The Recall Desk

State

Oklahoma product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41051–41075 of 79563

  • HighFDA (Devices)·Z-2290-2018·2018-07-04

    RayStation Radiation Therapy Software Recalled for Dose Calculation Accuracy Issues

    RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software versions 6.0 through 7.0 because dose calculation accuracy may be less than expected in some situations.

    Product
    RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2318-2018·2018-07-04

    St Jude Medical Recalls Implantable Cardiac Devices for Security Firmware Update

    St Jude Medical is recalling implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2311-2018·2018-07-04

    Siemens Artis zee floor recall due to display failure

    Siemens is recalling 14 Artis zee floor systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation.

    Product
    Artis zee floor, Material no. 10094135, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2310-2018·2018-07-04

    Siemens Artis zee Ceiling Recalled for Display Malfunction

    Siemens is recalling 73 Artis zee ceiling units because the display may fail to show images after power save mode, potentially requiring procedure cancellation.

    Product
    Artis zee ceiling, Material no. 10094137, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2018·2018-07-04

    Siemens Artis Q.zen floor recall for display failure after power save

    Siemens is recalling Artis Q.zen floor units because the display may fail to show images after power save mode, potentially requiring procedure cancellation or patient transfer.

    Product
    Artis Q.zen floor, Material no. 10848353, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2306-2018·2018-07-04

    Siemens Artis Q.zeego X-ray System Display Malfunction Recall

    Siemens is recalling four Artis Q.zeego X-ray systems because the display may remain black after power save mode, preventing normal operation and requiring procedure cancellation or patient transfer.

    Product
    Artis Q.zeego, Material no. 10848283, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2329-2018·2018-07-04

    St Jude Medical Recalls Merlin PCS Programmer Firmware for Security

    St Jude Medical is releasing new firmware for Merlin PCS programmers to strengthen security against unauthorized access to cardiac devices.

    Product
    Merlin PCS programmer (Model # 3650), Software (Model # 3330)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2303-2018·2018-07-04

    Siemens Artis Q Biplane Recalled for Display Failure After Power Save

    Siemens is recalling five Artis Q biplanes because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.

    Product
    Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2315-2018·2018-07-04

    Toshiba Diagnostic Ultrasound Systems Recalled for Power Supply Defect

    Toshiba is recalling 162 Aplio I-series diagnostic ultrasound systems because the power supply unit may be damaged and fail to start up.

    Product
    Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may fail to start up when the power plug is inserted into a power outlet while the main power switch on the rear of the system is set to ON.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2309-2018·2018-07-04

    Siemens Artis zee Biplane MN Recalled for Display Failure

    Siemens is recalling two Artis zee biplane MN systems because the large display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.

    Product
    Artis zee biplane MN, Material no. 10094143, for angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2286-2018·2018-07-04

    Horiba Medical Recalls ABX Pentra Micro Albumin Reagents Due to Result Elevation

    Horiba Medical is recalling ABX Pentra Micro Albumin 2 CP reagents because they may produce elevated results if used immediately after a specific creatinine reagent.

    Product
    ABX Pentra Micro ALBUMIN 2 CP, Serum/Plasma, REF 1300032563 The device is intended for use in conjunction with certain materials to measure a variety of analytes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2319-2018·2018-07-04

    St Jude Medical Recalls Ellipse ICDs for Security Firmware Update

    St Jude Medical is recalling Ellipse ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access.

    Product
    Ellipse, Sterile EO, Model #/ Part #: CD1275-36/100116115; CD1275-36Q/100116116; CD1277-36/100048388, 100048391, 100060126, 100116208, 10011636; CD1277-36Q/100048374, 100048394, 100060198, 100098497, 100116268, 100116345; CD1293-36Q/100057838; CD1309-36/100057717…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2321-2018·2018-07-04

    St Jude Medical Recalls Fortify Assura ICDs for Security Firmware Update

    St Jude Medical is recalling Fortify Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.

    Product
    Fortify Assura, Sterile EO, Model #/ Part #: CD1257-40/100042322, 100059623; CD1257-40Q/100042341, 100059535; CD1259-40/100041914, 100042338, 100059536, 100059646, 100081567; CD1259-40Q/100041931, 100042339, 100059537, 100059620, 100059626, 100078685…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2326-2018·2018-07-04

    St Jude Medical Recalls Unify ICDs for Security Firmware Update

    St Jude Medical is recalling Unify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access.

    Product
    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1592-2018·2018-07-04

    Absonutrix Recalls Vitamin B12 Supplement Lacking Listed Ingredient

    Absonutrix is recalling Lyfetrition Vitamin B12 supplements because the product did not contain the vitamin listed on the label.

    Product
    Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as Methylcobalamyn) ABSONUTRIX 5500 Adams Farm Lane, Suite 206 Greensboro NC 27407 UPC 7 00443 88822 6
    Category
    Food
    Distribution
    22 states
  • HighNHTSA·18V444000·2018-07-03

    Forest River and Coachmen RVs Recalled for Power Window Fire Risk

    Forest River and Coachmen are recalling specific RV models because liquid leaks into the driver's power window switch, causing corrosion and increasing the risk of a fire.

    Product
    COACHMEN — COACHMEN, FOREST RIVER FREELANDER, LEPRECHAUN, CONCORD, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·058-2018·2018-07-02

    Nueske's Recalls Pork Products Due to Undeclared Ingredients

    Nueske's Meat Products is recalling approximately 12,946 pounds of braised pork products because they may contain undeclared brown rice flour and glycerin.

    Product
    Nueske's Meat Products, Inc. — Recall Notification Report 058-2018 (Pork Products)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·18750·2018-06-29

    BRP Recalls 2018 Can-Am ATVs Due to Fuel Leak and Fire Hazard

    BRP is recalling about 13,300 2018 Can-Am Outlander and Renegade ATVs because fuel can spray from the tank when opening the gas cap, posing a fire hazard.

    Product
    2018 Can-Am Outlander and Renegade all-terrain vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18751·2018-06-29

    Helmets R Us Recalls Rollerblade Helmets Due to Head Injury Risk

    Helmets R Us is recalling about 9,700 Rollerblade helmets sold to schools because they fail to meet federal safety standards, posing a risk of head injury.

    Product
    Rollerblade® helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V439000·2018-06-28

    BMW Recalls 2018 X5 and X6 Models for Front Control Arm Defect

    BMW is recalling 2018 X5 and X6 vehicles because a front lower-left control arm pivot bolt may not be properly hardened, potentially causing the arm to break and increasing crash risk.

    Product
    BMW — BMW X6, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide