The Recall Desk

State

Louisiana product recalls

73,833 recalls have nationwide distribution and so reach Louisiana. 6,967 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,967
Critical
1,107
Severe
1,740
Most recent
2026-11-14

Of the 6,967 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 6,967 recalls whose distribution notice names Louisiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53651–53675 of 80800

  • CriticalFDA (Devices)·Z-1614-2016·2016-05-25

    Monteris Medical Recalls NeuroBlate Laser Probes Due to Lens Fracture

    Monteris Medical Corp is recalling 121 NeuroBlate System SideFire Select 2.2 mm Directional Laser Probes because a sapphire lens fractured during a procedure, introducing CO2 into a patient's brain.

    Product
    NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS000-01,SFS002-01, SFS122-01, SFS222-01, SFS322-01, SFS422-01, and SFS522-01. NeuroBlate System SideFire Select Directional Laser Probes are part of the NeuroBlate System. The Monteris…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1359-2016·2016-05-25

    Sugarfina Chocolate Malt Balls Recalled for Undeclared Peanuts

    Sugarfina, LLC is recalling Chocolate Malt Balls because they contain undeclared peanuts, a major food allergen.

    Product
    Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
    Category
    Food
    Distribution
    25 states
  • SevereNHTSA·16V359000·2016-05-25

    Subaru and Saab Recall Vehicles for Air Bag Inflator Rupture Risk

    Subaru is recalling specific 2003-2008 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V358000·2016-05-25

    Subaru and Saab Recall for Passenger Air Bag Inflator Rupture Risk

    Subaru is recalling specific 2003-2011 models and 2006 Saab 9-2x vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0855-2016·2016-05-25

    Renovo Patch Recalled for Lack of Approval and Subpotency

    TMIG Inc is recalling Renovo Patch because it was marketed without FDA approval and three lots were found to be subpotent.

    Product
    Renovo Patch (Capsaicin, 0.0375%, Menthol, USP 5.00%), 3-count patches per carton, Rx only, Distributed By: TMIG Inc, Marietta , GA 30062, Manufactured By: Pocono Coated Products LLC., Cherryville, NC 28021 NDC: 69176-025-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V361000·2016-05-25

    Subaru Recalls 2003-2004 Models for Air Bag Inflator Rupture Risk

    Subaru is recalling 2003-2004 Legacy, Outback, and Baja vehicles because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    SUBARU — SUBARU BAJA, OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V364000·2016-05-25

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Rupture Risk

    BMW is recalling specific 2007-2011 X5 and X6 models because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    BMW — BMW X5, X6 ACTIVEHYBRID SAC, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1680-2016·2016-05-25

    Zimmer Herbert Cannulated Bone Screw Recall for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling specific lots of Herbert Cannulated Bone Screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 mm Length 47115504507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 75 mm Length 47115507507 Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 90 mm Length 47115509007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16174·2016-05-25

    TJX Recalls Foldable Lounge Chairs Due to Risk of Injury

    TJX is recalling about 5,200 foldable lounge chairs sold at T.J. Maxx and Marshalls because they can collapse unexpectedly, posing a fall and injury hazard.

    Product
    Foldable lounge chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1677-2016·2016-05-25

    Zimmer Manufacturing Recalls Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded, 12 mm Length 47484001200 4.0 mm Cancellous Screw Fully Threaded, 14 mm Length 47484001400 4.0 mm Cancellous Screw Fully Threaded, 16 mm Length 47484001600 4.0 mm Cancellous Screw Fully Threaded, 18 mm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1678-2016·2016-05-25

    Zimmer Manufacturing Recalls Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling specific lots of sterile Hip and Trauma Implant Screws because a small hole may be present in the inner tray.

    Product
    M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 70 mm Length 00225307042
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V360000·2016-05-25

    Forest River Stealth Evo Recalled for Incorrect Tire Load Range

    Forest River is recalling 2016 Stealth Evo trailers because incorrect tires may fail prematurely, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1690-2016·2016-05-25

    Becton Dickinson Recalls Shielded IV Catheters Due to Defect

    Becton Dickinson is recalling 1.3 million shielded IV catheters because a defect could cause the catheter to separate or break.

    Product
    1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog number 381700 2) 24 G x 0.56 in. BD Angiocath-N" Autoguard" shielded IV catheter (0.7 mm x 14 mm) made of FEP polymer catalog number 381720
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2016·2016-05-25

    Zimmer 3.5 mm Cortical Screws Recalled for Potential Sterility Compromise

    Zimmer Manufacturing B.V. is recalling specific lots of 3.5 mm Cortical Screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping, 10 mm Length 47483501001 3.5 mm Cortical Screw SelfTapping, 14 mm Length 47483501401 3.5 mm Cortical Screw SelfTapping, 16 mm Length 47483501601 3.5 mm Cortical Screw SelfTapping, 24 mm Length 47483502401…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V355000·2016-05-25

    Grand Design RV Recalls 2016-2017 Trailers Due to Propane Leak Risk

    Grand Design RV is recalling 2016-2017 Imagine and Reflection trailers because a propane regulator defect may cause gas leaks and fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION, IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1371-2016·2016-05-25

    Nice! Peach Slices Recalled for Potential Glass Contamination

    MW Polar Foods is recalling Nice! Peach Slices and Mixed Fruit in 8-ounce jars due to potential glass in the product.

    Product
    Sliced Peaches (In Light Syrup), Net Wt. 8oz (227g), Bottle Label UPC 0-49022-80894-2, Case UPC 100-49022-80894-9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2016·2016-05-25

    Zimmer VersaFx Femoral Fixation System Screws Recalled for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling specific lots of VersaFx Femoral Fixation System screws because a small hole may be present in the inner tray, potentially compromising sterility.

    Product
    VersaFx Femoral Fixation System Hex head compression screw 4.7 mm dia. 2 inch (51 mm) length 47116202400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16746·2016-05-25

    Honda Recalls Mini Tillers Due to Throttle Cable Injury Risk

    Honda is recalling about 219,000 mini tillers because a pinched throttle cable can cause the tines to rotate unexpectedly, posing a risk of serious injury.

    Product
    Mini Tillers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1676-2016·2016-05-25

    Zimmer Manufacturing Recalls Specific Lots of Sterile Hip and Trauma Implant Screws

    Zimmer Manufacturing B.V. is recalling 99 units of sterile Hip and Trauma Implant Screws due to a potential small hole in the inner tray.

    Product
    Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 47234702116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1366-2016·2016-05-25

    Empirical Labs Recalls Liposomal Magnesium Supplement for Mold Contamination Risk

    Empirical Labs is recalling Liposomal Magnesium Nutritional Supplement due to potential mold contamination. The recall affects 1,972 bottles sold nationwide.

    Product
    Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The product is packaged in a six ounce, plastic, Royalty Bottle, with a 24mm vented flip top lid. item number: DES004Z. Sold under brands DESBIO and Seeking Health
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1669-2016·2016-05-25

    Lumenis M22 IPL Acne Filters Recalled for Superficial Burn Risk

    Lumenis Ltd is recalling M22 IPL Acne Filters due to a risk of superficial burns when using the device.

    Product
    Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-1372-201·2016-05-25

    Nice! Mixed Fruit Recalled for Potential Glass Contamination

    Milky Way Intl Trading Corp is recalling Nice! Mixed Fruit in 8-ounce jars due to potential glass in the product.

    Product
    Mixed Fruit (In Light Syrup), Net Wt. 8oz (227g), Bottle Label UPC 0-49022-80896-6, Case UPC 100-49022-80896-3
    Category
    Food
    Distribution
    Distributed nationwide