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.

57001–57025 of 79657

  • SevereCPSC·15213·2015-08-13

    Ambient Weather Recalls Radios Due to Fire Hazard

    Ambient Weather is recalling about 12,500 weather radios because the AC power adapter can overheat, posing a fire hazard. Consumers should stop using the radios and contact the company for a free replacement adapter.

    Product
    Ambient Weather radios
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V515000·2015-08-13

    Toyota Recalls 4Runners Due to Accessory Exhaust Tip Burn Risk

    Southeast Toyota Distributors is recalling 2010-2015 Toyota 4Runners because accessory exhaust tips may contact people and cause burns.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V513000·2015-08-13

    AEV Trauma Hawk Recalled for Reversed Backup Camera Images

    Halcore Group is recalling 2014-2015 AEV Trauma Hawk emergency vehicles because the backup camera may display reversed images, increasing crash risk.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2908-2015·2015-08-12

    Whole Foods Market Recalls Blackberry Pies Due to Undeclared Egg

    Whole Foods Market is recalling specific blackberry pies in Texas, Oklahoma, and Louisiana because they contain undeclared egg, a major food allergen.

    Product
    Blackberry Pie 9 Inch NET WT. 2lb 4oz (1021g) and Blackberry Pie Half NET WT. 1lb 1oz (482g) and individual slices.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-2907-2015·2015-08-12

    Whole Food Market Recalls Cherry Pies Due to Undeclared Egg

    Whole Food Market is recalling specific cherry pies because they contain undeclared egg. The recall covers products sold in Texas, Oklahoma, and Louisiana.

    Product
    Cherry Pie 9 Inch NET WT. 2lb 4oz (1021g) and Cherry Pie Half NET WT. 1lb 1oz (482g) and individual slices
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-2906-2015·2015-08-12

    Whole Food Market Recalls Peach Pies Due to Undeclared Egg

    Whole Food Market is recalling 11 units of peach pies in Texas, Oklahoma, and Louisiana because they contain undeclared egg.

    Product
    Peach Pie 9 Inch NET WT. 2lb 4oz (1021g) and Peach Pie Half NET WT. 1lb 1oz (482g) and individual slices
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-2916-2015·2015-08-12

    Whole Foods Market Recalls Raw Macadamia Nuts Due to Salmonella

    Whole Foods Market is recalling raw macadamia nuts found positive for Salmonella. The product was distributed in 12 states.

    Product
    Whole Foods Market Raw Macadamia Nuts NET WT 11 oz (312g). UPC: 0-76958-62059-1, Distributed by Whole Foods Market Austin, TX 78703
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Devices)·Z-2319-2015·2015-08-12

    Cook Inc. Recalls Slip-Cath Beacon Tip Catheters Due to Tip Separation

    Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because the tips may split or separate, potentially causing loss of function or complications.

    Product
    Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2943-2015·2015-08-12

    Anabolic Science Labs Recalls Slim X Lean Hour Energy Drink

    Anabolic Science Labs is recalling Slim X Lean Hour 12+ Hour Energy products due to undeclared synthetic hormone ingredients.

    Product
    "***SLIM X LEAN HOUR 12+ HOUR ENERGY***PRODUCT ID: ASL-SXL-03***Manufactured for: ASL ANABOLIC SCIENCE LABS WINTER PARK, FL 32789***
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1309-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Tri-Mix Injection Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling SIU-Tri-Mix 30/2/20 Injection in Oklahoma due to a lack of documentation proving proper environmental monitoring during production.

    Product
    SIU-Tri-Mix 30/2/20 Inj., Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1398-47
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2318-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Royal Flush Plus High-Flow Catheters

    Cook Inc. is recalling Beacon Tip Royal Flush Plus High-Flow Catheters due to reports of tip splits or separation that may cause loss of function or complications.

    Product
    Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1297-2015·2015-08-12

    Apothecary Shoppe Recalls SIU-Phent Injection Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling SIU-Phent .4 mg/PGE1 20 mcg/mL Injection due to a lack of documentation for environmental monitoring during production.

    Product
    SIU-Phent .4 mg/PGE1 20 mcg/mL Injection, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 99999-1802-97
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2325-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because adhesive failure may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9731754 - Passive Biopsy Fee Per Use (FPU) Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2326-2015·2015-08-12

    Aesculap S4C Occiput Torque Wrench Recalled Due to Reassembly Defect

    Aesculap is recalling 10 S4C Occiput Torque Wrenches because improper reassembly after reprocessing caused a screw to break during implantation.

    Product
    S4C Occiput Torque Wrench F/Set Screw; used to tighten the S4 Cervical Spinal System clamping screws with a defined torque 2.8 Nm for tightening the clamping screw in the screw head/hook head/occipital plate/transverse connector and other connectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2317-2015·2015-08-12

    Cook Inc. Recalls Beacon Tip Torcon NB Advantage Catheters

    Cook Inc. is recalling Beacon Tip Torcon NB Advantage Catheters due to reports of tip splits or separation, which may cause loss of function or complications.

    Product
    Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2324-2015·2015-08-12

    Medtronic Passive Biopsy Needle Kit Recalled for Adhesive Defect

    Medtronic is recalling 1,415 Passive Biopsy Needle Kits because compromised adhesive may cause the sphere assembly to move, leading to inaccurate navigation during brain biopsies.

    Product
    Medtronic Passive Biopsy Needle Kit, Part Number 9733068 - Passive Biopsy Needle Kit. The image guided Passive Biopsy Needle is an accessory instrument with the StealthStation System. The Biopsy Needle is intended to be used for stereotaxy biopsy of brain tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1296-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine and Phentolamine Injection Due to Sterility Concerns

    The Apothecary Shoppe is recalling specific lots of SIU-Papav/Phentol 30/1 mg/mL Injection due to a lack of documentation for environmental monitoring during production.

    Product
    SIU-Papav/Phentol 30/1 mg/mL Injection, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 99999-6830-10
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1295-2015·2015-08-12

    Apothecary Shoppe Recalls Papaverine and Phentolamine Injection Due to Sterility Concerns

    The Apothecary Shoppe LLC is recalling specific vials of Papaverine and Phentolamine Injection due to a lack of documentation confirming proper environmental monitoring during production.

    Product
    SIU-Papav/Phent 24/1 mg/mL Inj., Rx Only, 10 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1461-57
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-2939-2015·2015-08-12

    Wish-Bone Ranch Dressing Recalled for Undeclared Eggs

    Pinnacle Foods is recalling Wish-Bone Ranch Dressing because it contains undeclared eggs, posing a risk to consumers with egg allergies.

    Product
    Wish-Bone Ranch Dressing Net. Wt. 24 oz. Distributed by Pinnacle Foods Group USA LLC Cherry Hill, NJ 08003-3620 UPC 0-41321-00661-6
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Devices)·Z-2264-2015·2015-08-12

    Medtronic Recalls EnVeo R Loading Systems Due to Particulate Presence

    Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.

    Product
    EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular valve delivery system for use with the Medtronic CoreValve Evolut R system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V508000·2015-08-12

    Jeep Renegade Recall for Radio Software Vulnerability

    Chrysler is recalling 2015 Jeep Renegade vehicles to fix a radio software vulnerability that could allow unauthorized remote control of vehicle systems.

    Product
    JEEP — JEEP RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2327-2015·2015-08-12

    Titan Spine Recalls Endoskeleton Locking Bone Screw Assemblies

    Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assemblies because the locking collars are not locking.

    Product
    Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; 5302-3516 / 03.5 x 16mm Locking Screws; 502-3518 / 03.5 x 18mm…
    Category
    Medical Device
    Distribution
    8 states