The Recall Desk

State

Oklahoma product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34576–34600 of 79559

  • SevereFDA (Devices)·Z-2315-2019·2019-09-18

    Teleflex Recalls Hudson RCI Sheridan Uncuffed Tracheal Tubes

    Teleflex Medical is recalling Hudson RCI Sheridan Uncuffed tracheal tubes because specific lots of the 15 mm connector may disconnect from the tube, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan Uncuffed: a) 2.0 mm, REF 5-10404 b) 2.5 mm, REF 5-10405 c) 3.0 mm, REF 5-10406 d) 3.5 mm, REF 5-10407 e) 4.0 mm, REF 5-10408 f) 4.5 mm, REF 5-10409 g) 5.0 mm, REF 5-10410 h) 5.5 mm, REF 5-10411 i) 6.0 mm, REF 5-10412 j) 6.5 mm, REF 5-10413 k) 7.0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·19206·2019-09-18

    Kichler Elan Shayla Mini Pendant Lights Recalled for Fire Hazard

    Kichler Lighting is recalling Elan Shayla Mini Pendant Lights because the sockets can overheat and catch fire. Consumers should stop using the fixtures and contact Kichler for a free replacement.

    Product
    Elan Shayla Mini Pendant Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2465-2019·2019-09-18

    Allergan Textured Breast Implants Recalled Due to Lymphoma Risk

    Allergan is recalling textured breast implants worldwide due to an increased risk of anaplastic large cell lymphoma (BIA-ALCL). Patients should consult their healthcare providers.

    Product
    Natrelle 150 Full Height and Short Height Implants, BIOCELL, INTRASHIEL, BioDIMENSIONAL Breast Implant, Styles 150 FH and 150 SH. Product Usage: Breast augmentation and Breast reconstruction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V664000·2019-09-18

    Subaru Recalls 2020 Legacy and Outback for Brake Pedal Bolt Issue

    Subaru is recalling 2020 Legacy and Outback vehicles because a missing or loose brake pedal bolt may reduce braking performance and increase crash risk.

    Product
    SUBARU — SUBARU LEGACY, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2313-2019·2019-09-18

    Teleflex Recalls Sheridan EZ-ENDO Tracheal Tubes Due to Disconnection Risk

    Teleflex Medical is recalling specific lots of Sheridan EZ-ENDO tracheal tubes because the 15 mm connector may disconnect, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-22515 e) 8.0 mm, REF 5-22516 f) 8.5 mm, REF 5-22517 g) 9.0 mm, REF 5-22518 h) 6.0 mm, REF 5-22512 i) 6.5 mm, REF 5-22513 Product Usage: Tracheal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2461-2019·2019-09-18

    Allergan Recalls Textured Breast Implants Due to Lymphoma Risk

    Allergan is recalling 4 million textured breast implants and tissue expanders worldwide due to an increased risk of anaplastic large cell lymphoma.

    Product
    Natrelle 510, TruForm, Dual-Gel, BIOCELL, Styles LX, MX, FX Product Usage: Breast augmentation and Breast reconstruction
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2318-2019·2019-09-18

    Teleflex Recalls Sheridan/HVT Novaplus Tracheal Tubes Due to Disconnection Risk

    Teleflex Medical is recalling specific lots of Sheridan/HVT Novaplus tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.

    Product
    Sheridan/HVT Novaplus: a) 7.0 mm, REF V5-10314 b) 7.5 mm, REF V5-10315 c) 8.0 mm, REF V5-10316 d) 8.5 mm, REF V5-10317 Product Usage: Tracheal tube/airway management
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V665000·2019-09-18

    Mercedes-Benz and Freightliner Sprinter Recalled for Hood Latch Defect

    Daimler Vans USA is recalling 2018-2019 Sprinter vans because an improperly tightened hood screw may allow the hood to open while driving, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 4500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2316-2019·2019-09-18

