The Recall Desk

State

Oklahoma product recalls

73,833 recalls have nationwide distribution and so reach Oklahoma. 5,824 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,824
Critical
1,040
Severe
1,494
Most recent
2026-11-14

Of the 5,824 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 1,494 (26%) are Severe.

These figures cover only the 5,824 recalls whose distribution notice names Oklahoma specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58126–58150 of 79657

  • HighFDA (Food)·F-2759-2015·2015-07-01

    Zaxbys Nibbler Buns Recalled for Undeclared Peanut and Tree Nut Allergens

    Lavoi Corporation is recalling Zaxbys Nibbler Buns because they were made with wheat gluten containing undeclared peanut and/or tree nut residue.

    Product
    Zaxbys, Nibbler Bun, 180 count case, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-1833-2015·2015-07-01

    ArthroCare Medical Recalls PROcise XP Wand Due to Component Failure

    ArthroCare Medical is recalling 2,355 PROcise XP Wand units because a potential component failure may cause the device to become inoperable during use.

    Product
    PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1844-2015·2015-07-01

    Volcano PV .035 Catheter Recalled for Incorrect Shelf Life Labeling

    Volcano Corporation is recalling 162 PV .035 Catheters because they were labeled with incorrect shelf life dates during a relabeling procedure.

    Product
    Volcano PV .035 Catheter: Part number: 88901; Product Usage: The Volcano PV .035 is indicated for use in the evaluation of vascular morphology in blood vessels of the peripheral vasculature by providing a cross-sectional image of such vessels. The device is an adjunct to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1832-2015·2015-07-01

    ArthroCare EVAC 70 XTRA Plasma Wand Recall for Component Failure

    ArthroCare Medical Corporation is recalling EVAC 70 XTRA plasma wands due to potential component failure that may cause the device to become inoperable.

    Product
    EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck, oral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1845-2015·2015-07-01

    Volcano Prestige Plus J-Tip Wire Recalled for Incorrect Shelf Life Labeling

    Volcano Corporation is recalling 162 Prestige Plus 185cm J-Tip pressure wires because they were labeled with incorrect shelf life dates during a relabeling procedure.

    Product
    Prestige Plus 185cm J-Tip: Part number: 9185J; Product Usage: The Prestige Plus Wire is indicated for use to measure pressure in blood vessels including both coronary and peripheral vessels, during diagnostic angiography and/or any interventional procedures. Blood pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1824-2015·2015-07-01

    CooperSurgical Recalls Vaginal Speculums Due to Incorrect Packaging

    CooperSurgical is recalling 9,400 McKesson Medi-Pak Vaginal Speculums because small-sized speculums were incorrectly packaged in bags labeled for medium-sized speculums.

    Product
    McKesson Medi-Pak Vaginal Speculum, 10/bag Reorder No. 11-8309 Used to expose interior of the vagina to facilitate visualization during gynecological and obstetrical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1830-2015·2015-07-01

    Cook Inc. Recalls LapSac Surgical Tissue Pouches Due to Labeling Error

    Cook Inc. is recalling 123,184 LapSac Surgical Tissue Pouches because the labeling includes information not stated in the intended use.

    Product
    LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue during, or prior to, surgical removal and/or morcellation. The device is a reinforced pouch with an inner liner and drawstring closure. The device may be used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1149-2015·2015-07-01

    Indiana Botanic Gardens Recalls Dr Blue Pain Relieving Gel Due to Blending Issues

    Indiana Botanic Gardens is recalling Dr Blue Pain Relieving Gel because the product may not be uniformly blended, resulting in non-uniform distribution of the active ingredient menthol.

    Product
    Dr Blue Pain Relieving Gel, (4.6% menthol), For temporary relief of minor aches and pains of muscles and joints, a) 2 oz. Tube, NDC 10578-035-05, b) 5 oz. Jar, NDC 10578-035-04, Manufactured by Indiana Botanic Gardens, Hobart, IN 46342
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1148-2015·2015-07-01

    Actavis Recalls Lutera Birth Control Due to Outdated Package Inserts

    Actavis Inc is recalling Lutera birth control tablets because the packs were distributed with out-dated package inserts.

