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.

34926–34950 of 79559

  • HighFDA (Devices)·Z-2251-2019·2019-08-21

    BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw

    BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x85 due to a manufacturing flaw in the sterile barrier system. The devices were distributed in the US and internationally.

    Product
    Go-EZ Screw 6.5x85, Item Number 19665 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2272-2019·2019-08-21

    Siemens SOMATOM Confidence CT Systems Recalled for Software Safety Issues

    Siemens Medical Solutions is recalling SOMATOM Confidence CT systems due to four software issues that may cause scan aborts.

    Product
    SOMATOM Confidence, Model Number 10590100 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2269-2019·2019-08-21

    Siemens CT Systems Recalled for Software Issues Causing Scan Aborts

    Siemens is recalling SOMATOM Definition Edge CT systems due to four safety-related software issues in syngo.CT version VB10A that may result in scan aborts.

    Product
    SOMATOM Definition Edge, Model Number 10590000 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2279-2019·2019-08-21

    BD Vacutainer Fluoride Tubes Recalled Due to Missing Preservative Additive

    Becton Dickinson is recalling 247,000 blood alcohol test tubes because they lack the required fluoride additive, which may cause inaccurate test results if samples are stored for more than two days.

    Product
    BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number: 367001 Product Usage: Blood Alcohol determinations
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2274-2019·2019-08-21

    Siemens SOMATOM Force CT Systems Recalled for Software Scan Abort Issues

    Siemens Medical Solutions is recalling SOMATOM Force CT systems due to four software issues that may cause scan aborts.

    Product
    SOMATOM Force, Model Number 10742326 - Product Usage: Computed tomography systems intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by the system can be used by a trained physician as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2255-2019·2019-08-21

    BioPro Go-EZ Screw Recalled Due to Sterile Barrier Manufacturing Flaw

    BioPro, Inc. is recalling 2 units of Go-EZ Screw 6.5x105 (Item 19669) due to a manufacturing flaw in the sterile barrier system.

    Product
    Go-EZ Screw 6.5x105, Item Number 19669 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1990-2019·2019-08-21

    Entenmann's Little Bites Cookies Recalled for Possible Plastic Pieces

    BIMBO Bakeries USA Inc. is recalling 160,000 boxes of Entenmann's Little Bites Soft Baked Cookies due to a manufacturing failure that may have introduced small plastic pieces into the product.

    Product
    Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Chip variety) Net Weight of 5ct box 6.88oz. 5 pouches per package, package type is carton, units per case 12
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-1997-2019·2019-08-21

    Kerry Batter Mix Recalled for Nylon String Foreign Material

    Kerry, Inc. is recalling 4,765 bags of Batter Mix due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.

    Product
    Batter Mix, Item Number 30753149.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2249-2019·2019-08-21

    BioPro Go-EZ Screw Recalled Due to Sterile Barrier Flaw

    BioPro, Inc. is recalling 4 units of Go-EZ Screw 6.5x95 due to a manufacturing flaw in the sterile barrier system.

    Product
    Go-EZ Screw 6.5x95, Item Number 19667 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2275-2019·2019-08-21

    NeuroLogica HS70A Ultrasound Systems Recalled for Probe Overheating Risk

    NeuroLogica is recalling HS70A Diagnostic Ultrasound Systems due to a potential risk of probes overheating when users decrease the Doppler Sample Volume size in Doppler Only mode.

    Product
    HS70A Diagnostic Ultrasound System Version 2.01.00, 2.01.01, 2.01.02, 2.01.03, 2.01.04, 2.01.05, 2.01.06, 1.00.06, 1.00.07, 1.00.08, 1.00.09, 1.00.10, 1.00.11, 1.00.12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2239-2019·2019-08-21

    BioPro K-Wire HBS Sterile Recalled for Sterile Barrier Flaw

    BioPro, Inc. is recalling 17 units of K-Wire HBS Sterile due to a manufacturing flaw in the sterile barrier system.

