The Recall Desk

State

Oklahoma product recalls

73,809 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total
5,823
Critical
1,040
Severe
1,494
Most recent
2026-11-04

Of the 5,823 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.

Which agencies issued them

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44001–44025 of 79632

  • HighFDA (Food)·F-0337-2018·2017-11-29

    Astor Chocolate Recalls Dark Chocolate Covered Cranberries for Undeclared Milk

    Astor Chocolate Corporation is recalling Dark Chocolate Covered Cranberries due to an undeclared milk allergen. The product was distributed across multiple US states and Canada.

    Product
    Astor Chocolate Corporation Brand Dark Chocolate Covered Cranberries in Astor or Customer Logo packaging a. 1 oz. giveaway type package sizing b. 4 oz. giveaway type package sizing c. No best by date on units d. Individual cases sold to Astor branded customers i. Case…
    Category
    Food
    Distribution
    22 states
  • HighCPSC·18046·2017-11-29

    Libbey Recalls Bourbon Taster Glasses Due to Laceration Hazard

    Libbey Glass is recalling approximately 229,000 Bourbon Taster Glasses because they can break during normal use, posing a laceration hazard.

    Product
    Bourbon Taster Glasses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0128-2018·2017-11-29

    Exactech Recalls Optetrak Offset Tibial Trays Due to Design Incompatibility

    Exactech, Inc. is recalling 114 Optetrak Offset Tibial Trays and Screws due to a design incompatibility with certain offset spine stiffener screws and constrained condylar tibial inserts.

    Product
    Optetrak Offset Tibial Tray and Screws, Size 1DeltaF/0T, Beta, Ref 208-04-12, Sterile, RX.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0163-2018·2017-11-29

    Medline Plastic Transfer Belts Recalled for Locking Mechanism Failure

    Medline Industries is recalling 1,428 plastic transfer belts because the locking mechanism may fail, allowing the strap to slip through the buckle.

    Product
    Transfer/Gait Belt, Plastic, Wipeable, packaged in plastic bag, 36 plastic bags per box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0161-2018·2017-11-29

    Zimmer Biomet Recalls ROSA Surgical Device Software

    Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue affecting cooperative endoscopy mode.

    Product
    ROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2018·2017-11-29

    Lorazepam Tablets Recalled Due to Incorrect Strength Labeling

    Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0093-2018·2017-11-29

    West-Ward Recalls Dexamethasone Sodium Phosphate Injection Due to Impurities

    West-Ward Pharmaceuticals is recalling specific lots of Dexamethasone Sodium Phosphate Injection because of high out-of-specification results for a related compound.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0094-2018·2017-11-29

    West-Ward Recalls Dexamethasone Sodium Phosphate Injection Due to Impurity

    West-Ward Pharmaceuticals is recalling Dexamethasone Sodium Phosphate Injection due to high levels of a related compound impurity.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V761000·2017-11-27

    Daimler Recalls 2008-2018 Trucks for Brake Light Switch Defect

    Daimler Trucks North America is recalling 2008-2018 Freightliner and Western Star trucks because the brake light switch may fail to activate lights after hard braking, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 4700, 5700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0395-2018·2017-11-22

    doTERRA Recalls Slim & Sassy TrimShake for Undeclared Milk Allergen

    doTERRA is voluntarily recalling Slim & Sassy TrimShake mixes because they contain an undeclared milk allergen.

    Product
    Slim & Sassy¿ TrimShake Vanilla, SKU 35180001, 1 lb 5.9 oz, HDPE tub
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0394-2018·2017-11-22

    doTERRA Recalls Slim & Sassy TrimShake for Undeclared Milk Allergen

    doTERRA is voluntarily recalling Slim & Sassy TrimShake chocolate and vanilla mixes because they contain an undeclared milk allergen.

    Product
    Slim & Sassy¿ TrimShake Chocolate, SKU 35200001, 1 lb 5.9 oz, HDPE tub
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V753000·2017-11-22

    DRV Recalls RVs with Defective Kidde Fire Extinguishers

    DRV Suites is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog, require excessive force to activate, or have nozzles that detach.

    Product
    DRV — DRV MOBILE SUITE, MOBILE SUITE ESTATES, SELECT, TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2018·2017-11-22

    WalkMed Infusion Pump Reservoir Bags Recalled for Fluid Leaks

    WalkMed, LLC is recalling 25,920 infusion pump reservoir bags due to reported fluid leaks at the luer connection.

    Product
    Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed Infusion Pump Part Number 204821 Catalog Number IPR-150/10 150 mL The WalkMed Reservoir Bag is designed for use with the WalkMed 350VL Ambulatory pump and is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0339-2018·2017-11-22

    Aurora Dark Chocolate Cherries Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Cherries in 8.5 oz cups and 11 oz tubs due to undeclared milk.

    Product
    Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz. Plastic Cup 11 oz. Square Plastic Tub
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V754000·2017-11-22

    Bison Recalls 2010 Recreational Trailers Due to Fire Extinguisher Defect

    Bison Coach is recalling 2010 Stratus, Aluma Sport, Trail Express, and Trail Hand trailers because their fire extinguishers may clog or detach, posing injury risks.

    Product
    BISON — BISON STRATUS, TRAIL HAND, ALUMA SPORT, TRAIL EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0096-2018·2017-11-22

    Zimmer Biomet ROSA Surgical Device Recalled for Potential Force Sensor Break

    Zimmer Biomet is recalling 21 ROSA Surgical Devices due to a possible break in the Force Sensor connector. The devices were distributed to facilities in Ohio, Michigan, and Texas.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0099-2018·2017-11-22

    Zimmer Biomet Recalls ROSA Surgical Devices Due to Observed Instability

    Zimmer Biomet is recalling 53 ROSA Surgical Devices because of observed instability. The devices are computer-controlled arms used in neurosurgery.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V752000·2017-11-22

    Entegra Recalls 2010-2011 RVs Due to Fire Extinguisher Defect

    Entegra is recalling 2010-2011 Aspire, Anthem, and Cornerstone RVs because the installed fire extinguishers may clog, require excessive force to activate, or have nozzles that detach.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, ASPIRE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18703·2017-11-22

    Goal Zero Recalls Solar Charging Stations Due to Impact Hazard

    Goal Zero is recalling Street Charge solar powered charging stations because a weld failure could cause the top post to fall, posing an impact hazard.

    Product
    Street Charge solar powered mobile device charging stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E071000·2017-11-22

    Prevost Recalls Commercial Bus Driver Seats Due to Stuck Seat Belt Buckles

    Prevost is recalling specific aftermarket commercial bus driver seats because the seat belt buckle may be stuck in the locked position, preventing the seat belt from latching.

    Product
    SEAT BELTS:FRONT:BUCKLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0338-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Almonds nationwide and in Bermuda because the product contains undeclared milk.

    Product
    Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch, 9 oz. Plastic Cup, 9 oz. Stand Up Plastic Pouch, 12 oz. Square Plastic Tub, 17 oz. Family Size Plastic Pouch. Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market…
    Category
    Food
    Distribution
    Distributed nationwide