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

11401–11425 of 31362

SevereFDA (Devices)·Z-2942-2024·2024-09-11
Trilogy Evo EV300 Ventilator Mandatory Software Update for Safety Issues
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo EV300 ventilators to resolve previously identified safety issues. Approximately 90,910 US units and 56,273 international units are affected.
Product
Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy Evo, O2, Brazil EV300; CA2200X12B Trilogy Evo, O2, Canada EV300; DE2200X13B Trilogy Evo, O2, Germany EV300; DS2200X11B Trilogy Evo, O2, USA EV300; DS2200X11B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2944-2024·2024-09-11
Philips Respironics Trilogy Evo Ventilator Software Update Addresses Safety Issues
Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo ventilators worldwide to resolve identified safety issues. Users must apply the update and review the updated User Manual.
Product
Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18B Trilogy Evo, Brazil CA2110X12B Trilogy Evo, Canada DE2100X13B Trilogy Evo O2, Germany DE2110X13B Trilogy Evo, Germany DS2100X11B Trilogy Evo, O2, US
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1781-2024·2024-09-11
Popsicle Jolly Rancher Frozen Pops Recalled for Undeclared Milk Allergen
Unilever North America is recalling Popsicle Jolly Rancher Frozen Confection Pops nationwide due to undeclared milk, which poses a risk to consumers with milk allergies.
Product
Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL OZ (80 ML). Green Apple Blue Raspberry and Grape flavored. GTIN/UPC 10077567003727 Case UPC 77567003720
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1759-2024·2024-09-11
Butternut Squash Cubes Recalled Due to Listeria Contamination Risk
Butternut squash cubes sold in Kentucky, Michigan, Ohio, and West Virginia are recalled due to potential Listeria monocytogenes contamination. Affected products have sell-by dates between July 9 and July 26, 2024.
Product
Butternut Squash Cubes - 12oz Plastic Clam-Shell Container
Category
Food
Distribution
4 states
SevereFDA (Food)·F-1764-2024·2024-09-11
Guacamole products recalled due to Listeria monocytogenes contamination
JFE Franchising is recalling guacamole products due to Listeria monocytogenes contamination. Affected items were distributed in Kentucky, Michigan, Ohio, and West Virginia with sell-by dates from July 9 to July 26, 2024.
Product
Guacamole & Pico de Gallo Combo $7.99 - 16 oz 639123880574 Guacamole Chunky Medium - 14 oz 639123880161 Guacamole Chunky Mild - 14 oz 639123880154 Guacamole Blender Mild $5.99 - 12 oz 639123880789 Plastic Clam-Shell Container
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-2690-2024·2024-09-11
Vivo 45 LS Ventilator Recall: Potential Formaldehyde Emission Risk
Breas Medical is recalling the Vivo 45 LS ventilator due to potential elevated formaldehyde emissions into the patient breathing airpath under specific conditions.
Product
Vivo 45 LS, pressure and volume ventilator capable of delivering continuous or intermittent ventilatory support for patients who require invasive or non-invasive mechanical ventilation, Model/Catalog Number: 230000 (230016, 230216)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1761-2024·2024-09-11
JFE Franchising salsa medium and mild recalled for Listeria monocytogenes
JFE Franchising is recalling medium and mild salsa products sold in Kentucky, Michigan, Ohio, and West Virginia due to potential Listeria monocytogenes contamination.
Product
Salsa Medium - 16 oz Salsa Mild - 16 oz Plastic Clam-Shell Container
Category
Food
Distribution
4 states
SevereFDA (Food)·F-1763-2024·2024-09-11
Diced Pepper and Fajita Mix Products Recalled for Listeria Contamination
JFE FRANCHISING INC is recalling diced pepper and fajita mix products sold in Kentucky, Michigan, Ohio, and West Virginia due to potential Listeria monocytogenes contamination. Consumers should discard the products or return them to the store.
Product
Diced Pepper Tri-Blend - 8 oz 639123880024 Diced Pepper w/ White Onion - 7 oz 639123880048 Fajita Mix, Hot $5.00 - 11 oz 639123880406 Fajita Mix, Mild $5.00 - 11 oz 639123880390 Diced Jalapeno - 7oz 639123880031 Plastic Clam-Shell Container
Category
Food
Distribution
4 states
HighNHTSA·23V784000·2024-09-11
2024 Big Tex Trailers Recalled for Defective Goodride Tires
Big Tex Trailer Manufacturing is recalling certain 2024 trailers equipped with defective Goodride ST 200 tires. The tire sidewalls may bubble and separate, causing pressure loss and increasing crash risk.
Product
BIG TEX — 2024 BIG TEX 12SR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2952-2024·2024-09-11
Desflurane anesthesia vaporizer recalled for possible excessive anesthetic output
Mindray's Desflurane E_Vap vaporizer may deliver anesthetic at higher concentrations than set due to an incomplete seal. Patients could inhale excessive anesthetic, potentially causing dizziness, drowsiness, and in severe cases, neurological effects.
Product
Desflurane E_Vap.(Saf-T-Fill) used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number: Part Number115-066759-00
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1546-2024·2024-09-11
Beckman Coulter DxI 9000 Analyzer Recalled for Leaking Wash Buffer Tank
Beckman Coulter is recalling 17 DxI 9000 Access Immunoassay Analyzers due to cracks in the Internal Wash Buffer Tank that can cause leaking, potentially delaying test results and exposing users to chemical and physical hazards.
Product
DxI 9000 Access Immunoassay Analyzer, REF C11137, vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2947-2024·2024-09-11
BD Pyxis QFill Medication Cabinet Software Issue Causes Incorrect Bin Labeling
