Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

10001–10025 of 31231

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 (Devices)·Z-0507-2025·2024-12-04
V.A.C. Ulta Therapy Units Recalled Due to Occlusion Sensor Failures
KCI USA is recalling 83,721 V.A.C. Ulta Negative Pressure Wound Therapy Units due to broken occlusion sensors that may prevent the device from initiating therapy. Affected units are distributed worldwide.
Product
V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an integrated wound management system that provides Negative Pressure Wound Therapy with an instillation option.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0539-2025·2024-12-04
Philips Breast MRI System Recalled for Patient Safety Risk
Philips is recalling 5,231 units of the dS Breast 7ch 1.5T breast MRI system due to a potential safety issue that could harm patients during preparation or scanning.
Product
dS Breast 7ch 1.5T
Category
Medical Device
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-0528-2025·2024-12-04
Smiths Medical Tracheal Tube Exchange Guide Recalled for Inadequate Disinfection Risk
Smiths Medical recalled its PORTEX Tracheal Tube Exchange Guide due to potential fluid ingress during reprocessing that may compromise disinfection standards and pose a contamination risk.
Product
smiths medical PORTEX Tracheal Tube Exchange Guide, 15Ch x 70cm, REF 14-504-68 and REF 14-504-68JP
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0206-2025·2024-12-04
Organic Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling organic griddle waffles sold under multiple brand names due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.
Product
GOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR UPC 085239343029 H-E-B 12/9oz GRDL WFL MINI HSTYLE ORG-HEBUT UPC 041220708413 365 ORGANIC 12/9oz GRDL WFL MINI HSTYLE ORG - 365OR UPC 099482436995 WEGMANS 12/9oz GRDL WFL MINI HSTYLE ORG - WEGMN UPC 077890481448
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0214-2025·2024-12-04
Breakfast Best Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of Breakfast Best griddle waffles for potential Listeria monocytogenes contamination. Consumers should discard the product or return it to the retailer.
Product
BREAKFAST BEST 12/12.3oz GRDL WFL CHOC PEP MOCHA-BKBST UPC 04061463991591
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0563-2025·2024-12-04
Baxter Peritoneal Dialysis Transfer Set Connector Separation Recall
Baxter is recalling 83,448 units of MiniCap Extended Life PD Transfer Sets due to reports of female connector separation from the device body.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0560-2025·2024-12-04
Baxter MiniCap Peritoneal Dialysis Transfer Set Connector Separation Recall
Baxter is recalling 22,392 units of MiniCap Extended Life PD Transfer Sets (Part Number 5C4482EJ) due to reports of female connector separation. Affected units were distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0172-2025·2024-12-04
Krusteaz Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Krusteaz 12-pack griddle waffles 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
KRUSTEAZ 12/9oz GRDL WFL BLBRY MINI-KRSTZ UPC 041820819120
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0207-2025·2024-12-04
Kodiak Cakes Mini Griddle Waffles Recalled for Listeria Contamination Risk
Treehouse Foods recalls Kodiak Cakes 8/9.88oz Mini Griddle Waffles sold nationwide due to 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
KODIAK CAKES 8/9.88oz GRDL WFL ORIG MINI-KDKCS UPC 705599017148
Category
Food
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 (Food)·F-0147-2025·2024-12-04
Hannaford Seafood Salad Recalled for Undeclared Soy Protein Allergen
Hannaford brand seafood salad is recalled because it contains undeclared hydrolyzed soy protein. Consumers with soy allergies should be aware of this risk.
Product
Hannaford brand seafood salad; Net Wt. 12 oz. (340g); INGREDIENTS: SEAFOOD BLEND (FISH PROTEIN [ALASKA POLLOCK AND/OR PACIFIC WHITING], WATER, WHEAT STARCH, SUGAR, SORBITOL, MODIFIED POTATO STARCH, CONTAINS 2% OR LESS OF: NATURAL AND ARTIFICIAL CRAB FLAVORS [SWIMMING CRAB, SNOW C
Category
Food
Distribution
0 states
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 (Devices)·Z-0512-2025·2024-12-04
