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.

50426–50450 of 80793

HighFDA (Devices)·Z-0377-2017·2016-11-16
AtriClip LAA Exclusion System Recalled for Potential Component Failure
AtriCure, Inc. is recalling 298 AtriClip LAA Exclusion Systems due to a potential component failure that could require medical intervention.
Product
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's left atrial appendage, under direct visualization, in conjunction with other open cardiac surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·17033·2016-11-16
Skidders Recalls Children's Shoes Due to Sharp Rivet Laceration Hazard
Skidders Footwear is recalling about 5,500 children's canvas tennis shoes because sharp rivets pose a laceration hazard. Consumers should take shoes away from children and contact the company for a refund.
Product
Children's shoes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0423-2017·2016-11-16
Brownwood Farms Cherry Butter Recalled for Undeclared Milk Allergen
Brownwood Farms is recalling Cherry Butter products because they contain milk that is not declared on the label.
Product
Brownwood Farms America's Original Cherry Butter 12oz and 22oz glass bottles and 1 gallon. Private labels: Arbor Day Farm (Cherry Butter 12oz). Bowers Harbor Vineyards (Cherry Butter 12oz). Crossroads (10oz). Central Market (16oz).
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0420-2017·2016-11-16
Brownwood Farms Cherry Raspberry Preserves Recalled for Undeclared Milk
Brownwood Farms is recalling Cherry Raspberry Preserves because the product contains milk that is not declared on the label.
Product
Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0422-2017·2016-11-16
Brownwood Farms Jalapeno Cherry Butter Recalled for Undeclared Milk
Brownwood Farms is recalling Jalapeno Cherry Butter products because they contain milk that is not declared on the label.
Product
Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Jalapeno Cherry Butter 12oz). Benjamin Twiggs (Cherry Pepper Jam 10oz). Central Market (16oz).
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0392-2017·2016-11-16
Reshape Medical Recalls Integrated Dual Balloon System Due to Fluid Leak Risk
Reshape Medical is recalling 114 units of the Integrated Dual Balloon System Gen 1 because distillation fluid may leak during inflation.
Product
ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape Integrated Dual Balloon System is indicated for weight reduction when used in conjunction with diet and exercise, in obese patients with a Body Mass Index…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0387-2017·2016-11-16
Roche COBAS INTEGRA c111 Analyzer Recall for Software Error
Roche is recalling 139 COBAS INTEGRA c111 analyzers due to a software error that may cause erroneous test results.
Product
Roche COBAS INTEGRA c111 Analyzer, Chemistry (Photometric, Discrete), for clinical use Product Usage: The Roche COBAS INTEGRA c111 analyzer is an in-vitro diagnostic analyzer capable of performing clinical chemistry, specific protein and electrolyte tests. Analytes are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0421-2017·2016-11-16
Brownwood Farms Pear Preserves Recalled for Undeclared Milk Allergen
Brownwood Farms is recalling Pear & Cinnamon Preserves because the product contains milk that is not declared on the label.
Product
Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0425-2017·2016-11-16
Brownwood Farms Cherry Preserves Recalled for Undeclared Milk
Brownwood Farms is recalling Michigan Cherry Preserves because they contain milk that is not declared on the label.
Product
Brownwood Farms Michigan Cherry Preserves 12oz glass bottles and 1 gallon. Private labels: Art's Tavern (Cherry Preserves 12oz).
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V829000·2016-11-16
Mercedes-Benz Recalls S-Class Vehicles for Seat Belt Extender Defect
Mercedes-Benz is recalling 672 S-Class vehicles because seat belt extenders may not retract or may break in a crash, increasing injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG S65, S65 AMG, AMG S63, S550
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0424-2017·2016-11-16
Brownwood Farms Strawberry Preserves Recalled for Undeclared Milk
Brownwood Farms is recalling Strawberry Preserves because the product contains milk that is not declared on the label.
Product
Brownwood Farms Strawberry Preserves 12oz glass bottles and 1 gallon. Private labels: Art's Tavern (Strawberry Preserves 12oz).
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0326-2017·2016-11-16
On the Border Blue Corn Tortilla Chips Recalled for Metal Fragments
Truco Enterprises is recalling On the Border Blue Corn Tortilla Chips due to possible metal fragments in the corn flour.
Product
On the Border Blue Corn Tortilla Chips 7.25 oz. and 10 oz. packaged in laminated polypropylene film with windows.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0394-2017·2016-11-16
Becton Dickinson Recalls Spinal Anesthesia Trays Containing Recalled Lidocaine
Becton Dickinson is recalling specific BD Spinal Anesthesia Trays because they contain Hospira 5% Lidocaine HCI ampules that are subject to a separate recall.
Product
catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 in. BD" Quincke Spinal Needle Lidocaine HCL (5%) with Dextrose (7.5%), 2 mL catalog # 405622 BD Spinal Anesthesia Tray 25G x 3.5 in. BD" Quincke Spinal Needle Bupivacaine HCL (0.75%) with Dextrose (8.25%), 2 mL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0368-2017·2016-11-16
Zimmer Air Dermatome II Handpiece Recalled for Surface Coating Defects
Zimmer Biomet Surgical is recalling Air Dermatome II Handpiece loaners because the surface coating may blister, peel, or discolor over time. No injuries have been reported.