A software bug in BD Pyxis QFill medication cabinet systems may print incorrect medication bin labels during restocking, potentially causing medication errors. Three units are affected.
Product
BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0653-2024·2024-09-11
Compounded Semaglutide Recalled Due to Lack of Sterility Assurance
ProRx LLC is recalling 1,960 vials of compounded semaglutide nationwide due to lack of assurance of sterility. The multiple-dose vials may not meet sterility standards for injectable medications.
Product
SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1786-2024·2024-09-11
Cheese Danish Recalled for Undeclared Milk Allergen
SSP America PHX, LLC is recalling Cheese Danish pastries distributed in Arizona. The product labels list cheese but fail to declare milk in the allergen statement, posing a risk to consumers with milk allergies.
Product
Cheese Danish in a clear plastic bag with a white paper label attached to the top of the plastic bag.
Category
Food
Distribution
1 state
HighFDA (Food)·F-1782-2024·2024-09-11
Pita Jungle Greek Salad Recalled for Undeclared Milk Allergen
SSP America PHX, LLC recalls Pita Jungle Greek Salad (11.8oz clamshell) because the product label listed feta but failed to declare milk as an allergen. Consumers with milk allergies should not consume this product.
Product
Pita Jungle Greek Salad packaged in 11.8oz plastic clamshell container.
Category
Food
Distribution
1 state
HighFDA (Food)·F-1776-2024·2024-09-11
Reser's Raspberry Parfait Desserts Recalled for Potential Spoilage
Reser's Fine Foods recalls 18 cases of Raspberry Parfait Desserts due to temperature abuse during transport that may have caused spoilage. Products with use-by date 12/4/2024 distributed in CA, IL, MN, ND, and SD.
Product
Item 71117.15207, Reser's Raspberry Parfait Desserts, refrigerated product, net wt. 8lb. There are 2 packs per case.
Category
Food
Distribution
5 states
HighFDA (Food)·F-1777-2024·2024-09-11
Refrigerated Pasta Salad Recalled for Temperature Abuse and Spoilage Risk
Reser's Fine Foods is recalling Stonemill Kitchens Green Goddess Pasta Salad due to potential spoilage from temperature abuse caused by a malfunctioning refrigeration unit. The product was distributed in CA, IL, MN, ND, and SD.
Product
Item 71117.18531, Stonemill Kitchens Green Goddess Pasta Salad, refrigerated product, net wt. 5lb. There are 2 packs per case.
Category
Food
Distribution
5 states
HighFDA (Food)·F-1779-2024·2024-09-11
Ground Cinnamon Recalled Nationwide for Elevated Lead Levels
MAMTAKIM Inc. is recalling ground cinnamon products distributed to nine states due to elevated lead content. The 15 g paper carton product carries code 10C035.
Product
Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton
Category
Food
Distribution
9 states
HighFDA (Food)·F-1774-2024·2024-09-11
Reser's Creamy Deluxe Potatoes Recalled for Temperature Abuse Risk
Reser's Fine Foods is recalling 182 cases of Potatoes Creamy Deluxe Special Request due to temperature abuse that may cause food spoilage.
Product
Item 71117.14446, Potatoes Creamy Deluxe Special Request, refrigerated product, net wt. 5lb. There are 4 packs per case.
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-2966-2024·2024-09-11
Impella 5.5 Pump Labeling Updated Due to Device Interaction
Abiomed updated Impella 5.5 cardiac pump labeling to document a potential interaction with Shockwave Coronary IVL Catheter during coronary procedures. No injuries have been reported.
Product
Impella 5.5 SmartAssist Set, JP; Product Code: 1000211;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2950-2024·2024-09-11
Anesthesia Vaporizer Adapter May Deliver Excessive Anesthetic Concentration
Sevoflurane vaporizer adapters used with Mindray A9 anesthesia systems may deliver higher-than-set anesthetic concentrations due to incomplete sealing. Patients could inhale excessive anesthetic, potentially causing drowsiness, vertigo, or in severe cases, neurological effects.
Product
Sevoflurane E_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number: 115-066756-00
Category
Medical Device
Distribution
0 states
HighNHTSA·23V781000·2024-09-11
2023 Nova Bus Transit Buses Recalled for Detachable Sun Visor Risk
Nova Bus is recalling certain 2023 LFS transit buses because the sun visor may detach from its bracket. A loose sun visor could distract the driver or block the windshield view, increasing crash risk.
Product
NOVA BUS — 2023 NOVA BUS LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2978-2024·2024-09-11
Medical Device Sample Holder Recalled for Adhesive Joint Failure
Beckman Coulter Power Express sample holders can fail at the adhesive joint between plastic socket and metal component. This may cause the metal part to detach inside the centrifuge, potentially damaging equipment and exposing lab staff to biohazardous material.
Product
Power Express, REF B90918
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V782000·2024-09-11
2023 Honda HR-V Seat Belt Pretensioner Assembly May Fail to Restrain
Honda is recalling certain 2023-2024 HR-V vehicles because the front seat belt pretensioners may be missing a rivet, which could cause the restraint to fail during a crash.
Product
HONDA — 2023 HONDA HR-V
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1775-2024·2024-09-11
Reser's Homestyle Gravy Recalled Due to Temperature Abuse
Reser's Fine Foods recalls Item 71117.14459 Gravy Homestyle due to temperature abuse during shipping. The product may become spoiled and pose food safety risks.
Product
Item 71117.14459, Gravy Homestyle, refrigerated product, net wt. 4lb. There are 3 packs per case.
Category
Food
Distribution
5 states

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11401–11425 of 31362