The Recall Desk

State

Louisiana product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49126–49150 of 80793

  • HighFDA (Devices)·Z-1119-2017·2017-02-08

    Siemens Recalls IMMULITE PSA Kits Due to Negative Bias

    Siemens Healthcare Diagnostics is recalling IMMULITE PSA kits worldwide because patient samples show an average negative bias of approximately -22%.

    Product
    IMMULITE/IMMULITE 1000 Systems, Third Generation PSA, Catalog Number/REF LKUP1, SMN 10380956 (OUS Kit Catalog) Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers for the quantitative measurement of prostate-specific antigen (PSA) in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1365-2017·2017-02-08

    Rich Products Vanilla Ice Cream Cake Recalled for Undeclared Walnuts

    Rich Products Corp is recalling Signature SELECT Vanilla Ice Cream & White Cake ICE CREAM CAKE because it may contain undeclared walnuts.

    Product
    Signature SELECT Vanilla Ice Cream & White Cake ICE CREAM CAKE , NET WT 4 LB 13 OZ, KEEP FROZEN, UPC 021130 114641, Product Code 06620 ---
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1130-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling 185 units of Intact Disposable Wands because the sterile barrier was breached, compromising sterility.

    Product
    Intact Disposable Wands (part of the Intact System) 900-115: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1131-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall covers 320 units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 777-115: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0452-2017·2017-02-08

    Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures

    Dr. Reddy's Laboratories is recalling Flucanazole 200 mg tablets nationwide due to failed dissolution specifications and stability issues.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0451-2017·2017-02-08

    Dr. Reddy's Recalls Flucanazole Tablets Due to Dissolution Failures

    Dr. Reddy's Laboratories is recalling Flucanazole 150 mg tablets because they failed dissolution specifications and 18-month stability testing.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1109-2017·2017-02-08

    Immuno-Mycologics Recalls Cryptococcal Antigen Lateral Flow Assay Due to False Positives

    Immuno-Mycologics is recalling 630 units of the Cryptococcal Antigen Lateral Flow Assay because specific lots have lower specificity, leading to reported false positive results.

    Product
    Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Reference # CR2003
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1115-2017·2017-02-08

    Zimmer Biomet Recalls Vanguard Total Knee System Femoral Components Due to Labeling Errors

    Zimmer Biomet is recalling Vanguard Total Knee System femoral components because packaging labels may incorrectly identify the size or side of the implant.

    Product
    Vanguard Total Knee System Vanguard Open Box Femoral Components Item Number: 183100 Description: VNGD PS OPEN INTL FEM RT 55 Item Number: 183102 Description: VNGD PS OPEN INTL FEM-RT 57.5 Item Number: 183104 Description: VNGD PS OPEN INTL FEM RT 60 Item Number: 183106…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1114-2017·2017-02-08

    Zimmer Biomet Recalls Mislabelled Orthopedic Salvage System Tibial Bodies

    Zimmer Biomet is recalling 16 Orthopedic Salvage System tibial bodies because labels incorrectly identify them as AVL Modular Proximal Tibia components.

    Product
    Orthopedic Salvage System (OSS) 9cm prosthesis, knee, femorotibial, constrained, cemented, metal/polymer Knee System Tibial Bodies
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1117-2017·2017-02-08

    Ortho-Clinical VITROS Na+ Slides Recalled for Potential Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Na+ Slides because they may produce biased results if stored on the analyzer for 10 days after minimum warm-up.

    Product
    VITROS Na+ Slides, (UPN 10758750004812) For in vitro diagnostic use only. VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1118-2017·2017-02-08

    Siemens Mammomat Inspiration Mammography Systems Recalled for Software Error

    Siemens Medical Solutions USA is recalling 55 Mammomat Inspiration digital x-ray mammography systems due to a software error.

