The Recall Desk

State

Oklahoma product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53201–53225 of 79647

  • SevereFDA (Devices)·Z-1334-2016·2016-04-20

    Dexcom G4 Platinum Receiver Recall for Missing Audible Alarms

    Dexcom Inc is recalling G4 PLATINUM Receivers because they may fail to provide intended audible alarms or alerts to users.

    Product
    Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black; MT20649-PNK, Receiver (mg/dL), Pink; MT20649-BLU, Receiver (mg/dL), Blue. Intended to detect trends and track glucose patterns in persons with diabetes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1026-2016·2016-04-20

    Gold Medal Cincinnati Style Chili Recalled for Undeclared Milk

    Gold Medal Products is recalling 4 lb jars of Cincinnati Style Chili because the label failed to declare milk as an ingredient.

    Product
    #2473 CINCINNATI STYLE CHILI Savory Net Wt. 4 lbs (1.8kg) UPC 0 90939 12473 1 GOLD MEDAL PRODUCTS 10700 MEDALLION DRIVE CINCINNATI, OHIO 45241
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1047-2016·2016-04-20

    Figi's Classic Marzipan Recalled for Unlabeled Almond Content

    Figi's is recalling 8-ounce packages of Classic Marzipan because the product contains almonds that are not properly labeled on the ingredients list.

    Product
    Figi's Classic Marzipan, item 100-0034-200, 8 ounce
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1336-2016·2016-04-20

    Dexcom G4 PLATINUM Receiver Recall for Missing Audible Alarms

    Dexcom Inc is recalling G4 PLATINUM receivers because they may fail to provide intended audible alarms or alerts for diabetes patients.

    Product
    Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649 Receiver (mg/dL), Black. Intended to detect trends and track glucose patterns in persons with diabetes. The G4 PLATINUM CGM System and G4 PLATINUM (Professional) CGM System use the same receiver…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1338-2016·2016-04-20

    Dexcom G4 Platinum Pediatric Receiver Recall for Missing Audible Alarms

    Dexcom Inc is recalling 19,586 G4 Platinum Pediatric Receivers because they may fail to provide intended audible alarms or alerts.

    Product
    Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number: MT22608 Receiver (mg/dL), Black (pediatrics); MT22608-PNK, Receiver (mg/dL), Pink (pediatrics); MT22608-BLU, Receiver (mg/dL), Blue (pediatrics). Intended to detect trends and track glucose patterns in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V226000·2016-04-20

    StarTrans Senator II Transit Buses Recalled for Seat Separation Risk

    Forest River is recalling 2016 StarTrans Senator II transit buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.

    Product
    STARTRANS — STARTRANS SENATOR II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V227000·2016-04-20

    Starcraft Bus Recalls 2015-2016 Prodigy and Quest School Buses

    Forest River is recalling 2015-2016 Starcraft Prodigy and Quest school buses because seats may separate from the base frame due to bolt failure.

    Product
    STARCRAFT BUS — STARCRAFT BUS QUEST, PRODIGY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1064-2016·2016-04-20

    Chicken of the Sea Canned Tuna Recalled for Potential Undercooking

    Tri-Union Seafoods is recalling Chicken of the Sea canned tuna due to an equipment malfunction that may have caused the product to be undercooked.

    Product
    Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Oil, 48 cans per case, UPC code is 0 4800000195 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0887-2016·2016-04-20

    Morrison's Pancake Mix Recalled for Potential Metal Fragments

    Morrison's Pancake Mix is being recalled because it may contain small metal fragments from a wire mesh sifter.

    Product
    Morrison's Pancake Mix Complete Net Wt 5 LB (2.27 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V228000·2016-04-20

    Toyota 4Runner Recall for Inaccurate Load Carrying Capacity Label

    Gulf States Toyota is recalling 2015-2016 Toyota 4Runners with dealer-installed accessories because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.

    Product
    TOYOTA — TOYOTA 4RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1385-2016·2016-04-20

    Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risk

    Synthes (USA) Products LLC is recalling 289 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if a surgeon attempts to remove it.