    Product
    K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2258-2019·2019-08-21

    BioPro Go-EZ Screw Recalled for Sterile Barrier Manufacturing Flaw

    BioPro, Inc. is recalling 3 units of Go-EZ Screw 6.5x38 due to a manufacturing flaw in the sterile barrier system.

    Product
    Go-EZ Screw 6.5x38, Item Number 19655 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS System. It is intended for various orthopedic surgical procedures but is not intended for use in the spine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2276-2019·2019-08-21

    NeuroLogica WS80A Diagnostic Ultrasound System Recalled for Probe Overheating Risk

    NeuroLogica is recalling WS80A Diagnostic Ultrasound Systems because probes may overheat when users decrease the Doppler Sample Volume size in Doppler Only mode.

    Product
    WS80A Diagnostic Ultrasound System Version 1.00.16, 3.00.17, 3.00.18, 3.00.19, 3.01.00, 3.01.01, 3.01.02, 3.01.03, 3.01.04, 3.01.05, 3.01.06, 3.01.07, 3.01.08, 3.01.09, 4.00.08, 4.00.09, 4.00.10, 4.00.11, 4.01.00, 4.01.01, 4.01.02, 4.01.03, 4.01.04, 4.01.05, 4.01.06, 4.01.07…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2002-2019·2019-08-21

    Kerry Recalls CKN Fried Breader Due to Nylon String Foreign Material

    Kerry, Inc. is recalling 810 bags of CKN Fried CKN Breader because the product contains foreign material (nylon string). The product was distributed to manufacturers and food service distributors in nine US states.

    Product
    CKN Fried CKN Breader, Item Number 30753155.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2018-2019·2019-08-21

    Kerry Recalls Cajun Catfish Breader Due to Nylon String Foreign Material

    Kerry, Inc. is recalling 154 bags of Cajun Catfish Breader because the product contains foreign material, specifically nylon string.

    Product
    Cajun Catfish Breader, Item Number 30753193.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2041-2019·2019-08-21

    Kerry Sweet Onion Crusted Breader Recalled for Nylon String Foreign Material

    Kerry, Inc. is recalling Sweet Onion Crusted Breader due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.

    Product
    Sweet Onion Crusted Breader, Item Number 30753308.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2016-2019·2019-08-21

    Kerry Breader Mix Recalled for Nylon String Foreign Material

    Kerry, Inc. is recalling 104 bags of Breader Mix Non-Pho due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.

    Product
    Breader Mix Non-Pho, Item Number 30753191.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2021-2019·2019-08-21

    Kerry Spicy Breader Recalled for Nylon String Foreign Material

    Kerry, Inc. is recalling 160 bags of Spicy Breader due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine states.

    Product
    Spicy Breader, Item Number 30753198.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2003-2019·2019-08-21

    Kerry Breader Recalled for Nylon String Foreign Material

    Kerry, Inc. is recalling 1,470 bags of Breader containing nylon string. The product was distributed to manufacturers and food service distributors in nine states.

    Product
    Breader, Item Number 30753156.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2027-2019·2019-08-21

    Kerry CFS Breader Recalled for Nylon String Foreign Material

    Kerry, Inc. is recalling 642 bags of CFS Breader because the product contains foreign material (nylon string). The product was distributed to manufacturers and food service distributors in nine US states.

    Product
    CFS Breader, Item Number 30753213.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-2044-2019·2019-08-21

    Kerry Breader Recalled Due to Nylon String Foreign Material

    Kerry, Inc. is recalling 52 bags of Breader (Item 30753324.49) because the product contains nylon string. The product was distributed to manufacturers and food service distributors in nine US states.

    Product
    Breader, Item Number 30753324.49, Net Wt. 50 lb, Distributed by Kerry Ingredients & Flavours, Beloit, WI
    Category
    Food
    Distribution
    10 states