State

Louisiana product recalls

72,992 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total: 6,922
Critical: 1,094
Severe: 1,483
Most recent: 2026-09-09

Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9026–9050 of 79914

HighFDA (Food)·F-0179-2025·2024-12-04
Frozen Griddle and Belgian Waffle Products Recalled for Listeria Contamination Risk
Treehouse Foods is recalling multiple frozen griddle and Belgian waffle brands nationwide due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC 091479060275 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151903331 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG-KRSMX UPC 00686151805307 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151904017 GORDON CHOICE 1/3.12kg G
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0156-2025·2024-12-04
Treehouse Foods Griddle Pancakes Recalled for Potential Listeria Contamination
SE Grocers and Pics by Price Chopper brand griddle pancakes are being recalled by Treehouse Foods due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.
Product
SE GROCERS 12/16.5oz GRDL PNCK HSTYLE-SEGGR UPC 038259117194 PICS BY PRICE CHOPPER 12/16.5oz GRDL PNCK HSTYLE-PRCHP UPC 041735157386
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0545-2025·2024-12-04
Philips SENSE Breast Coil Recall for Potential Patient Safety Hazard
Philips is recalling 5,231 SENSE Breast Coils due to a potential patient safety hazard during scan preparation and performance. The FDA has not disclosed specific details about the nature of the risk.
Product
SENSE Breast Coil
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2025·2024-12-04
Discovery MR750w MRI Scanner Recalled for Elevated Acoustic Noise
GE Medical Systems is recalling 8 Discovery MR750w 3.0T MRI scanners because their gradient coils can produce elevated acoustic noise during scanning under specific conditions.
Product
Discovery MR750w 3.0T, whole body magnetic resonance scanner
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0184-2025·2024-12-04
Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of Kodiak Cakes griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates between October 1, 2024 and October 11, 2025.
Product
KODIAK CAKES 8/13.40oz GRDL WFL BTRMLK VAN-KDKCS UPC 705599012211
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0192-2025·2024-12-04
Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Kodiak Cakes griddle waffles due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C with best by dates from October 1, 2024 to October 11, 2025.
Product
KODIAK CAKES 8/10.72oz GRDL WFL DRKCH REFORM-KDKCS UPC 705599012709
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2025·2024-12-04
AMS Artificial Urinary Sphincter Control Pump: Mislabeled Packaging Recall
Boston Scientific recalled 16 units of AMS Artificial Urinary Sphincter Control Pumps due to mislabeled packaging where devices labeled as Pressure Regulating Balloons actually contained Control Pumps.
Product
AMS Artificial Urinary Sphincter Control Pump
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0210-2025·2024-12-04
Trader Joe's Griddle Waffles Pumpkin Recalled for Listeria Contamination Risk
Treehouse Foods is recalling Trader Joe's Griddle Waffles Pumpkin due to potential Listeria contamination. About 9.9 million cases with batch codes starting with 2C and best-by dates October 1 through October 11, 2025, are affected.
Product
TRADER JOE'S 24/9.9oz GRDL WFL PMPKN - TRDJO UPC 000000517263
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0196-2025·2024-12-04
Simple Truth Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Simple Truth griddle waffles with batch codes starting with 2C due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases were distributed nationwide in the USA and Canada.
Product
SIMPLE TRUTH 12/11.3oz GRDL WFL HSTYLE GF-SMPTR UPC 011110105493
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0202-2025·2024-12-04
Griddle waffles recalled due to potential Listeria contamination
Treehouse Foods is recalling multiple store-brand griddle waffles due to potential Listeria monocytogenes contamination. Products were distributed nationwide across the USA and Canada.
Product
WEGMANS 12/7.4oz GRDL WFL MGRN ORG - WEGMN UPC 077890481431 GREENWISE 12/7.4oz GRDL WFL MGRN ORG - GRNWS UPC 041415209541 SE GROCERS NATURALLY BETTER 12/7.4oz GRDL WFL MGRN ORG - SEGNB UPC 607880200867 NATURE'S PROMISE 12/7.4oz GRDL WFL MLTGRN ORG-NTRPR UPC 688267188497 365 ORGAN
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0211-2025·2024-12-04
Nature's Path Organic Griddle Waffles Recalled for Listeria Contamination Risk
Nature's Path Organic 12-pack griddle waffles with batch codes starting 2C and best-by dates between October 2024 and October 2025 are recalled due to potential Listeria monocytogenes contamination. No illnesses reported.
Product
NATURES PATH ORGANIC 12/210g GRDL WFL PMPKN ORG GF-NPTHO UPC 058449590774
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0178-2025·2024-12-04
Treehouse Foods Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling certain griddle waffle products due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.
Product
COMPLIMENTS 12/390g GRDL WFL BLGN MXD BRY-CMPLM UPC 055742347180 CULINARY TOURS 12/13.75oz GRDL WFL BLGN MXD BRY - CLNTR UPC 011225148569
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0069-2025·2024-12-04
LILAS Feminine Pain Relief Patch recalled for manufacturing violations
Unexo Life Sciences is voluntarily recalling LILAS Feminine Pain Relief Patch nationwide due to manufacturing practice deviations affecting 363,300 patches.
Product
LILAS Feminine Pain Relief Patch, Menthol 10%, a) 5 patches per box (UPC 7 87099 48212 1) and 10 patches per box (UPC 7 87099 48211 4), Distributed by: Lilas Wellness, Inc., Beaverton, Oregon 97008-7105
