The Recall Desk

State

Louisiana product recalls

73,741 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,965
Critical
1,107
Severe
1,739
Most recent
2026-10-28

Of the 6,965 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,739 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36876–36900 of 80706

  • 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
    FORD — FORD, CHEVROLET E-450, F-450, redundant F-250, E-350
    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
  • HighFDA (Devices)·Z-1416-2019·2019-05-29

    Zimmer GmbH Recalls 15mm Surgical Drills Due to Material Concerns

    Zimmer GmbH is recalling 15mm surgical drills that may have been manufactured from incorrect materials. The products were distributed to 41 US states.

    Product
    Drill, 15mm stop, 1x76mm, AO , Item Number 502015115
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1412-2019·2019-05-29

    Elekta Recalls Leksell GammaPlan 11.1 Software Due to Margin Overestimation

    Elekta Instrument AB is recalling Leksell GammaPlan 11.1 software because the margin tool overestimates treatment margins in certain areas.

    Product
    Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based system designed for Leksell Gamma Knife treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

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

    Product
    Drill, cannulated, 4x90mm, round shaft, Item Number 502015640
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1388-2019·2019-05-29

    Stryker Visum LED Surgical Lighting System Component Recall

    Stryker is recalling 3,176 EDS Light Suspension components for the Visum LED Surgical Lighting System due to a potential assembly defect in the joint.

    Product
    EDS Light Suspension, Central Axis, a component of the Stryker Visum LED Surgical Lighting System, with the following catalog numbers: 0682001286, EDS Light Suspension, Central Axis, 5P/FP; 0682001298, EDS Light Suspension, Central Axis, 5P; 0682001299, EDS Light Suspension…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1418-2019·2019-05-29

    Zimmer GmbH Recalls 26mm Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling 26mm orthopedic drills that may have been manufactured from a different material than specified.

    Product
    Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015124
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1454-2019·2019-05-29

    Zimmer GmbH Recalls MaxiCan 4.5 Countersink Due to Material Concerns

    Zimmer GmbH is recalling MaxiCan 4.5 countersinks because they may be made from a different material than specified. The products were distributed to 40 US states.

    Product
    MaxiCan 4.5 countersink, cannulated, AO, Item Number 503004177
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1458-2019·2019-05-29

    Zimmer CBS 4.0 Countersink Recalled for Material Specification Deviation

    Zimmer GmbH is recalling CBS 4.0 countersinks because they may have been manufactured from a material different from the defined specifications.

    Product
    CBS 4.0 countersink, cannulated, 15mm stop, AO, Item Number 503004352
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1448-2019·2019-05-29

    Zimmer GmbH Recalls V-TEK IVP Step Drills Due to Material Concerns

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

    Product
    V-TEK", IVP step drill 2.5-3.9x124mm, 16mm stop, contra-angle, Item Number 502015637
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1486-2019·2019-05-29

    Zimmer GmbH Recalls Contra-Angle Drills Due to Material Concerns

    Zimmer GmbH is recalling contra-angle drills that may have been manufactured from a different material than specified.

    Product
    Drill, contra-angle, 1.5x85mm, Item Number ST502015706
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1430-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling 2.7mm orthopedic drills because they may be made from a different material than specified. The products were distributed to 40 US states.

    Product
    Drill for 2.7mm screw, 2x120mm, AO, Item Number 502015212
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1466-2019·2019-05-29

    Zimmer V-TEK Cannulated AO Screws Recalled for Material Specification Deviation

    Zimmer GmbH is recalling V-TEK standard-countersink, cannulated, AO screws because they may have been manufactured from a material different from the defined specifications.

    Product
    V-TEK", standard-countersink, cannulated, AO, Item Number ST28.66.111
    Category
    Medical Device
    Distribution
    42 states