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.

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.

41151–41175 of 79563

  • SevereFDA (Drugs)·D-0860-2018·2018-06-20

    Acne Shave Shave Cream Recalled for Potential Bacterial Contamination

    Shadow Holdings DBA Bocchi Labs is recalling Acne Shave Shave Cream due to CGMP deviations that may allow bacterial contamination.

    Product
    Acne Shave (salicylic acid) Shave Cream Acne Shield, 0.5%, 5.1 FL OZ (150 mL) tube, Distributed by: United Exchange Corp., 17311 Valley View Blvd, Cerritos, CA 90703 USA, UPC 7 80707 73111 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2213-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL XPP Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 5 boxes of RS 5F DL XPP Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL XPP KIT, Catalog Number 60M183104
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2214-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 104 boxes of RS 5F DL BIOFLO PASV kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M183481
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2205-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 2 boxes of RS 5F DL BIOFLO PASV kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M132324
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2222-2018·2018-06-20

    BioFlo PICC Nursing Kit Recalled for Unsafe Bacterial Endotoxin Levels

    Angiodynamics Inc. is recalling BioFlo PICC Nursing Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    BioFlo PICC (NV) 5FSL-55cm Maximal Barrier Nursing Kit w/ 70cm Nitinol Wire PG, Catalog Number 75-032
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0854-2018·2018-06-20

    PharMEDium Recalls Hydromorphone Syringes Due to Potency Issues

    PharMEDium Services is recalling 2,800 hydromorphone syringes nationwide because some units were found to be superpotent or subpotent.

    Product
    HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in 3 mL syringe, Rx, PharMEDium Services, LLC, Dayton, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0858-2018·2018-06-20

    FDA Recalls X-Jow Pain Gel Due to Potential Bacterial Contamination

    Shadow Holdings DBA Bocchi Labs is recalling X-Jow Pain Gel because CGMP deviations may have allowed bacterial contamination.

    Product
    X-Jow (menthol USP) Pain Gel, 1.25%, packaged in a) 4 oz. (113g) bottles (UPC 850547 00502 6) and b) 8 oz. (226g) bottles (UPC 8 50547 00503 3, Distributed by Herb-X Solutions, Inc., 3838 West Burbank Blvd., Burbank CA 91505.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2189-2018·2018-06-20

    Angiodynamics Recalls Bio-Stable Kits Due to Bacterial Endotoxin Risk

    Angiodynamics Inc. is recalling 50 boxes of Bio-Stable 5F kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, Catalog Number 45-818
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2216-2018·2018-06-20

    Angiodynamics Recalls RS TANDEM 5F DL BIOFLO PICC Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 15 boxes of RS TANDEM 5F DL BIOFLO PICC kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS TANDEM 5F DL BIOFLO PICC, Catalog Number 60M250097
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2221-2018·2018-06-20

    Angiodynamics Recalls BioFlo PICC Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling BioFlo PICC nursing kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kit PG, Catalog Number 75-019
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2211-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 11 boxes of RS 5F DL BIOFLO PASV kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M181578
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2208-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 7 boxes of RS 5F DL BIOFLO PASV kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M150373
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2188-2018·2018-06-20

    Angiodynamics Recalls XCELA PASV Nitinol Wire Kits Due to Endotoxin Risk

    Angiodynamics Inc. is recalling 7 boxes of XCELA PASV 5F SL 55CM IR-145 Nitinol Wire Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2220-2018·2018-06-20

    Angiodynamics Recalls Xcela Maximal Barrier Nursing Kits Due to Endotoxins

    Angiodynamics Inc. is recalling Xcela 5FDL-55cm Maximal Barrier Nursing Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    Xcela 5FDL-55cm Maximal Barrier Nursing Kit PG, Catalog Number 75-003
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2206-2018·2018-06-20

    Angiodynamics Recalls TANDEM 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling TANDEM 5F DL BIOFLO PASV kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    TANDEM 5F DL BIOFLO PASV, Catalog Number 60M140567
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2219-2018·2018-06-20

    Angiodynamics Recalls CAN 5F Dual Xcela PICC Kits for Endotoxin Risk

    Angiodynamics Inc. is recalling 27 boxes of CAN 5F Dual Xcela PICC kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    CAN 5F DUAL XCELA PICC, Catalog Number 60M701532
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-2181-2018·2018-06-20

    Siemens Recalls Dimension Gentamicin Flex Reagent Cartridges Due to Inaccuracy

    Siemens Healthcare Diagnostics is recalling specific lots of Dimension Gentamicin Flex reagent cartridges because they may produce inaccurate test results at the low end of the measurement range.

    Product
    Dimension Gentamicin Flex reagent cartridge, DM GENT, gentamicin enzyme immunoassay, Lot numbers affected are EB8115, BB8159, and FB8275.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2182-2018·2018-06-20

    Siemens Gentamicin Reagent Cartridge Recall Due to Low-End Inaccuracy

    Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista Gentamicin Flex reagent cartridges because they may produce inaccurate results at low concentrations.

    Product
    Dimension Vista Gentamicin Flex reagent cartridge, DV GENT, gentamicin enzyme immunoassay. Affected lots are 17135BC, 17150BF, 17159BD, 17178AC, 17269BD, and 17312BB.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2060-2018·2018-06-20

    Shimadzu Sonialvision Safire II X-ray System Recalled for Irradiation Display Error

    Shimadzu Medical Systems is recalling 17 Sonialvision Safire II angiographic x-ray systems because the irradiation time and integral dose displays may reset to zero during serial radiography.

    Product
    Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device intended to be used for the radiography in the hospital with X-ray devices. This device is operated and used by the physicians and X-ray technologist. The object of this device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2204-2018·2018-06-20

    Angiodynamics Recalls RS Tandem 5F DL Bioflo Pasv Catheters

    Angiodynamics Inc. is recalling RS Tandem 5F DL Bioflo Pasv catheters because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M120196
    Category
    Medical Device
    Distribution
    34 states
  • HighCPSC·18179·2018-06-20

    Werner Recalls Telescoping Aluminum Ladders Due to Fall Hazard

    Werner is recalling about 78,000 telescoping aluminum ladders because they can break while in use, posing a fall hazard.

    Product
    Multi-Purpose Telescoping Aluminum Ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide