The Recall Desk

State

Louisiana product recalls

73,809 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,966
Critical
1,107
Severe
1,740
Most recent
2026-11-04

Of the 6,966 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 1,740 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43101–43125 of 80775

  • ModerateFDA (Devices)·Z-1049-2018·2018-03-21

    Zimmer Biomet Recalls Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling 13,227 CR-FLEX knee implants because LDPE packaging may leave residue on the polished surface.

    Product
    CR-FLEX PCT FEM C-R MINUS CR-FLEX PCT FEM D-L MINUS CR-FLEX PCT FEM D-R MINUS CR-FLEX PCT FEM E-L MINUS CR-FLEX PCT FEM E-R MINUS CR-FLEX PCT FEM F-L MINUS CR-FLEX PCT FEM F-R MINUS CR-FLEX PCT FEM G-L MINUS CR-FLEX PCT FEM G-R MINUS This device is indicated for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1036-2018·2018-03-21

    Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.

    Product
    LPS FEM COMP SZ B-L LPS FEM COMP SZ B-R LPS FEM COMP SZ C-L LPS FEM COMP SZ C-R LPS FEM COMP SZ D-L LPS FEM COMP SZ D-R LPS FEM COMP SZ E-L LPS FEM COMP SZ E-R LPS FEM COMP SZ F-L LPS FEM COMP SZ F-R LPS FEM COMP SZ G-L LPS FEM COMP SZ G-R This device is indicated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0979-2018·2018-03-21

    Zimmer Biomet Recalls Humeral Stems Due to Incorrect Lot Number Etching

    Zimmer Biomet is recalling 12 Humeral Stems because two lots were commingled and etched with incorrect lot numbers. The size difference is visually recognizable to the user.

    Product
    Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and revision total shoulder arthroplasty as well as hemi-arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2018·2018-03-21

    Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.

    Product
    CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP SIZE C/R CR OPTION FEM COMP SIZE D/L CR OPTION FEM COMP SIZE D/R CR OPTION FEM COMP SIZE E/L CR OPTION FEM COMP SIZE E/R CR OPTION FEM COMP SIZE F/L CR OPTION FEM COMP SIZE F/R CR OPTION FEM COMP SIZE G/L CR OPTION FEM COMP…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1044-2018·2018-03-21

    Zimmer Biomet Recalls LPS-FLEX Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling 13,227 LPS-FLEX knee implants because LDPE packaging may leave residue on the polished surface.

    Product
    LPS-FLEX PRECOAT FEMORAL B-R LPS-FLEX PRECOAT FEMORAL C-L LPS-FLEX PRECOAT FEMORAL C-R LPS-FLEX PRECOAT FEMORAL D-L LPS-FLEX PRECOAT FEMORAL D-R LPS-FLEX PRECOAT FEMORAL E-L LPS-FLEX PRECOAT FEMORAL E-R LPS-FLEX PRECOAT FEMORAL F-L LPS-FLEX PRECOAT FEMORAL F-R LPS-FLEX…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1039-2018·2018-03-21

    Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling specific hip and knee implants because LDPE packaging may leave residue on the polished surfaces.

    Product
    LPS PRECOAT SRF HDN FEM SZ D-L LPS PRECOAT SRF HDN FEM SZ D-R LPS PRECOAT SRF HDN FEM SZ E-L LPS POROUS SRF HDN FEM SZ D-LT LPS POROUS SRF HDN FEM SZ E-LT This device is indicated for patients with severe knee pain and disability
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2018·2018-03-21

    Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.

    Product
    CR-FLEX POR HATCP FEM C-L CR-FLEX POR HATCP FEM C-R CR-FLEX POR HATCP FEM D-L CR-FLEX POR HATCP FEM D-R CR-FLEX POR HATCP FEM E-L CR-FLEX POR HATCP FEM E-R CR-FLEX POR HATCP FEM F-L CR-FLEX POR HATCP FEM F-R CR-FLEX POR HATCP FEM G-L CR-FLEX POR HATCP FEM G-R This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1010-2018·2018-03-21

    Fresenius NaturaLyte Liquid Acid Concentrate Recalled for Potassium Concentration Error

    Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate because some units in the affected lot had a potassium concentration of 2.25 mEq/L instead of the labeled 2.0 mEq/L.

    Product
    NaturaLyte¿ Liquid Acid Concentrate 2.0 mEq/L, Model # 08-2251-0 3.43 liter bottle This concentrate is formulated to be used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney…
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1058-2018·2018-03-21

    Zimmer Biomet Recalls Knee Implants Due to Packaging Residue

    Zimmer Biomet is recalling 13,227 CR-FLEX knee implants because LDPE packaging may leave residue on the polished surface.

    Product
    CR-FLEX GSF PCT SZ C-R MINUS¿ CR-FLEX GSF PCT SZ D-L MINUS¿ CR-FLEX GSF PCT SZ D-R MINUS¿ CR-FLEX GSF PCT SZ E-L MINUS¿ CR-FLEX GSF PCT SZ E-R MINUS¿¿ CR-FLEX GSF PCT SZ F-L MINUS¿ CR-FLEX GSF PCT SZ F-R MINUS¿ CR-FLEX GSF PCT SZ G-L MINUS¿ CR-FLEX GSF PCT SZ G-R MINUS¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0939-2018·2018-03-21

    Zimmer Biomet Recalls Mislabeled Trabecular Metal Primary Hip Prostheses

    Zimmer Biomet is recalling 24 units of Trabecular Metal Primary Hip Prostheses due to mislabeling. The affected devices were distributed in the US and several international countries.

