The Recall Desk

State

Oklahoma product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36876–36900 of 79560

  • ModerateFDA (Devices)·Z-1158-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Error

    Integra LifeSciences Corp. is recalling Tibial Total Ankle Prosthesis Trays because the labels list an incorrect metallic coating material symbol.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 0, Product No. LJU220T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1152-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Right, Part No. LJU202T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1167-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Flat Cut, Size 3, Right, Product No. LJU813T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1161-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Error

    Integra LifeSciences Corp. is recalling Tibial Total Ankle Prosthesis Trays because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1162-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling 2,029 Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Flat Cut, Size 1, Left, Product No. LJU821T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1136-2019·2019-04-24

    Ethicon Recalls VICRYL and PDS Sutures Due to Labeling Mismatches

    Ethicon, Inc. is recalling VICRYL, VICRYL Plus, and PDS sutures because the product inside may not match the sales unit carton and foil label.

    Product
    PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Sutures are intended for use in soft tissue approximation, including use in pediatric cardiovascular tissue where growth is expected to occur and ophthalmic surgery. PDS II suture is not indicated in adult cardiovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1155-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels incorrectly identify the metallic coating material.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 1, Left, Part No. LJU211T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1156-2019·2019-04-24

    Integra Salto Talaris Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Salto Talaris and Integra XT Revision ankle prostheses because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Left, Part No. LJU212T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1151-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris and Integra XT Revision ankle prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Salto Talaris Tibial Ankle Prosthesis Tray, Talar Dome, Size 1, Right, Part No. LJU201T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1157-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Left, Part No. LJU213T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1134-2019·2019-04-24

    Ethicon Recalls VICRYL Sutures Due to Labeling Mismatch

    Ethicon, Inc. is recalling VICRYL, VICRYL Plus, and PDS sutures because the product may not match the sales unit carton and foil label.

    Product
    VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 4-0 UND VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM) 2-0 VIO VICRYL CT VIO 8X18IN 0 S/A CT-1 CR VICRYL SUTURE 18"(45CM) 1 VIO VCL CT UD 8X18IN 2-0 S/A CP-2 CR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1301-2019·2019-04-24

    ConAgra Recalls Hunts Tomato Paste Cans Due to Potential Mold

    ConAgra Foods is recalling 145,380 cans of Hunts Tomato Paste No Salt Added due to potential mold caused by can damage.

    Product
    Hunts Tomato Paste No Salt Added 6 ounce cans, 12 per wholesale tray Can UPC: 2700038807 Tray UPC: 2700038809
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1140-2019·2019-04-24

    Philips Medical Systems Recalls Foot Switches for Imaging Systems

    Philips Medical Systems is recalling 7,209 foot switches used with specific imaging systems because bent pedals may prevent live fluoroscopy images or exposures.

    Product
    Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The Allura Xper FD Series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1164-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences Corp. is recalling Talar Dome Total Ankle Prostheses because the labels list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 3, Left, Product No. LJU823T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1149-2019·2019-04-24

    MedComp Recalls Hemodialysis Catheter Kits Due to Labeling Error

    Medical Components, Inc. is recalling 6,830 hemodialysis catheter insertion kits because the tray labels incorrectly identify the included introducer as valved when it is non-valved.

    Product
    14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-1195-2019·2019-04-24

    Siemens syngo Lab Data Manager System Recalled for Software Issues

    Siemens Healthcare Diagnostics is recalling 449 syngo Lab Data Manager systems due to software issues. The recall covers systems distributed in the US and nine other countries.

    Product
    syngo Lab Data Manager System - Product Usage: syngo Lab Data Manager is a clinical system that assists medical laboratory professions with pre-analytic and post-analytic functions. It works in conjunction with multiple instruments, the laboratory information system (LIS) and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1163-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Left, Product No. LJU822T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1170-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1194-2019·2019-04-24

    Roche Albumin BCP Reagent Recalled for Calibration Failures and QC Imprecision

    Roche Diagnostics is recalling 774 units of Albumin BCP reagent due to calibration failures and QC imprecision caused by elevated pH levels.

    Product
    Albumin BCP Product Usage: ALBP is an in vitro test used for the quantitative determination of albumin in human serum and plasma on Roche/Hitachi cobas c systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1124-2019·2019-04-24

    InvaGen Recalls Testosterone Cypionate Injection Due to Particulate Matter

    InvaGen Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because of the presence of particulate matter. The affected vials were distributed nationwide.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1165-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 1, Right, Product No. LJU811T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1172-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Left, Product No. LJV190T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1153-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Right, Part No. LJU203T
    Category
    Medical Device
    Distribution
    26 states