    Product
    SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1382-2016·2016-04-20

    GE Healthcare Recalls Aisys Carestation Anesthesia Devices Due to Bolus Issue

    GE Healthcare is recalling Aisys Carestation anesthesia devices due to a potential safety issue involving a momentary, self-correcting anesthetic agent bolus when using 21% oxygen.

    Product
    GE Healthcare, Aisys Carestation.
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-1381-2016·2016-04-20

    GE Healthcare Recalls Aisys CS2 Anesthesia Devices Due to Bolus Issue

    GE Healthcare is recalling Aisys CS2 and upgraded Aisys anesthesia devices due to a potential safety issue involving a momentary, self-correcting anesthetic agent bolus when using 21% oxygen.

    Product
    GE Healthcare, Aisys CS2 anesthesia..
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-1383-2016·2016-04-20

    Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks

    Synthes (USA) Products LLC is recalling 212 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.

    Product
    SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1368-2016·2016-04-20

    ICU Medical Recalls Diana Automated Compounding Systems Due to Volume Accuracy Issues

    ICU Medical is recalling 47 Diana Automated Compounding Systems because they may not meet accuracy specifications when mixing volumes under 5ml.

    Product
    Diana Automated Compounding System, Final Assembly, Diana Onco Plus, Item No. CH5000, CH5000R The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1372-2016·2016-04-20

    Maquet Recalls HLS Set Advanced Oxygenator Tubing Packs Due to Endotoxin Risk

    Maquet Cardiovascular is voluntarily recalling HLS Set Advanced oxygenator tubing packs due to a potential risk of exposure to endotoxin.

    Product
    HLS Set Advanced with BIOLINE Coating Custom tubing packs for the oxygenator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1065-2016·2016-04-20

    Chicken of the Sea Recalls Canned Light Tuna Due to Undercooking Risk

    Tri-Union Seafoods is voluntarily recalling specific lots of Chicken of the Sea canned light tuna because an equipment malfunction may have resulted in undercooked product.

    Product
    Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Water, 48 cans per case, UPC code is 0 4800000245 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1377-2016·2016-04-20

    Intuitive Surgical Recalls da Vinci S Surgical System User Manuals

    Intuitive Surgical is recalling da Vinci S Surgical System user manuals because using non-approved instruments with ablation probes may increase microscopic metallic particulates.

    Product
    da Vinci S Surgical System (IS4000) user manual English and OUS. Product Usage: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1386-2016·2016-04-20

    Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks During Removal

    Synthes (USA) Products LLC is recalling 378 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures if a surgeon attempts to remove it.

    Product
    SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1363-2016·2016-04-20

    Natus Medical Recalls Medix NatalCare ST-LX Neonatal Incubators

    Natus Medical is recalling Medix NatalCare ST-LX neonatal incubators because defective hinge assemblies may cause ports to detach.

    Product
    Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1384-2016·2016-04-20

    Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks

    Synthes (USA) Products LLC is recalling 200 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.

    Product
    SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V229000·2016-04-20

    Jaguar Recalls XF Vehicles Due to Driver Air Bag Defect

    Jaguar is recalling certain 2009, 2011, 2012, and 2015 XF vehicles because the driver frontal air bag may deploy improperly, increasing injury risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1367-2016·2016-04-20

    ICU Medical Recalls Diana Automated Compounding System Due to Accuracy Issues

    ICU Medical is recalling 4 units of the Diana Automated Compounding System because compounded volumes under 5ml may not meet accuracy specifications.

    Product
    Diana Automated Compounding System, Diana Onco 3xx, Item No. ASN303 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1366-2016·2016-04-20

    ICU Medical Recalls Diana Automated Compounding System Due to Accuracy Issues

    ICU Medical is recalling 3 units of the Diana Automated Compounding System because compounded volumes under 5ml may not meet accuracy specifications.

    Product
    Diana Automated Compounding System, Diana Onco Plus 1.3, Item No. ASN223 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide