State

Mississippi product recalls

73,092 recalls have nationwide distribution and so reach Mississippi. 5,377 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total: 5,377
Critical: 933
Severe: 1,138
Most recent: 2026-09-23

Of the 5,377 recalls naming Mississippi we have scored against our rubric, 933 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,138 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,377 recalls whose distribution notice names Mississippi specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9001–9025 of 78469

HighFDA (Food)·F-0170-2025·2024-12-04
Multiple Store-Brand Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of frozen griddle waffles with blueberries distributed nationwide in the USA and Canada due to potential Listeria monocytogenes contamination.
Product
PRESIDENT'S CHOICE 12/320g GRDL WFL BLBRY GF-PCHOI UPC 060383038663 WILD HARVEST 12/11.3oz GRDL WFL BLBRY GF-WLDHR UPC 711535515173 WEGMANS 12/11.3oz GRDL WFL BLBRY GF-WEGMN UPC 077890519653 FULL CIRCLE 12/11.3oz GRDL WFL BLBRY GF-FULLC UPC 036800486980 FOODHOLD 12/11.3oz GRDL WF
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0518-2025·2024-12-04
GE SIGNA Architect MRI Systems Recalled for Elevated Acoustic Noise
GE Medical Systems is recalling certain SIGNA Architect MRI systems because their gradient coils can produce elevated acoustic noise during scanning under specific conditions, potentially risking hearing damage.
Product
SIGNA Architect, Nuclear Magnetic Resonance Imaging System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0535-2025·2024-12-04
VITROS Chemistry CRP Diagnostic Slides May Underreport Elevated Results
Ortho-Clinical Diagnostics is recalling 7,717 units of VITROS CRP diagnostic slides that may produce falsely low results for high C-reactive protein samples, risking missed diagnosis of infection or inflammation.
Product
VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP) concentration in serum and plasma Model/Catalog Number: 1926740
Category
Medical Device
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-0553-2025·2024-12-04
Shimadzu Autosampler Water Intrusion May Cause Electrical Short Circuit
Shimadzu laboratory autosamplers are being recalled due to water intrusion from a dehumidifier that can cause electrical short circuits. Affected units are distributed worldwide, including across the United States.
Product
Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0514-2025·2024-12-04
MEDLINE Neuraxial Kit Connectors May Prevent Catheter Insertion
MEDLINE has recalled 360 units of its Neuraxial Kit (Lot 23KLA330) because connectors may not fully open, potentially preventing catheters from being inserted as intended. Healthcare facilities should discontinue use and contact MEDLINE.
Product
MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0544-2025·2024-12-04
Philips Mammotrak Interventional Coil MRI Device Recalled for Patient Safety
Philips recalls 5,231 Mammotrak Interventional Coil 3.0T MRI devices nationwide due to a potential safety issue that could harm patients during scan preparation or imaging.
Product
Mammotrak Interventional Coil 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0197-2025·2024-12-04
Organic Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of organic griddle waffles from multiple brands due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Product
WEGMANS 12/7.4oz GRDL WFL HSTYLE ORG - WEGMN UPC 077890481400 NATURE'S BASKET 12/7.41oz GRDL WFL HSTYLE ORG-NTBKU UPC 030034944483 NATURE'S PROMISE 12/7.4oz GRDL WFL HSTYLE ORG - NTRPR UPC 688267058431 O ORGANICS 12/7.4oz GRDL WFL HSTYLE ORG-OORGN UPC 079893801155 SIMPLE TRUTH OR
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
HighFDA (Food)·F-0194-2025·2024-12-04
Griddle waffle and pancake mixes recalled due to Listeria monocytogenes
Treehouse Foods is recalling multiple brands of griddle waffle and pancake mixes nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 1, 2024, to October 11, 2025.
Product
NO NAME 1/1.68kg GRDL WFL HSTYLE - NNAME UPC 060383987756 WESTERN FAMILY 12/280g GRDL WFL HSTYLE - WSTCN UPC 062639310165 GREAT VALUE 12/280g GRDL WFL HSTYLE - GRVLC UPC 681131712934 NO NAME 12/280g GRDL WFL HSTYLE - NNAME UPC 060383987664 YELLOH 12/19.75oz GRDL WFL HSTYLE-YLLOH
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0162-2025·2024-12-04
H-E-B and Central Market Griddle Waffles Recalled for Listeria Risk
H-E-B and Central Market brand griddle waffles with apple cinnamon are being recalled nationwide due to potential Listeria monocytogenes contamination affecting 9,907,389 cases.
Product
H-E-B 12/9oz GRDL WFL APL CIN ORG-HEBUT UPC 041220708376 CENTRAL MARKET 12/9oz GRDL WFL APL CIN ORG - CTMKT UPC 041220655748
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0200-2025·2024-12-04
Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of Krusteaz griddle waffles and related products due to potential Listeria monocytogenes contamination. Products with batch codes starting with 2C and best-by dates through October 11, 2025 are included.
Product
