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.

58076–58100 of 79657

  • CriticalFDA (Food)·F-2580-2015·2015-07-01

    Blue Bell Rum Raisin Ice Cream Recalled Due to Listeria Infections

    Blue Bell Creameries is recalling Rum Raisin Still a ice cream after five patients in Kansas were infected with Listeria monocytogenes.

    Product
    Blue Bell Ice Cream Rum Raisin Still a 1/2 Gal (2 QTS)
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Food)·F-2498-2015·2015-07-01

    Blue Bell Ice Cream Recalled Due to Listeria Infections

    Blue Bell Creameries is recalling Red, White, & Blue Bell ice cream after five patients in Kansas were infected with Listeria monocytogenes.

    Product
    Blue Bell Red, White, & Blue Bell One Pint (473 mL)
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Devices)·Z-1820-2015·2015-07-01

    Hill-Rom Steriseal-Cannula Ophthalmic Recall Due to Dislodgement Risk

    Hill-Rom is recalling Steriseal-Cannula Ophthalmic handpieces because the metal cannula can rotate and become dislodged from the plastic handpiece.

    Product
    Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2769-2015·2015-07-01

    Crystal Fresh Recalls Cheesecake Shave Ice for Undeclared Milk Allergen

    Crystal Fresh is recalling SNOBIZ Cheesecake Shave Ice Flavor due to an undeclared milk allergen. The product was distributed in multiple US states and Canada.

    Product
    SNOBIZ CHEESECAKE SHAVE ICE FLAVOR, 10 pouches/carton; 8 cartons/case (80 pouches total per case), 104 gram per pouch, metallized pouch.
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-2737-3015·2015-07-01

    Natural Grocers Raw Macadamia Nuts Recalled for Salmonella Contamination Risk

    Vitamin Cottage Natural Food Markets is recalling specific lots of Natural Grocers Raw Macadamia Nuts due to potential Salmonella contamination.

    Product
    Natural Grocers Raw Macadamia Nuts, Net Wt. 10 oz. package, Sealed plastic bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2773-2015·2015-07-01

    Mi Costenita Bocadin Wafers Recalled for Undeclared Milk Allergen

    Yoli, Inc. is recalling Mi Costenita Bocadin chocolate-covered wafers due to undeclared milk allergens. The product was distributed nationwide in 26 states.

    Product
    Chocolate covered wafers (Bocadin) in plastic packaging sold under the Mi Costenita brand and packaged and distributed by Yoli, Inc.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V420000·2015-07-01

    Gillig Recalls 2010-2015 Low Floor Buses Due to Fire Risk

    Gillig is recalling 2010-2015 Low Floor transit buses because a power cable may chafe a fuel line, increasing fire risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1835-2015·2015-07-01

    Stryker Recalls Optical Access Systems Due to Fracture Risk

    Stryker is recalling specific Optical Access Systems because they may fracture at the tip, leaving fragments at the surgical site.

    Product
    Optical Access System; 5mm x 100mm and 12mm x 100mm; Model #: CTR03 and CTR73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1834-2015·2015-07-01

    Stryker Recalls Fios First Entry Trocars Due to Fracture Risk

    Stryker is recalling Fios First Entry trocars because some may fracture at the distal tip, leaving fragments at the surgical site.

    Product
    Fios First Entry; 5mm x 100mm and 12mm x 100mm; Model #:CTF03 and CTF73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V418000·2015-07-01

    Nissan Recalls Juke, Cube, Versa for Sticking Start/Stop Button

    Nissan is recalling 2013-2014 Juke, Cube, and 2014 Versa vehicles because the engine start/stop button may stick, potentially causing the engine to shut off while driving.

    Product
    NISSAN — NISSAN VERSA, JUKE, CUBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1831-2015·2015-07-01

    Stryker Recalls SERFAS 90 Degree Energy Probes Due to Fragmentation

    Stryker Endoscopy is recalling 22,063 SERFAS 90 degree Energy Probes because fragments of the probe have been reported to break off into patients during arthroscopic procedures.

    Product
    SERFAS 90 degree Energy Probe, Part Number 279-350-101; SERFAS Energy Probes are indicated for arthroscopic procedures of the knee, shoulder, ankle, hip, elbow and wrist. Specifically, the probes are used for resection, ablation and coagulation of soft tissue, as well as the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1809-2015·2015-07-01

    Teleflex Recalls Lifesaver Manual Resuscitators Due to Potential Intake Port Blockage

    Teleflex Medical is recalling 9,333 units of Lifesaver Single Patient Use Manual Resuscitators because the intake port may be blocked, causing the bag to fail to fill.

    Product
    Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual resuscitator with pressure monitoring port is a disposable medical device intended for use on patients requiring temporary augmentation of ventilation with or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1836-2015·2015-07-01

    Stryker Recalls Trocars Due to Reported Fracture at Distal Tip

    Stryker is recalling specific cannula and seal models because they may fracture at the tip, leaving fragments at the surgical site.

    Product
    Cannula and Seal; 5mm x 100mm and 12mm x 100mm Model #: CTS02 and CTS22. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1827-2015·2015-07-01

    Fresenius NaturaLyte Liquid Bicarbonate Concentrate Recalled for Bacterial Contamination

    Fresenius Medical Care is recalling NaturaLyte Liquid Bicarbonate Concentrate due to bacterial contamination. The product is used in hemodialysis machines.

    Product
    NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for Hemodialysis (liquid), 6.4 Liter Bottle Catalog Number: 08-4000-LB This concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15739·2015-07-01

    Otteroo Recalls Inflatable Baby Floats Due to Drowning Risk

    Otteroo is recalling about 3,000 inflatable baby floats because seams can leak air and deflate, posing a drowning risk. No injuries have been reported.

    Product
    Otteroo Inflatable Baby Floats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1841-2015·2015-07-01

    Remel VersaTREK Instrument Series 240 Recalled for False Positive Reports

    Remel Inc. is recalling 143 VersaTREK Instrument Series 240 devices because their use may result in false positive reports. The devices are used to cultivate microorganisms from blood and other sterile bodily fluids.

    Product
    VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and recovering microorganisms, especially bacteria and yeasts, from blood and other normally sterile bodily fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2753-2015·2015-07-01

    Lavoi Epi Bread Recalled for Undeclared Peanut and Tree Nut Allergens

    Lavoi Corporation is recalling specific Epi bread products because they were made with wheat gluten containing undeclared peanut and tree nut residue.

    Product
    Epi breads, 8" Extra Wide Sliced Hoagie, 7" Hoagie Butterfly Sliced, 54 count per case and 9.5" Crusty Hoagie, 45 count per case, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.
    Category
    Food
    Distribution
    27 states
  • HighNHTSA·15V419000·2015-07-01

    Subaru Recalls 2012 Impreza Vehicles Due to Passenger Air Bag Defect

    Subaru is recalling 2012 Impreza vehicles because the Occupant Detection System may deactivate, preventing the front passenger air bag from deploying in a crash.

    Product
    SUBARU — SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2757-2015·2015-07-01

    Fire House Subs Bread Recalled for Undeclared Peanut and Tree Nut Allergens

    Lavoi Corporation is recalling Fire House Subs bread rolls due to undeclared peanut and/or tree nut residue in the wheat gluten used.

    Product
    Fire House Subs, Medium White Sub Roll, and Large White Sub Roll, 48 and 45 count case, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-1819-2015·2015-07-01

    Orthofix Centurion POCT System Drill Guide Recall for Depth Setting Risk

    Orthofix is recalling 36 Centurion POCT System Drill Guides because the thumb button may remain unlocked, allowing the drill stop to rotate unintentionally and change the depth setting.

    Product
    ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN 69-1012. Drill Guides are used to interface with various drill tips during the drilling procedure of bone preparation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1837-2015·2015-07-01

    DeRoyal Recalls Custom Surgical Kits with Defective Medtronic Gloves

    DeRoyal Industries is recalling custom surgical kits containing Medtronic Devon Light Gloves due to splits or holes.

    Product
    Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves: ANGIO TRAY, REF 50-12127; NEURO SPINE TRAY, LAP CHOLE TRACECART(R), REF 53-1931; MINOR PROCEDURE TRACECART (R), REF 53-1932; MAJOR PROCEDURE TRACECART (R), 53-1933; Cover Light Handle Flexible, REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2762-2015·2015-07-01

    Walmart Brand Bread Recalled for Undeclared Peanut and Tree Nut Allergens

    Lavoi Corporation is recalling Walmart brand bread because it was made with wheat gluten containing undeclared peanut and/or tree nut residue.

    Product
    Walmart brand bread, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236
    Category
    Food
    Distribution
    27 states
  • HighFDA (Food)·F-2749-2015·2015-07-01

    Epi White Hoagie Sliced Bread Recalled for Undeclared Peanut and Tree Nut

    Lavoi Corporation is recalling Epi White Hoagie Sliced Bread because it was made with wheat gluten containing undeclared peanut and/or tree nut residue.

    Product
    Epi breads, 12" White Hoagie Sliced, 45 count per case, Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas, TX 75236.
    Category
    Food
    Distribution
    27 states