected, posing a fire risk.

    Product
    TOYOTA — TOYOTA CAMRY HYBRID, AVALON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V090000·2019-02-14

    Ferrari Recalls 2,150 Vehicles for Fuel Leak Fire Risk

    Ferrari is recalling 2,150 vehicles because a cracked fuel vapor separator may leak fuel, increasing the risk of fire.

    Product
    FERRARI — FERRARI 488 SPIDER, GTC4LUSSO, LAFERRARI, 488 GTB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19064·2019-02-14

    PurpleAir Recalls Power Supply Units for Air Sensors Due to Fire and Burn Hazards

    PurpleAir is recalling PowerStream power supply units for air sensors because they can overheat, posing fire and burn hazards. No injuries have been reported, but 27 reports of sparks or smoke were received.

    Product
    PowerStream Power Supply Units for Air Sensors
    Category
    Consumer Product
    Distribution
    Distributed nationwide