State

Louisiana product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46001–46025 of 80783

CriticalFDA (Devices)·Z-2740-2017·2017-07-26
Flowonix Recalls Prometra II Pump After Reported Fatal Overdose During MRI
Flowonix Medical is recalling Prometra II implantable infusion pumps after a report of a fatal drug overdose during an MRI procedure.
Product
PROMETRA II Programmable Infusion Pump, Implantable Infusion Pump, Catalog Number/REF 13827, Part Number PL-31790-02. Manufactured by: Flowonix Medical Inc., --- The correction involves the labeling of the device plus the following Prometra II pump labeling is also being…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2702-2017·2017-07-26
Penumbra 3D Revascularization Device Recalled Due to Delivery Wire Breakage Risk
Penumbra Inc. is recalling 155 units of the 3D Revascularization Device because a raw material issue could cause the delivery wire to break, potentially leading to serious injury or death.
Product
Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral-M1 and M2 segments) within 8 hours of symptom…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2819-2017·2017-07-26
Aldi Millville Granola Recalled for Listeria Contamination Risk
New England Natural Bakers is recalling Aldi Millville Fruit & Nut Whole Grain Granola due to potential Listeria monocytogenes contamination.
Product
Millville Fruit & Nut Whole Grain Granola - 16 oz .carton Distributed by Aldi Inc. Batavia, IL 60510 UPC:041498205232
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2817-2017·2017-07-26
Evoke Organic Muesli Recalled Due to Listeria Contamination Risk
New England Natural Bakers is recalling Evoke Organic Muesli Classic Swiss 12 oz. pouches due to potential Listeria monocytogenes contamination.
Product
Evoke Organic Muesli Classic Swiss 12 oz. pouch UPC: 853305003081
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0991-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection, 7 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5284 NDC# 61553-284-48
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0990-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection, 40 mMol in 250 mL in 250 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5301 NDC# 61553-301-11
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V474000·2017-07-26
Mazda Recalls Vehicles for Air Bag Inflator Rupture Risk
Mazda is recalling specific 2003-2008 models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Product
MAZDA — MAZDA RX-8, MAZDA6, MAZDASPEED6
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2751-2017·2017-07-26
BD 3ml Syringes Recalled for Insufficient Sterilization Irradiation
Becton Dickinson is recalling 648,000 units of BD 3ml Syringes because several lots did not receive the specified dose of irradiation required to meet the Sterility Assurance Level.
Product
BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0995-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 5% Dextrose Injection, 9 mMol in 50 mL in 50 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5310 NDC# 61553-310-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0997-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection because a media fill failure at the manufacturer raised concerns about sterility.
Product
Potassium PHOSphate in 5% Dextrose Injection, 15 mMol in 250 mL in 250 mL Intravia Bag Service, Rx Only. PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5300 NDC# 61553-300-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0986-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection, 10 mMol in a) 100 mL in 150 mL Intravia Bag (NDC 61553-288-48) Service Code: 2K5288, and b) 250 mL in 250 mL Intravia Bag (NDC 61553-281-11) Service Code: 2K5281, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2752-2017·2017-07-26
BD 10mL Syringes Recalled for Insufficient Sterilization Irradiation
Becton Dickinson is recalling 547,600 units of BD 10mL Syringes because several lots did not receive the specified dose of irradiation required to meet Sterility Assurance Level standards.
Product
BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0989-2017·2017-07-26
PharMedium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMedium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 5% Dextrose Injection, 30 mMol 500 mL in 500 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5283 NDC# 61553-283-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0994-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection, 9 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5286 NDC# 61553-286-48
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0992-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection because of a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection, 7.5 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5298 NDC# 61553-298-48NDC# 61553-298-48
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0996-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride Injection due to a media fill failure at the manufacturer that raises concerns about sterility.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection, 30 mMol in a) 250 mL in 250 mL Intravia Bag Service Code 2K5290 NDC# 61553-290-11, b) 500 mL in 500 mL Intravia Bag Service Code 2K5285 NDC# 61553-285-03, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2818-2017·2017-07-26
Evoke Organic Muesli Recalled Due to Listeria Contamination Risk
New England Natural Bakers is recalling Evoke Organic Muesli Athlete Fuel pouches due to potential Listeria monocytogenes contamination.
Product
Evoke Organic Muesli Athlete Fuel -12 oz .pouch UPC: 853305003029
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0985-2017·2017-07-26
PharMedium Recalls Succinylcholine Chloride Injection Due to Sterility Concerns
PharMedium Services is recalling specific lots of Succinylcholine Chloride Injection due to a media fill failure that compromised sterility assurance.
Product
Succinylcholine Chloride Injection (Preserved) 20 mg per mL, 200 mg per 10 mL, 10 mL Total Volume in BD Syringe, For IV Use, PharMedium Services, LLC, Cleveland, MS --- NDC 61553-364-65
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0988-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate Injection due to a media fill failure that raises concerns about sterility.
Product
Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5287 NDC# 61553-287-48
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2816-2017·2017-07-26
New England Natural Bakers Organic Muesli Recalled for Listeria Risk
New England Natural Bakers is recalling Organic Muesli due to potential Listeria monocytogenes contamination. Consumers should check their pantry for the affected product.
Product
New England Natural Bakers Organic Muesli -5lb and 25 lb. cases UPC: 00046689225013
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0993-2017·2017-07-26
PharMEDium Recalls Potassium Phosphate Injection Due to Sterility Concerns
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
Product
Potassium PHOSphate in 5% Dextrose Injection, 7.5 mMol in 100 mL in 150 mL Intravia Bag, Rx Only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478 800-523-7749 Service Code 2K5299 NDC# 61553-299-48
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-3108-2017·2017-07-26
Newly Weds Foods Recalls Breader X1 for Undeclared Milk
Newly Weds Foods is recalling Breader X1 products because they may contain undeclared milk. The affected product was distributed nationwide, in Mexico, and in Canada.
Product
A92337, BREADER X1*, NET WT 25 LBS, Manufactured By: Newly Weds Foods, Inc., Chicago, IL 60639
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-3114-2017·2017-07-26
Newly Weds Foods Recalls Predust X1 for Undeclared Milk
Newly Weds Foods is recalling 4,700 lbs of Predust X1 because the product may contain undeclared milk. The product was distributed nationwide, in Mexico, and in Canada.
Product
A95460, PREDUST X1, NET WT 50 LBS, Manufactured By: Newly Weds Foods, Inc., Chicago, IL 60639
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-3331-2017·2017-07-26
Newly Weds Foods Recalls Breader X1 for Undeclared Milk
Newly Weds Foods is recalling Breader X1 because it may contain undeclared milk. The product was distributed nationwide and to Canada and Mexico.
Product
B94979, BREADER X1, NET WT 50 LBS, Manufactured By: Newly Weds Foods, Inc., Chicago, IL 60639
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-3147-2017·2017-07-26
Newly Weds Foods Recalls Crackers Due to Undeclared Milk
Newly Weds Foods is recalling 40,000 lbs of crackers because they may contain undeclared milk. The product was distributed nationwide, in Mexico, and Canada.
Product
B10337, CRACKER ML X1, NET WT 50 LBS, Manufactured By: Newly Weds Foods, Inc., Chicago, IL 60639
Category
Food
Distribution
Distributed nationwide