    Product
    Mammomat Inspiration full, field digital,system,x-ray,mammographic Product Usage: The Mammomat Inspiration system is intended for mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1427-2017·2017-02-08

    Roland Manzanilla Olives Stuffed With Anchovies Recalled for Microorganisms

    Roland Foods is recalling Manzanilla Olives Stuffed With Anchovies because FDA sampling found non-pathogenic Gram Positive Rods.

    Product
    Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES, DR. WT. 3 OZ. (85g), UPC Code: 41224714021 and Case UPC Code: 10041224714028, Item # 71402, PRODUCT OF SPAIN
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17732·2017-02-07

    Sony Expands Recall of VAIO Laptop Battery Packs for Fire Hazards

    Sony is expanding a recall of Panasonic lithium-ion battery packs used in VAIO laptops due to overheating risks that can cause burns and fires.

    Product
    Panasonic battery packs used in Sony Electronics laptop computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V074000·2017-02-07

    Cruiser RV Recalls 2016-2017 Boss Trailers Due to Furnace Exhaust Defect

    Cruiser RV is recalling 2016-2017 Boss recreational trailers because a vertically-mounted furnace may have exhaust ports at the top, creating an unsafe operating condition.

    Product
    CRUISER RV — CRUISER RV BOSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V070000·2017-02-03

    Volkswagen Recalls 2017 Jetta Vehicles Due to Engine Seizure Risk

    Volkswagen is recalling 2017 Jetta vehicles with 1.4L engines because the engine block may be improperly cast, potentially causing the engine to seize and leading to a loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V072000·2017-02-03

    REV Recalls 2016-2017 Motorhomes Due to Fuel Leak Risk

    REV Recreation Group is recalling 391 Holiday Rambler and Fleetwood motorhomes because a spring shackle bolt may puncture fuel components, creating a fire hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER XE, STORM, VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V071000·2017-02-03

    Midwest All-Poly 3000 Series Recalled for Brake Light Switch Defect

    Midwest Fire Equipment is recalling one 2017 All-Poly 3000 Series vehicle because the stop light switch may fail to illuminate brake lights, increasing crash risk.

    Product
    MIDWEST — MIDWEST ALL-POLY 3000 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V068000·2017-02-02

    Nissan Recalls 2002 Pathfinder and Infiniti QX4 for Air Bag Defect

    Nissan is recalling 2002 Pathfinder and Infiniti QX4 vehicles because the front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN QX4, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17081·2017-02-02

    Disney Recalls Mickey Mouse Nightlights Due to Fire Hazard

    Walt Disney Parks and Resorts is recalling Happy Holidays! Mickey Mouse Nightlights because liquid can leak onto electrical outlets, posing a fire hazard.

    Product
    Happy Holidays! Mickey Mouse Nightlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V067000·2017-02-02

    BMW Recalls 2011-2012 Models for Rear Driveshaft CV Joint Defect

    BMW is recalling specific 2011-2012 models because the rear driveshaft CV joint may break, causing loss of propulsion and increasing crash risk.

    Product
    BMW — BMW 335I, Z4, 335D, 535I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V066000·2017-02-02

    Jayco Recalls 2017 Seismic Fifth-Wheel Trailers Due to Brake Wiring Defect

    Jayco is recalling 2017 Seismic and Seismic Wave fifth-wheel trailers because improper wiring may prevent the breakaway switch from functioning, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC WAVE, SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1361-2017·2017-02-01

    Earth Balance Vegan Mac and Cheese Recalled for Undeclared Milk

    Boulder Brands is recalling Earth Balance Vegan Mac and Cheese products due to undeclared milk, a major allergen.

    Product
    Earth Balance Vegan White Cheddar flavored Mac and Cheese, 6oz package, Cardboard box/carton, 12 packages per distributed case, Ambient storage.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1065-2017·2017-02-01

    Villa Radiology Systems Recalls Apollo DRF X-Ray Systems Due to Injury Risk

    Villa Radiology Systems LLC is recalling 66 Apollo DRF multi-function x-ray systems because a chain of faults led to an injury involving inadvertent movement activation.

    Product
    Apollo DRF: Model: 9784220831 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    26 states