State

Louisiana product recalls

73,486 recalls have nationwide distribution and so reach Louisiana. 6,959 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,959
Critical: 1,109
Severe: 1,737
Most recent: 2026-10-14

Of the 6,959 recalls naming Louisiana we have scored against our rubric, 1,109 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,737 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,959 recalls whose distribution notice names Louisiana specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23251–23275 of 80445

HighFDA (Devices)·Z-0750-2022·2022-03-23
Hologic Panther Fusion Extraction Reagent-X May Produce False Test Results
Hologic is recalling Panther Fusion Extraction Reagent-X kits due to failed stability specifications that may cause false negative test results. Healthcare providers should stop using affected lots.
Product
Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X Fusion Capture reagent-X 4 EA, FER-X Fusion Enhancer Reagent-X (Lithium Hydroxide Solution) 4 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0769-2022·2022-03-23
JAGTOME RX medical device recalled for sterile barrier breach
Boston Scientific's JAGTOME RX medical device (367 units) is being recalled worldwide due to a sterile barrier breach that compromises device sterility.
Product
JAGTOME RX 39-20-450-025 Material Number: M00573090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2022·2022-03-23
Boston Scientific JAGTOME RX device recalled for sterile barrier breach
Boston Scientific has recalled 2209 units of the JAGTOME RX medical device worldwide due to compromised sterility from a sterile barrier breach. The affected units were distributed across the US and more than 40 countries.
Product
JAGTOME RX 44-30-260-035 Material Number: M00573060
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0807-2022·2022-03-23
BioPlex 2200 Syphilis Calibrator Set Recall Due to Vaccine Interference and Reagent Stability Issues
Bio-Rad Laboratories is recalling 724 BioPlex 2200 Syphilis Calibrator sets due to COVID-19 vaccine interference concerns and manufacturing problems with reagent stability. The recalled lots were distributed nationwide in the U.S. and internationally.
Product
BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0869-2022·2022-03-23
Honey BBQ seasoning recalled due to undeclared wheat allergen
PS Seasoning & Spices recalls Honey BBQ Snack seasoning (3,001 units) distributed to 28 states and Canada due to undeclared wheat. Consumers with wheat allergies should not use affected lots.
Product
Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456. 2. 685-B, Net Wt 5.25 lbs. (2.38kg). Part #020001457. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder…
Category
Food
Distribution
27 states
HighFDA (Food)·F-0879-2022·2022-03-23
Port City Soups Baton Rouge Beans Recalled for Improper Acidification Process
Port City Soups Baton Rouge Beans in 32-oz glass jars are being recalled due to an unapproved production process for acidified foods. The recall affects products sold in Alabama, Louisiana, Mississippi, and Tennessee.
Product
Port City Soups Baton Rouge Beans 32oz glass mason jar sold by individual unit
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0795-2022·2022-03-23
Lumbar Puncture Tray Adult recalled due to manometer failure and leaking
Bard Peripheral Vascular Inc is recalling 8,630 lumbar puncture trays due to manometer failure causing leaking and mating issues. Devices were distributed nationwide in the U.S. plus Puerto Rico, Costa Rica, and Hong Kong.
Product
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0791-2022·2022-03-23
Lumbar Puncture Tray Pediatric Recalled Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling pediatric lumbar puncture trays due to manometer leaking and mating failures that could prevent proper pressure measurement during procedures.
Product
LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0781-2022·2022-03-23
Boston Scientific RX Cholangiogram Kit Recall Due to Sterile Barrier Breach
Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.
Product
RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0766-2022·2022-03-23
Boston Scientific recalls 68 medical devices with sterility breach
Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.
Product
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2022·2022-03-23
HYDRATOME RX surgical device recalled due to sterile barrier breach
Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.
Product
HYDRATOME RX 44-30MM/450CM Material Number: M00583070
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0790-2022·2022-03-23
FDA Recalls Safe-T PLUS Pediatric Lumbar Puncture Tray Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling 20,400 Safe-T PLUS pediatric lumbar puncture trays due to manometer leaking and mating failures. The devices were distributed nationwide and internationally to healthcare facilities.
Product
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2022·2022-03-23
Medical Device Recall: Boston Scientific JAGTOME RX Sterile Barrier Breach
Boston Scientific is recalling 98 units of the JAGTOME RX 39-30-260-025 medical device due to compromised sterile barrier that affects device sterility. Units were distributed worldwide.
Product
JAGTOME RX 39-30-260-025 Material Number: M00573100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2022·2022-03-23
Boston Scientific JAGTOME RX Recalled for Sterile Barrier Breach