    Teleflex Medical Recalls Hudson RCI Sheridan/HVT Tracheal Tubes

    Teleflex Medical is recalling specific lots of Hudson RCI Sheridan/HVT tracheal tubes because the 15 mm Sheridan connector may disconnect from the tube, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF 5-10312 d) 6.5 mm, REF 5-10313 e) 7.0 mm, REF 5-10314 f) 7.5 mm, REF 5-10315 g) 8.0 mm, REF 5-10316 h) 8.5 mm, REF 5-10317 i) 9.0 mm, REF 5-10318 j) 10.0 mm, REF 5-10320 Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2454-2019·2019-09-18

    Allergan Recalls Textured Breast Implants Due to Lymphoma Risk

    Allergan PLC is recalling specific textured breast implants and tissue expanders due to a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).

    Product
    Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate Profile, Sterile, for the following style numbers: Style 110:110-090, 110-120, 110-150, 110-180, 110-210, 110-240, 110-270, 110-300, 110-330, 110-360, 110-390, 110-420, 110-450, 110-480…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2312-2019·2019-09-18

    Teleflex Medical Recalls Hudson RCI Sheridan/CF Tracheal Tubes

    Teleflex Medical is recalling Hudson RCI Sheridan/CF tracheal tubes because specific lots of the 15 mm Sheridan connector may disconnect from the endotracheal tube, potentially causing insufficient oxygenation.

    Product
    Hudson RCI Sheridan/CF: a) 3.0 mm, REF 5-10106, REF 5-10206 b) 3.5 mm, REF 5-10107 c) 4.0 mm, REF 5-10108, REF 5-10208 d) 4.5 mm, REF 5-10109 e) 5.0 mm, REF 5-10110, REF 5-10210 f) 5.5 mm, REF 5-10111 g) 6.0 mm, REF 5-10112, REF 5-10212 h) 6.5 mm, REF 5-10113, REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2156-2019·2019-09-18

    Krasnyi Oktyabr Recalls Dried Quince for Undeclared Sulfites

    Krasnyi Oktyabr Inc. USA is recalling 740 units of TAINY VOSTOKA Assorted Dried Fruits - Quince because the product contains undeclared sulfites.

    Product
    TAINY VOSTOKA ASSORTED DRIED FRUITS - QUINCE packaged in 500gram (17.65oz), clear plastic package marked with container code #24 02 2019 SS. The text on the package is written in Russian.
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2516-2019·2019-09-18

    Zimmer Biomet Recalls XP-XP Tibial Tray Due to Locking Bar Issue

    Zimmer Biomet is recalling 86 units of the XP-XP Tibial Tray because the locking bar may not fully engage. The recall covers units distributed across the US and several international regions.

    Product
    XP-XP Tibial Tray - Interlok 91mm Item # 195761
    Category
    Medical Device
    Distribution
    44 states
  • SevereFDA (Devices)·Z-2458-2019·2019-09-18

    Allergan Recalls McGhan Tissue Expanders Due to Lymphoma Risk

    Allergan is recalling McGhan Croissant-Shaped Tissue Expanders because the FDA identified a higher incidence of anaplastic large cell lymphoma in patients with textured breast implants.

    Product
    McGhan Croissant-Shaped Tissue Expanders, Style 134 Product Usage: intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2519-2019·2019-09-18

    Zimmer Biomet Recalls XP-XP Tibial Trays Due to Locking Bar Defect

    Zimmer Biomet is recalling specific XP-XP Tibial Trays because the locking bar may not fully engage. The recall covers units distributed in the US and several international regions.

    Product
    XP-XP Tibial Tray - Interlok 79 mm Item # 195758
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2126-2019·2019-09-18

    Bubbies Mochi Ice Cream Recalled for Potential Plastic Contamination

    Bubbies is recalling Mochi Ice Cream and related products due to the potential for free-floating foreign plastic pieces in the product.

    Product
    Bubbies Mochi Ice Cream -Chocolate Coconut Item Code CS812067, UPC Code 20203-5, UPC GTIN 10787325202032. Product is packed in oriented polystyrene sheet (OPS) thermo-formed 6-cavity trays, tray is packed in 6 count boxes.
    Category
    Food
    Distribution
    Distributed nationwide