Product
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0366-2017·2016-11-16
FDA Recalls Custom Packaging for Devon Light Gloves
The FDA is recalling custom packaging for Devon Light Gloves due to added instructions for use regarding barrier integrity inspection.
Product
Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove Item Number Description 380789003 SURE SET SINGLE BASIN PACK 400383006 MAJOR BASIN PACK…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0328-2017·2016-11-16
Rich Products Recalls Chocolate Iced Éclairs for Plastic Foreign Material
Rich Products Corp is recalling specific lots of New York Style Chocolate Iced Éclairs due to the potential presence of plastic foreign material.
Product
New York Style Chocolate Iced ¿clairs under the following labels: 1) Richs New York Style Chocolate Iced ¿clairs, NET WT 8 oz (226g) (UPC Code:049800147799), 2) Bakery Fresh Goodness NY Style Chocolate ¿clairs, NET WT 8 oz (226g) (UPC Code:011110456601), 3) Food Lion NY Style…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0365-2017·2016-11-16
FDA Recalls Covidien Devon Light Glove Sub-Assembly for Added Instructions
The FDA is recalling 118,800 units of the Covidien Devon Light Glove sub-assembly to add instructions for use regarding barrier integrity inspection.
Product
Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0379-2017·2016-11-16
Abbott Recalls Architect Lactic Acid Assay Due to Drug Interference
Abbott is recalling 26,837 kits of the ARCHITECT Lactic Acid assay because the drug N-Acetyl Cysteine causes negative interference with the reagent.
Product
ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay is used for the quantitation of lactic acid in human plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0364-2017·2016-11-16
FDA Adds Instructions for Use to Covidien Devon Light Glove Recall
The FDA is adding instructions to inspect the barrier integrity of the Covidien Devon Light Glove after application. This affects sterile surgical kits distributed in the US and abroad.
Product
Covidien Devon Light Glove packaged in sterile surgical kits Reference: 31140208 Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0372-2017·2016-11-16
Schaerer Surgical Table Floor Locking Cylinders Recalled for Leak Risk
Schaerer Medical USA Inc is recalling replacement floor locking cylinders for model 7300 surgical tables because they may leak due to an incorrect O-ring.
Product
Replacement floor locking cylinders for the Schaerer model 7300 surgical tables. Replacement cylinders are part number 85118. Product Usage: The cylinders are used to lock the surgical table in place.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0369-2017·2016-11-16
Medimaps TBS iNsight Software Recalled for Incorrect FRAX Calculations
Medimaps Group is recalling TBS iNsight v.3.0.1 software because FRAX values are incorrect when specific spine scan conditions are met.
Product
TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a medical device software that is installed on bone densitometers for analysis of bone microarchitecture and osteoporosis management.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0371-2017·2016-11-16
Schaerer 7300 Surgical Tables Recalled for Defective Floor Locking Cylinders
Schaerer Medical USA Inc is recalling four 7300 model surgical tables because defective floor locking cylinders may leak due to incorrect O-rings.
Product
The surgical table is a stand alone unit. Three (3) floor locking cylinders are attached to the base of the surgical table. The individual cylinders are replaceable. Product Usage: The cylinders are used to lock the surgical table in place.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0135-2017·2016-11-16
Mylan Recalls Clonazepam Tablets Due to Impurity Specification Failure
Mylan Institutional, Inc. is recalling specific lots of Clonazepam Tablets, USP, 0.5 mg because they failed impurity specifications.
Product
Clonazepam Tablets, USP, 0.5 mg, packaged in a)100- count unit dose box of 10 x 10 blister cards (NDC 51079-881-20) and b) 300-count unit dose box of 10 x 30 punch cards (NDC 51079-881-56), Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0136-2017·2016-11-16
Mylan Recalls Clonazepam Tablets Due to Impurity Specification Failure
Mylan Institutional is recalling specific lots of Clonazepam 1.0 mg tablets because a known impurity exceeded specification limits during stability testing.
Product
Clonazepam Tablets, USP, 1.0 mg, packaged in a 100- count unit dose box of 10 x 10 blister cards, Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505, NDC 51079-882-20
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0134-2017·2016-11-16
Taro Recalls Kamedis Dandruff Care Kits Due to Low Active Ingredient
Taro Pharmaceuticals is recalling 17,100 kits of Kamedis Bio-Herbal Dandruff Care System because the active ingredient, zinc pyrithione, was found to be subpotent.
Product
Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM - Kamedis Bio-Herbal Dandruff Care 0.1% PYRITHIONE ZINC, STEP 1 PRE-TREAT Concentrated Botanical Scalp Lotion (0.1% Pyrithione Zinc) 4.20 FL OZ (125mL) (NDC 51672-2126-0) and STEP 2 CLEANSE Concentrated…
Category
Drug
Distribution
Distributed nationwide