Boston Scientific is recalling 96 units of JAGTOME RX medical devices due to a sterile barrier breach that compromises device sterility. Patients should contact their physician if they received this device.
Product
JAGTOME RX 49-30-260-035 Material Number: M00573020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0776-2022·2022-03-23
Medical Device Sterile Barrier Breach: JAGTOME RX Recall
Boston Scientific is recalling JAGTOME RX medical devices because the sterile barrier may be compromised, which could allow contamination. The recall affects 163 units distributed worldwide.
Product
JAGTOME RX 44-30-450-035 Material Number: M00573070
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0788-2022·2022-03-23
LYFO Disk Quality Control Product Recalled for Organism Mislabeling
Microbiologics Inc recalls LYFO Disk lot 983-40-3 because it is labeled as Candida tropicalis but actually contains Yersinia enterocolitica. The mislabeling may cause laboratory quality control failures and delayed test results.
Product
LYFO Disk
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0805-2022·2022-03-23
Calcium Alginate Wound Dressings Recalled for Incorrect Instructions
CellEra LLC is recalling Vitale Silver calcium alginate dressings nationwide because packages contain incorrect Instructions for Use with language not approved by the FDA. The firm is providing replacement packages with corrected instructions.
Product
20548 Vitale Silver calcium Alginate Dressings 4x8, 5/box
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0876-2022·2022-03-23
Port City Soups Tex-Mex Chili Recalled for Unapproved Acidified Food Process
Tony's Tejas Salsa is recalling Port City Soups Tex-Mex Chili because the production process was not approved for acidified foods. The recall affects 81 units distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
Port City Soups Tex-Mex Chili 32oz glass mason jar sold by individual unit
Category
Food
Distribution
4 states
ModerateFDA (Food)·F-0870-2022·2022-03-23
Seasoning Recall: Undeclared Wheat in Honey BBQ Snack Stick Seasoning
PS Seasoning & Spices, Inc. recalled Honey BBQ Snack Stick Seasoning containing undeclared wheat, affecting approximately 10,441 units distributed across multiple U.S. states and Canada. Consumers with wheat allergies should not consume affected products.
Product
Honey BBQ Snack Stick Seasoning packaged in the following sizes: 1. 765-A, Net Wt 21 lbs. (9.52kg). Part #020001203. 2. 765-B, Net Wt 5.25 lbs. (2.38kg). Part #020001299. 3. 765-C, Net Wt 2.63 lbs (1.19kg). Part #020001513. Ingredients: Sugar, Salt, Dried…
Category
Food
Distribution
27 states
ModerateFDA (Food)·F-0872-2022·2022-03-23
FDA Recalls Seasoning Product for Undeclared Wheat Allergen
PS Seasoning & Spices, Inc. recalled Maplewood Meats Honey BBQ Stick Seasoning (lot 2022-53578) for undeclared wheat. The product was distributed across multiple U.S. states and Canada; consumers with wheat allergies should not use it.
Product
Maplewood Meats Honey BBQ Stick Seasoning Net Wt 21 lbs. (9.50kg). Part #180002067. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Monosodium Glutamate, Natural Smoke Flavor, Sodium Erythorbate (0.26%), Dried Molasses, Natural Flavors…
Category
Food
Distribution
27 states
ModerateFDA (Food)·F-0878-2022·2022-03-23
Port City Soups Thai Green Curry recalled for unapproved production process
Tony's Tejas Salsa is recalling Port City Soups Thai Green Curry (32oz glass jars) because the production process has not been approved for acidified foods. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Product
Port City Soups Thai Green Curry 32oz glass mason jar sold by individual unit
Category
Food
Distribution
4 states
ModerateFDA (Drugs)·D-0653-2022·2022-03-23
hydrALAZINE HCl Tablets 10 mg Recalled for Failed Impurity Specifications
The Harvard Drug Group is recalling hydrALAZINE HCl Tablets, USP, 10 mg due to failed impurity and degradation specifications detected during routine stability testing. The recall affects 5,953 cartons distributed nationwide.
Product
hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton (10x10 blister packs), Rx only, Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152 USA. NDC # 0904-6440-61
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0873-2022·2022-03-23
WAP Honey BBQ Seasoning Recalled Due to Undeclared Wheat Allergen
PS Seasoning & Spices, Inc. is recalling WAP Honey BBQ Seasoning because it contains undeclared wheat. Consumers with wheat allergies should not consume this product.
Product
WAP Honey BBQ Seasoning Net Wt 20.64 lbs. (9.36kg). Part #180002073. Ingredients: Raw Cane Sugar, Sea Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder, Dried Molasses, Natural Flavors.
Category
Food
Distribution
27 states
ModerateFDA (Devices)·Z-0802-2022·2022-03-23
Calcium Alginate Wound Dressings Recalled for Incorrect Instructions
CellEra LLC is recalling Vitale Silver calcium alginate wound dressings nationwide due to incorrect instructions for use containing language beyond FDA-cleared content.
Product
20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0804-2022·2022-03-23
Calcium alginate wound dressings recalled for incorrect instruction labeling
CellEra LLC is recalling Vitale Silver calcium alginate dressings because the included Instructions for Use contain language exceeding FDA clearance. The firm is replacing affected units with correct instructions.
Product
20545 Vitale Silver calcium Alginate Dressings 4x5, 10/box
Category
Medical Device
Distribution
Distributed nationwide