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.

Which agencies issued them

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.

36326–36350 of 79560

  • SevereFDA (Drugs)·D-1289-2019·2019-05-29

    Heritage Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 50 mg because FDA testing found an impurity above acceptable levels.

    Product
    Losartan Potassium Tablets USP 50 mg 90 film coated tablets Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India. Manufactured for: Heritage Pharmaceuticals Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1383-2019·2019-05-29

    Beckman Coulter Recalls UniCel DxH 600 Hematology Analyzers for Platelet Errors

    Beckman Coulter is recalling 2,059 UniCel DxH 600 hematology analyzers because they may produce erroneously elevated platelet results without warning, potentially masking low platelet counts.

    Product
    UniCel DxH 600 Coulter Cellular Analysis System, REF number B23858. Product Usage: Note: The DxH 600 hematology analyzer is the same instrument as the DxH 800 (K140911), except that it is a benchtop unit with no instrument cart, computer stand, and no connectivity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1382-2019·2019-05-29

    Beckman Coulter UniCel DxH 800 Hematology Analyzer Recall for Platelet Errors

    Beckman Coulter is recalling UniCel DxH 800 analyzers because sporadic platelet results may be erroneously elevated without system flags, potentially leaving thrombocytopenia unrecognized.

    Product
    UniCel DxH 800 Coulter Cellular Analysis System, REF numbers 629029, B24465, B24802, B68304, B66445, and B63322. Product Usage: The UniCel DxH 800 Analyzer is a quantitative multi-parameter, automated hematology analyzer for in vitro diagnostic use in screening patient…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1291-2019·2019-05-29

    Heritage Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 25 mg because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium Tablets USP 25 mg 90 film coated tablets Rx Only Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India. Manufactured for: Heritage…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1310-2019·2019-05-29

    Integra LifeSciences Recalls MoniTorr CSF Drainage Systems Due to Stopcock Breakage

    Integra LifeSciences is recalling MoniTorr CSF Drainage Systems because the LimiTorr Transducer Mount and MoniTorr Panel Mount stopcocks may break.

    Product
    MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Valve MoniTorr 10102 10-102 CSF Drainage System w/Patient Line One Way Valve w MoniTorr 10110 10-110 CSF Drainage System used with Pole Mount System MoniTorr 10140 10-140 CSF Drainage System w/Vinyl Measuring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1287-2019·2019-05-29

    Heritage Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 50 mg because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium Tablets, USP 50 mg 1000 film coated tablets Rx Only Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India. Manufactured for: Heritage…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2019·2019-05-29

    J Deluca Fish Company Recalls Uninspected Frozen Yellow Walking Fish

    J Deluca Fish Company is recalling approximately 69,590 pounds of frozen Yellow Walking Fish imported from Vietnam without required import inspection.

    Product
    J Deluca Fish Company Inc. Recalls Siluriformes Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1384-2019·2019-05-29

    Beckman Coulter UniCel DxH 900 Hematology Analyzer Recall for Platelet Errors

    Beckman Coulter is recalling 341 UniCel DxH 900 hematology analyzers because they may produce erroneously elevated platelet results without warning, potentially masking low platelet counts.

    Product
    UniCel DxH 900 Coulter Cellular Analysis System, REF number C11478 Product Usage: Note: The DxH 900 hematology analyzer is CLIA categorized under document CR180294 and is currently marketed as a member of the instrument family of the DxH 800 cleared under K140911, per FDA s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1364-2019·2019-05-29

    Ortho-Clinical VITROS XT 7600 System Recalled for Potential Sample Dispensing Errors

    Ortho-Clinical Diagnostics is recalling VITROS XT 7600 Integrated Systems because sample fluid may be dispensed to incorrect positions, potentially causing erroneous assay results.

    Product
    VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW Product Code: 6844461 Product Usage: INTENDED USE: For in vitro diagnostic use only. The VITROS XT 7600 Integrated System is intended for use in the measurement of a variety of analytes of clinical interest
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1290-2019·2019-05-29

    Heritage Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium Tablets USP 100 mg 1000 film coated tablets Rx only Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India. Manufactured for: Heritage…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1381-2019·2019-05-29

    Dornier Diode Laser Fibers Recalled for Sterility Compromise

    Dornier Medtech America is recalling 400 units of Dornier Diode Laser Fibers due to pin hole package failures that compromise product sterility.

    Product
    Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K1001291 600 micron single use fiber K2011824 600 micron single use fiber K1001293 600 micron single use fiber K2011826 600 micron 5X reusable fiber K1008084 600 micron single use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2019·2019-05-29

    Oakworks Lithotripsy Table Recalled for Incorrect Actuator Assembly Error

    Oakworks Inc. is recalling three Lithotripsy/Urology Tables due to an assembly error involving incorrect actuators for lateral and longitudinal movements.

    Product
    OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are radiographic tables intended for use with mobile or compact stationary C-arm Imaging Systems. It is ideally suited for pain management imaging and therapeutic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1431-2019·2019-05-29

    Zimmer GmbH Recalls Osteofresh Arthrodesis Drills Due to Material Concerns

    Zimmer GmbH is recalling specific Osteofresh arthrodesis drills because they may have been manufactured from a material different from the specifications.

    Product
    Osteofresh arthrodesis drill, 2x70mm, center tip, AO, 10mm stop, Item Number 502015213
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1373-2019·2019-05-29

    Polymer Technology Systems Recalls CHOL+HDL+GLU Test Strips

    Polymer Technology Systems is recalling CHOL+HDL+GLU test strips because they may not fit tightly into the optical block, potentially causing incorrect results.

    Product
    CHOL+HDL+GLU test strips, REF 2412
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V401000·2019-05-29

    VCI Recalls Ambulances with Reversed Backup Camera Images

    VCI Emergency Vehicle Specialists is recalling ambulances where backup camera monitors may revert to factory settings, causing reversed images and increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, FORD C4500, E-450, F-450, redundant F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1488-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Orthopedic Screws Due to Material Concerns

    Zimmer GmbH is recalling specific cannulated orthopedic screws because they may have been manufactured from a material different from specifications.

    Product
    CBS high, countersink, cannulated, AO, Item Number ST503004542
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1371-2019·2019-05-29

    Polymer Technology Systems Recalls Lipid Panel Test Strips Due to Fit Issues

    Polymer Technology Systems is recalling Lipid Panel test strips because they may not fit tightly into the optical block, potentially causing incorrect results.

    Product
    Lipid Panel test strips, REF 1710, also private labeled under Henry Schein as REF 570-0414
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm AO Surgical Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 2.7mm AO surgical drills because they may be made from a different material than specified. The products were distributed to 41 US states.

    Product
    Drill for 2.7mm screw, 2x100mm, AO, Item Number ST502015208
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1463-2019·2019-05-29

    Zimmer V-TEK Cannulated AO Screws Recalled for Material Deviation

    Zimmer GmbH is recalling V-TEK standard-countersink cannulated AO screws because they may have been manufactured from a different material than specified.

    Product
    V-TEK", standard-countersink, cannulated, AO, Item Number 28.66.111
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1434-2019·2019-05-29

    Zimmer GmbH Recalls Stryker 3.5mm Screw Drills Due to Material Concerns

    Zimmer GmbH is recalling Stryker 3.5mm screw drills because they may have been manufactured from a different material than specified.

    Product
    Drill for 3.5mm screw, 2.5x125mm, stryker, Item Number 502015218
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1464-2019·2019-05-29

    Zimmer GmbH Recalls V-TEK Micro-Countersink Due to Material Concerns

    Zimmer GmbH is recalling V-TEK micro-countersinks because an investigation found they may be made from a different material than specified.

    Product
    V-TEK", micro-countersink, round shaft, Item Number 28.66.112
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1462-2019·2019-05-29

    Zimmer V-TEK Orthopedic Screws Recalled for Potential Material Deviation

    Zimmer GmbH is recalling V-TEK standard-countersink screws because they may have been manufactured from a different material than specified.

    Product
    V-TEK", standard-countersink, cannulated, round shaft, Item Number 28.66.110
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1455-2019·2019-05-29

    Zimmer GmbH Recalls CBS Micro Countersink Cannulated Round-Shaft Screws

    Zimmer GmbH is recalling CBS micro countersink cannulated round-shaft screws because they may be made from the wrong material.

    Product
    CBS micro, countersink, cannulated, round-shaft, Item Number 503004341
    Category
    Medical Device
    Distribution
    42 states