    Product
    Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP), 28 day Regimen, 6 Tablet Dispensers per box, 28 Tablets Each, Rx Only, Manufactured for: Watson Pharm, Inc., a subsidiary of Watson Pharmaceutical, Inc., Corona, CA 92880, Manufactured by: Patheon, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1839-2015·2015-07-01

    Ethicon Recalls Surgical Sutures Due to Incomplete Labeling

    Ethicon is recalling specific lots of Fast Absorbing Plain Gut sutures because the box and foil labels are incomplete.

    Product
    Ethicon Fast Absorbing Plain Gut - MultiPass Needles, Sterile, Absorbable Surgical Suture, 5-0 (1.5 metric), 18" (45 cm), Conventional Cutting, Lot #JD6163, Exp: July 2019. Fast absorbing surgical gut suture is a strand of collagenous material prepared from the submucosal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1147-2015·2015-07-01

    Bracco Recalls E-Z-CAT Dry Barium Sulfate Due to Viscosity Failures

    Bracco Diagnostic Inc. is recalling E-Z-CAT Dry Barium Sulfate for Suspension because the product failed stability specifications for viscosity.

    Product
    E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing), 23 g foil pouches, Rx only, Manufactured by E-Z-EM Canada Inc. a subsidiary of E-Z-EM Inc., Lake Success NY NDC 32909-727-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V412000·2015-06-30

    Oshkosh Recalls 2015 S-Series Trucks Due to Torque Converter Paint Issue

    Oshkosh is recalling 24 model year 2015 S-Series concrete mixer glider trucks because paint on the torque converter may soften, causing bolts to loosen and potentially leading to a loss of drive power.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15737·2015-06-30

    Yamaha Recalls SRViper Snowmobiles Due to Brake Failure Risk

    Yamaha is recalling about 200 SRViper snowmobiles because the brake line can contact the clutch, causing brake failure and posing a risk of injury or death.

    Product
    Yamaha SRViper snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V413000·2015-06-30

    Goshen Buses Recalled for Fraying Passenger Seat Belts

    Goshen Coach is recalling 2013-2015 buses because passenger seat belts may rub against metal frames and fray, potentially failing to restrain occupants in a crash.

    Product
    GOSHEN — GOSHEN IMPULSE, G-FORCE ACCESS, G-FORCE, G-FORCE LTD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V416000·2015-06-30

    GM Recalls 2014-2015 Chevrolet Sonic and Spark for Radio Software Defect

    General Motors is recalling 2014-2015 Chevrolet Sonic and Spark vehicles because a radio software issue may disable safety warning chimes, increasing the risk of theft and injury.

    Product
    CHEVROLET — CHEVROLET SONIC, SPARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V415000·2015-06-30

    GM Recalls SUVs for Power Liftgate Gas Strut Wear Risk

    General Motors is recalling 2007-2012 Buick Enclave, Chevrolet Traverse, GMC Acadia, and Saturn Outlook vehicles because power liftgate gas struts may wear prematurely, causing the liftgate to fall suddenly.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE, OUTLOOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15173·2015-06-30

    Technosport Recalls Omersub Scuba Mask Due to Shattering Lens Hazard

    Technosport is recalling Omersub Zero Cube scuba masks because non-conforming glass lenses can shatter during normal use, posing an injury hazard.

    Product
    Omersub Zero Cube scuba diving mask
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V410000·2015-06-29

    Yamaha Recalls WR250X and WR250R Motorcycles Due to Stator Coil Defect

    Yamaha is recalling 2008-2015 WR250X and WR250R motorcycles because a stator coil defect may cause the battery to die and the engine to stall, increasing crash risk.

    Product
    YAMAHA — YAMAHA WR250X, WR250R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·095-2015·2015-06-26

    OFT Inc Recalls Beef Extracts Produced Without Import Inspection

    OFT Inc is recalling approximately 67,232 pounds of beef leg bone extract and beef concentrate products produced in Australia and New Zealand that were not presented for U.S. import inspection.

    Product
    OFT Inc Recalls Beef Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide