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

8126–8150 of 27535

HighFDA (Devices)·Z-1330-2025·2025-03-19
Vista Brite Tip Guiding Catheter Manufactured at Incorrect Length
Cordis US Corp is recalling Vista Brite Tip guiding catheters manufactured at incorrect length. The defect may affect proper catheter placement during interventional or diagnostic vascular procedures.
Product
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-0634-2025·2025-03-19
Ulker Dankek Roll Cake Chocolate recalled due to undeclared egg allergen
Ulker Dankek Roll Cake Chocolate is being recalled because egg is not listed in the Contains statement on the product label. Consumers with egg allergies may be at risk.
Product
Ulker Dankek Roll Cake Chocolate, item 9584, 3oz foil pack, 8 per case, UPC 8690504067979
Category
Food
Distribution
36 states
HighFDA (Devices)·Z-1318-2025·2025-03-19
ZOLL Powerheart G5 AED may fail self-test in extreme environments
ZOLL is recalling certain Powerheart G5 automated external defibrillators (AED) due to the potential for devices to fail their self-test when exposed to extreme temperatures or humidity.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80C, (2) G5A-80C-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1313-2025·2025-03-19
TruScan Body dental scanner recalled due to scanning malfunction
TruAbutment Inc. recalls 61 units of the TruScan Body dental scanner (CN38-SB) due to defects that may prevent proper or accurate scanning.
Product
Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN38-SB Software Version: N/A
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-1322-2025·2025-03-19
ZOLL Powerheart G5 AED Self-Test May Fail Under Extreme Environmental Conditions
ZOLL is recalling certain Powerheart G5 AED units that may fail their self-test when exposed to extreme temperatures or humidity. The affected devices could fail to function properly in emergencies.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9) G5S-80-L (10) G5S-90A; Software Version: NA Product Description: The Powerheart G5 automa
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1311-2025·2025-03-19
Multiple hemostatic forceps models recalled due to clamp breakage risk
Aesculap is recalling 1,147 hemostatic forceps due to clamp breakage risk when used beyond design specifications. Units were distributed nationwide and internationally to healthcare providers.
Product
Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2) REF FB459R, Glover ATR.CLAMP CVD 245MM; (3) REF FB461R, Glover ATR.CLAMP 195MM; (4) REF FB462R, Glover ATR.CLAMP 210MM; (5) REF FB469R, Leland-Jones Peripheral CLMPSTR 195MM;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1298-2025·2025-03-19
GE Revolution CT and Apex systems coolant fluid leak hazard
GE Healthcare Revolution CT and Apex series imaging systems may leak blue coolant fluid near the gantry base, creating a potential slip and fall hazard. Approximately 250 units have been distributed worldwide.
Product
GE Healthcare Revolution Apex Elite, System, X-ray, Tomography, Computed
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1320-2025·2025-03-19
ZOLL Powerheart G5 AED may fail self-test in extreme temperatures or humidity
ZOLL is recalling 73 Powerheart G5 AED units that may fail their internal self-test when exposed to extreme temperatures or humidity. Affected devices could be unreliable in emergencies.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat i
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0264-2025·2025-03-19
Latanoprost medication recalled due to manufacturing practice deviations
Aspen Biopharma Labs is recalling Latanoprost medication due to manufacturing practice deviations. The voluntary recall affects product distributed to distributors in Hong Kong and Florida.
Product
Latanoprost NDC# 82187-1002-1 Container Description: Amber colour bottle
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-1310-2025·2025-03-19
Multiple Aesculap Surgical Forceps Models Recalled for Clamp Breakage
Aesculap Inc is recalling 93,714 hemostatic forceps across 83 models due to clamp breakage that occurs when forceps are used in ways not covered by the design.
Product
Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190MM; (2) REF BH304R, Pean Artery Forceps Straight 140MM; (3) REF BH813R, Artery Forceps Curved 250MM; (4) REF BJ016R, Diss.A.Ligat.Forceps S-Shaped CVD.210MM; (5) REF BJ020R, Ove
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1299-2025·2025-03-19
GE Healthcare CT Systems May Leak Coolant Fluid on Floor
GE Healthcare Revolution CT and Apex series systems can leak coolant fluid onto the floor near the gantry, creating a slip and fall hazard. The blue-colored fluid is non-corrosive and not hot, but poses injury risk if not noticed.
Product
GE Healthcare Revolution Apex Expert, System, X-ray, Tomography, Computed
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1319-2025·2025-03-19
ZOLL Powerheart G5 AED May Fail Self-Test in Extreme Environmental Conditions
ZOLL is recalling certain Powerheart G5 AED models that may fail their self-test function when exposed to extreme temperature or humidity. Affected devices might not function properly in emergencies.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-08C, (5) G5A-10C, (6) G5A-13C, (7) G5A-15C, (8) G5A-22C, (9) G5A-41C, (10) G5A-85C, (11) G5A-90C (12) G5A-80-L; Software Version: NA Product Description: The
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1316-2025·2025-03-19
ZOLL Powerheart G5 AED May Fail Self-Test in Extreme Conditions
The ZOLL Powerheart G5 automated external defibrillator may fail its self-test after prolonged exposure to extreme temperatures or humidity levels. This could prevent proper device functioning in an emergency.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4) G5A-03A, (5) G5A-19A, (6) G5A-80A, (7) G5A-80A-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0610-2025·2025-03-19
Genova Solid White Tuna Recalled for Potential Botulism Contamination
Chicken of the Sea recalls Genova branded solid white tuna nationwide due to improperly secured easy-pull lids that may allow Clostridium botulinum contamination.
Product
Genova branded Solid white Tuna; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 00215,
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1302-2025·2025-03-19
GE Revolution CT Systems Potential Coolant Leak Slip-and-Fall Risk
GE Healthcare Revolution CT systems may leak glycol coolant near the gantry base. While the non-toxic fluid poses no chemical hazard, it creates a slip-and-fall risk if not noticed and cleaned.
Product
GE Healthcare Revolution CT, System, X-ray, Tomography, Computed
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1317-2025·2025-03-19
ZOLL Powerheart G5 AED May Fail Self-Test After Environmental Exposure
ZOLL Powerheart G5 AED devices may fail their self-test if exposed to extreme temperatures or humidity. Approximately 56,981 units are being recalled nationwide and internationally.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80A, (2) G5A-80A-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1325-2025·2025-03-19
Da Vinci 5 surgical console foot pedals recalled for spring failure
Intuitive Surgical has recalled 439 Da Vinci 5 surgical console foot tray pedals due to spring failures that can cause pedals to remain pressed and interfere with normal surgical robot operation.
Product
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software Version: N/A . Refer to HHE for additional details. Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0635-2025·2025-03-19
Ulker Dankek Roll Cake Banana recalled for undeclared wheat allergen
ZB Importing LLC is recalling Ulker Dankek Roll Cake Banana due to wheat allergen not being listed in the product label. Consumers with wheat allergies or celiac disease should not consume this product.
Product
Ulker Dankek Roll Cake Banana, item 9620, 8.3oz foil pack, 8 per case, UPC 8690504067986
Category
Food
Distribution
36 states
HighFDA (Food)·F-0632-2025·2025-03-19
Ulker Dankek Roll Cake Strawberry recalled due to undeclared milk allergen
ZB Importing LLC is recalling Ulker Dankek Roll Cake Strawberry because milk is not declared on the label. Products were distributed in multiple US states and Ontario, Canada.
Product
Ulker Dankek Roll Cake Strawberry , item 8298, 8.3oz foil pack, 8 per case, UPC 8690504066828
Category
Food
Distribution
36 states
HighFDA (Devices)·Z-1312-2025·2025-03-19
Aesculap hemostatic forceps recalled due to clamp breakage
Aesculap is recalling 47,078 surgical forceps designed to control bleeding. The devices' clamps break when used outside design parameters, potentially compromising their effectiveness.
Product
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-CVD190MM; (3) REF BH957R, Schnidt Tonsil Forceps SLT-CVD185MM; (4) REF BH959R, Schnidt Tonsil Forceps CVD 185MM; (5) REF BH961R,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1303-2025·2025-03-19
GE Healthcare CT Scanner Systems Recalled Due to Coolant Leak Risk
GE Healthcare is recalling 21 Revolution CT and Revolution Apex series CT systems due to potential coolant fluid leaks near the gantry base. The leaking fluid poses a slip-and-fall hazard if not cleaned up promptly.
Product
GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1307-2025·2025-03-19
CardiFocus Heartlight X3 Cardiac Catheter Sterile Barrier Damage Recall
CardioFocus is recalling 833 units of CardiFocus Heartlight X3 cardiac catheters due to potential damage to the sterile barrier pouch that could compromise product sterility. Affected units were distributed worldwide.
Product
CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in the setting of an Electrophysiology or Catheterization Laboratory Model: 18-5000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0628-2025·2025-03-19
HEB Spinach Artichoke Dip Recalled for Potential Metal Contamination in Texas
HEB is recalling Spinach Artichoke Dip sold in Texas due to potential metal contamination. Consumers should not consume the affected products.
Product
" Spinach Artichoke Dip (Sold Hot) 1 lb " Spinach Artichoke Dip (Sold Cold) 1 lb " Spinach Artichoke Dip (Sold in Bulk for Customer Self Service)
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0271-2025·2025-03-19
Duloxetine Capsules Recalled for N-Nitroso Impurity Exceeding FDA Limits
Breckenridge Pharmaceutical is recalling 11,125 bottles of Duloxetine 20mg capsules nationwide due to N-nitroso-duloxetine impurity above FDA-recommended limits. The impurity was detected during quality control testing.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0624-2025·2025-03-19
Green Chile Bean Burritos Recalled for Undeclared Milk Allergen
Mi Ranchito Foods is recalling Green Chile Bean Burritos because milk is not listed in the ingredient statement, posing a risk for consumers with milk allergies.
Product
Green Chile Bean Burrito, 15 days refrigerated at 33 45 degrees Fahrenheit. 120 days frozen at or below 32 degrees Fahrenheit. Packaged in cellophane wrapper. Net wt. 10 ounces, UPC #21856 11136. Mi Ranchito Foods, Inc. 606 Central Avenue, Bayard, NM 88023
Category
Food
Distribution
0 states

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8126–8150 of 27535