KRUSTEAZ 1/2.5lb GRDL WFL BLGN 7-KRSTZ UPC 068615115168 KRUSTEAZ 1/11.25oz GRDL WFL BLGN-KRSTZ UPC BAKERS SOURCE 1/11.25oz GRDL WFL BLGN-BKRSC UPC 089356143562 GORDON FOOD SERVICE 3/2.5lb GRDL WFL BLGN 7-GDNFS UPC 093901310323
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0166-2025·2024-12-04
Nature's Path Organic Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Nature's Path Organic Griddle Waffles (9,907,389 cases) for potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.
Product
NATURES PATH ORGANIC 12/7.4oz GRDL WFL BCKWHE BRY ORG GF-NPTHO UPC 058449590583 NATURES PATH ORGANIC 12/210g GRDL WFL BCKWHE BRY ORG GF-NPOCN UPC 058449590576
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0536-2025·2024-12-04
Philips Achieva TX Interventional Coil 3.0T Recalled for Patient Safety Risk
Philips recalls the Achieva TX Interventional Coil 3.0T (5,231 units) for a potential safety issue that may harm patients during MRI scan preparation or procedures.
Product
Achieva TX Interventional Coil 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0538-2025·2024-12-04
Philips dS Breast MRI System Recalled for Patient Safety Hazard
Philips dS Breast 16ch 3.0T MRI systems are being recalled due to a potential safety issue that could harm patients during medical scans. The FDA-mandated Class II recall affects 5,231 units distributed nationwide.
Product
dS Breast 16ch 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0542-2025·2024-12-04
Mammotrak Interventional Coil 1.5T recalled for patient safety risk
Philips is recalling 5,231 units of the Mammotrak Interventional Coil 1.5T nationwide due to a potential safety issue that may harm patients during MRI preparation or scanning.
Product
Mammotrak Interventional Coil 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0513-2025·2024-12-04
MEDLINE Epidural and Spinal Procedure Kits: Connector May Prevent Catheter Insertion
MEDLINE is recalling 3,744 epidural and spinal procedure kits due to a connector defect that may prevent proper catheter insertion. Affected kits were distributed nationwide and internationally.
Product
MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL W/TUOHY, REF PAIN9023; 4) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1281 5) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN9024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0189-2025·2024-12-04
Kodiak Cakes Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Kodiak Cakes 8/10.72oz Griddle Waffles with Chocolate Chip due to potential Listeria monocytogenes contamination. The recall affects approximately 9,907,389 cases distributed nationwide in the United States and Canada.
Product
KODIAK CAKES 8/10.72oz GRDL WFL CHOC CHIP-KDKCS UPC 705599013201
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0508-2025·2024-12-04
Medline Nexus Catheter Connectors May Fail to Open Properly
Medline recalls 1,975 NEXUS catheter connectors that may not fully open, preventing proper catheter insertion. Affected units were distributed nationwide and internationally.
Product
MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0510-2025·2024-12-04
Medline Epidural Catheter Kits Recalled Due to Connector Position Defect
Medline is recalling over 5,900 epidural catheter kits because the connectors may not open fully, preventing proper catheter insertion. The recall affects units distributed nationwide and internationally.
Product
MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0541-2025·2024-12-04
Mammotrak Diagnostic Coil 1.5T Recalled Due to Patient Safety Concern
Philips is recalling 5,231 Mammotrak Diagnostic Coil 1.5T units nationwide because of a potential patient safety issue during MRI scans. The FDA has classified this as a Class II recall.
Product
Mammotrak Diagnostic Coil 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0063-2025·2024-12-04
Drug recall: Absorbine Jr. Ultra Strength Pain Patch manufacturing deviations
Absorbine Jr. Ultra Strength Pain Patch is being recalled nationwide due to manufacturing process deviations. The voluntary recall affects approximately 4,968,000 patches.
Product
ABSORBINE jr ULTRA STRENGTH PAIN PATCH, Menthol 6.5%, 1 patch per box, Distributed By: Absorbine Jr. LLC, Chattanooga, TN 37402 UPC 8 89476 41318 3, UPC 8 89476 41336 7
Category
Drug
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 (Devices)·Z-0540-2025·2024-12-04
Philips dS Breast 7ch 3.0T MRI Coil Recalled for Patient Safety Hazard
Philips is recalling 5,231 dS Breast 7ch 3.0T breast MRI coils distributed nationwide due to a potential safety issue that may harm patients during scan preparation or scanning. The FDA classified this as Class II.
Product
dS Breast 7ch 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2025·2024-12-04
Medline Surgical Kits Recalled for Incorrect Needle and Suture Specifications
Medline Industries is recalling 408 surgical kits from Alabama, Georgia, Massachusetts, New Jersey, and Pennsylvania. Some suture packages within the kits contain incorrect needle types and sizes, and incorrect suture diameters and lengths.
Product
(1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, non-sterile.
Category
Medical Device
Distribution
Distributed nationwide