MEDLINE Procedure Kits: Connectors May Prevent Intended Catheter Insertion
MEDLINE procedure kits are being recalled because connectors may not allow proper catheter insertion if not fully opened. The recall affects 3006 units distributed in the US and internationally.
Product
MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZATION KIT, REF PAIN1644
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0562-2025·2024-12-04
Baxter MiniCap Peritoneal Dialysis Sets Recalled for Connector Separation
Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets due to increasing reports of the female connector separating from the main body. The defect affects 62,718 units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0159-2025·2024-12-04
Treehouse Foods Griddle Pancakes Recalled for Listeria Risk
Treehouse Foods is recalling H-E-B and Trader Joe's griddle pancake products nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 through October 2025.
Product
H-E-B 12/14.1oz GRDL PNCK MINI HSTYLE ORG-HEBUT UPC 041220982714 TRADER JOE'S 16/11.3oz GRDL PNCK MINI HSTYLE ORG-TRDJO UPC 686151803778
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0177-2025·2024-12-04
Griddle waffles recalled for potential Listeria contamination
Treehouse Foods recalls KRUSTEAZ and GOOD & GATHER griddle waffles due to 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
KRUSTEAZ 1/3.44lb GRDL WFL BLGN DBL CHOC-KRSTZ UPC 00041820818734 KRUSTEAZ 12/13.75oz GRDL WFL BLGN DBL CHOC-KRSTZ UPC 041820818697 GOOD & GATHER 12/13.75oz GRDL WFL BLGN DBL CHOC-GDGTR UPC 085239157930
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2025·2024-12-04
Philips dS Breast 16ch 1.5T MRI Recalled for Patient Safety Risk
Philips North America is recalling approximately 5,231 dS Breast 16ch 1.5T MRI systems nationwide due to a potential safety issue that could harm patients during scan preparation or procedures.
Product
dS Breast 16ch 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0169-2025·2024-12-04
Kodiak Cakes Griddle Waffles Recalled Due to Listeria Risk
Treehouse Foods recalls Kodiak Cakes 8/14.8oz Griddle Waffles due to potential Listeria monocytogenes contamination. Affected products carry batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Product
KODIAK CAKES 8/14.8oz GRDL WFL BLGN BLBRY-KDKCS UPC 705599014826
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0195-2025·2024-12-04
Frozen griddle waffles recalled for potential Listeria contamination
Treehouse Foods recalls frozen griddle waffles nationwide due to potential Listeria monocytogenes contamination. Products with batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025 may be affected.
Product
IRRESISTIBLES LIFE SMART 12/240g GRDL WFL HSTYLE GF-IRRLS UPC 059749977661 GOOD & GATHER 12/11.3oz GRDL WFL HSTYLE GF-GDGTR UPC 085239157954 GIANT EAGLE 12/11.3oz GRDL WFL HSTYLE GF-GT/EG UPC 030034944933 PRESIDENT'S CHOICE 12/320g GRDL WFL HSTYLE GF-PCHOI UPC 060383038670 WILD H
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0180-2025·2024-12-04
Krusteaz Griddle Waffles Recalled for Potential Listeria Monocytogenes
Treehouse Foods is recalling Krusteaz brand griddle waffles due to potential Listeria monocytogenes contamination. Products were distributed nationwide in the USA and Canada.
Product
KRUSTEAZ 1/3.44lb GRDL WFL BLGN PMPKNN - KRSTZ UPC 686151805277 KRUSTEAZ 12/13.75oz GRDL WFL BLGN PMPKN-KRSTZ UPC 686151805345
Category
Food
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-0548-2025·2024-12-04
Philips ST SENSE Breast Imaging Coil Recalled for Patient Safety Risk
Philips is recalling 5,231 units of the ST SENSE Breast Dx Coil nationwide due to a potential safety issue that may harm patients during breast imaging scans. No injuries have been reported.
Product
ST SENSE Breast Dx Coil
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0547-2025·2024-12-04
Philips ST SENSE Breast Coil Recalled for Potential Patient Safety Risk
Philips is recalling 5,231 ST SENSE Breast Coils nationwide due to a potential safety issue that could harm patients during MRI scanning. Affected units are identified by specific serial numbers.
Product
ST SENSE Breast Coil
Category
Medical Device
Distribution
Distributed nationwide

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10001–10025 of 31231