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0551-2025·2024-12-04
Abbott Merlin@home Cardiac Monitoring Transmitters Fail to Update After Power Loss
Abbott is recalling 130 Merlin@home cardiac transmitters that cannot update software after power interruption during firmware download. Affected devices remain on outdated firmware with no ability to receive future updates.
Product
Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted heart device to Merlin.net" Patient Care Network (PCN) to facilitate remote monitoring by using inductive (EX1100 Model) or RF telemetry (E
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2025·2024-12-04
Absorbine Jr Pain Relieving Knee Patch recalled for manufacturing deviations
Unexo Life Sciences is recalling Absorbine Jr Pain Relieving Knee Patch nationwide due to manufacturing process deviations that do not meet FDA standards. No illnesses or injuries have been reported.
Product
ABSORBINE JR PAIN RELIEVING KNEE PATCH, Camphor 7%, Menthol 7%, packaged in a) 1 patch (UPC 8 89476 41251 3) and b) 6 patches (UPC 8 89476 41306 0), Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0558-2025·2024-12-04
Medline Endo Kit Recall: Missing Lot and Expiration Date Labels
Medline is recalling Endo Kit models containing Olympus components with missing sterile and manufacturing lot numbers and expiration dates on packaging. Without this labeling, medical facilities cannot verify product expiration or track inventory.
Product
ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0075-2025·2024-12-04
Menthol pain relief patches recalled for manufacturing practice violations
J.R. Watkins is recalling Cooling Menthol Extra Strength Pain Relief Patches nationwide due to manufacturing practice deviations. The recall affects approximately 7,138 patches from lots JC101, JC102, and JC103.
Product
Cooling Menthol Extra Strength Pain Relief Patch, Menthol 7.5%, packaged in box of 5, Distributed by J.R. Watkins LLC, Oakland CA 94612 UPC 8 56294 00878 5, NDC 72342-100-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0523-2025·2024-12-04
Z-800WF Infusion Pumps Recalled for Software Incompatibility Issue
Zyno Medical LLC is recalling Z-800WF infusion pumps due to incompatibility between WiFi software and the pump's operating software. The affected units were distributed in eight U.S. states.
Product
Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog Number: Z-800WF. The Z-800 Infusion system is intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient under the direction or supervision physician or other certi
Category
Medical Device
Distribution
8 states
ModerateFDA (Drugs)·D-0062-2025·2024-12-04
Topical menthol back patch recalled for manufacturing deviations
ABSORBINE jr. Extra Large Back Patch containing 5% menthol is being recalled nationwide due to manufacturing compliance deviations. The Class II recall affects 6,848,820 patches distributed by Absorbine Jr., LLC.
Product
ABSORBINE jr. Extra Large BACK PATCH, Menthol 5%, 1 extra large patch per box, Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402 UPC 8 89476 41218 6, UPC 8 89476 41236 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2025·2024-12-04
Equate Maximum Strength Lidocaine Pain Relieving Patches Recalled for Manufacturing Deviations
Equate Maximum Strength Lidocaine Pain Relieving Patches (4%) are being recalled due to current Good Manufacturing Practice deviations. Approximately 1.1 million patches were distributed nationwide in the US.
Product
EQUATE PAIN RELIEVING PATCHES — EQUATE PAIN RELIEVING PATCHES (LIDOCAINE 4%)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0072-2025·2024-12-04
Parche Leon pain relief patches recalled for manufacturing deviations
Unexo Life Sciences Private Limited is voluntarily recalling Parche Leon pain relief patches due to manufacturing practice deviations. No illnesses or injuries have been reported.
Product
PARCHE LEON — PARCHE LEON (CAPSAICIN, CAMPHOR, MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0067-2025·2024-12-04
Menthol Patch Recall Due to Manufacturing Quality Deviations
HealthWise Menstrual Pain Relief Patch (Menthol 10%) is recalled due to manufacturing quality deviations. The firm-initiated recall affects 10,368 patches distributed nationwide in the US.
Product
HEALTHWISE MENSTRUAL PAIN RELIEF PATCH — HEALTHWISE MENSTRUAL PAIN RELIEF PATCH (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0520-2025·2024-12-04
GE SIGNA and DISCOVERY PET/MR Scanners Recalled for Elevated Acoustic Noise
GE Medical Systems is recalling SIGNA PET/MR and DISCOVERY PET/MR imaging systems because gradient coils can produce elevated acoustic noise during scanning under specific conditions.
Product
Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance: 1) SIGNA PET/MR, 2) DISCOVERY PET/MR,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0066-2025·2024-12-04
FDA Recalls Menthol Medicated Patches Due to Manufacturing Deviations
FDA recalls THERA CARE COLD HOT MEDICATED PATCH (menthol 5%) due to manufacturing practice deviations. The voluntary recall affects 279,936 patches distributed nationwide.
Product
THERA CARE COLD HOT MEDICATED PATCH — THERA CARE COLD HOT MEDICATED PATCH (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0554-2025·2024-12-04
Shimadzu Autosampler Devices Subject to Water Damage Affecting Main Board
Water condensation may accumulate under the autosampler's thermal insulation and damage the main board, causing communication errors and delays in laboratory testing. Two Shimadzu models are affected: SIL-40C XR CL and SIL-40C X3 CL.
Product
Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
Category
Medical Device
Distribution
Distributed nationwide