    Product
    Trabecular Metal¿ Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10) 63703649), and 2. 00-7864-013-20 (UDI: (01) 00889024139268 (17) 250731 (10) 63703681)
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0599-2018·2018-03-21

    Novel Laboratories Recalls Hydrocodone Bitartrate and Homatropine Methylbromide Tablets

    Novel Laboratories is recalling specific lots of Hydrocodone Bitartrate and Homatropine Methylbromide tablets due to failed impurities and degradation specifications.

    Product
    HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE — HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE (HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1057-2018·2018-03-21

    Zimmer Biomet Recalls NEXGEN GSF Porous Femoral LPS Flex Implants

    Zimmer Biomet is recalling NEXGEN GSF Porous Femoral LPS Flex implants because LDPE packaging may leave residue on the polished surface.

    Product
    NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F, RIGHT¿ " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0969-2018·2018-03-21

    Randox Recalls Immunoassay Premium Controls Due to Stability Claim Failure

    Randox Laboratories is recalling 117 kits of Immunoassay Premium Controls because the ACTH component does not meet the stated reconstituted stability claim in the product instructions for use.

    Product
    Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0936-2018·2018-03-21

    Medtronic Recalls Argyle Suction Tubing Due to Incorrect Packaging Labeling

    Medtronic is recalling 58,954 units of Argyle Suction Tubing because some pouches may be incorrectly labeled as Salem Sump Dual Lumen Stomach Tubes.

    Product
    Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0598-2018·2018-03-21

    Dr. Reddy's Recalls Clocortolone Pivalate Cream Due to Stability Issues

    Dr. Reddy's Laboratories is recalling Clocortolone Pivalate Cream, 0.1%, 90-gram tubes because viscosity failed stability specifications.

    Product
    Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Manufactured by: DPT, Laboratories Ltd. San Antonio, TX 78215, NDC 43598-341-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0589-2018·2018-03-21

    Psoriasin Daytime Relief Cream Recalled for Subpotent Coal Tar Content

    Alva-Amco Pharmacal Companies is recalling Psoriasin Daytime Relief Cream because it failed to maintain its label claim of coal tar throughout its expiry period.

    Product
    Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0970-2018·2018-03-21

    Randox Immunoassay Premium Plus Controls Recalled for Stability Issues

    Randox Laboratories is recalling Immunoassay Premium Plus Controls because the ACTH component does not meet the stability claims in the product instructions.

    Product
    Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2018·2018-03-20

    Mickey Brown Recalls Beef Burritos Produced Without Federal Inspection

    Mickey Brown, Inc. is recalling beef burrito products produced without federal inspection. No adverse reactions have been reported.

    Product
    Mickey Brown, Inc. — Mickey Brown, Inc Recalls Beef Burrito Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • HighCPSC·18127·2018-03-20

    Briggs & Stratton Recalls Riding Mowers Due to Reverse Mow Malfunction

    Briggs & Stratton is recalling Snapper, Simplicity, and Massey Ferguson riding mowers because a malfunctioning switch may allow the mower to mow while reversing, posing a risk of injury.

    Product
    Snapper, Simplicity, and Massey Ferguson riding mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V179000·2018-03-19

    Forest River Recalls Motorhomes Due to Power Steering Hose Fire Risk

    Forest River is recalling specific 2012-2017 motorhomes because an incorrectly routed power steering hose may rub against the starter motor, causing electrical arcing and a fire risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN, GLAVAL BUS CHARLESTON, BERKSHIRE, PATHFINDER, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V182000·2018-03-19

    McElrath Trailers Recalling 2013-2018 Models Due to Weld Failure Risk

    McElrath Trailers is recalling specific 2013-2018 models because a weld on the trailer neck may fail, potentially causing loss of control and a crash.

    Product
    MCELRATH TRAILERS — MCELRATH TRAILERS VX50-800, 818I, VX30-800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V181000·2018-03-19

    Entegra Aspire Recalled for Power Steering Hose Fire Risk

    Entegra Coach is recalling 2011-2012 and 2015-2016 Aspire motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.

    Product
    ENTEGRA — ENTEGRA ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V183000·2018-03-19

    REV Recalls 2018 Motorhomes Due to HVAC Fire Risk

    REV Recreation Group is recalling 600 2018 motorhomes because HVAC wires may disconnect, creating a fire risk if reconnected incorrectly.

    Product
    MONACO — MONACO, AMERICAN COACH, FLEETWOOD SIGNATURE, MARQUIS, AMERICAN REVOLUTION, AMERICAN DREAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18731·2018-03-19

    Carrier Recalls Commercial Rooftop HVAC Units Due to Fire Hazard

    Carrier is recalling about 530 commercial rooftop HVAC units because a humidifier fan may fail to shut off, posing a fire hazard. No injuries have been reported.

    Product
    Carrier WeatherExpert commercial packaged rooftop HVAC units with humidimizer option
    Category
    Consumer Product
    Distribution
    Distributed nationwide