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

576–600 of 5642

SevereFDA (Food)·F-0400-2025·2025-01-22
Cucumbers sold in multiple states recalled due to Salmonella contamination risk
Wholesale Produce Supply is recalling cucumbers sold in multiple Midwest states and Canada due to potential Salmonella contamination. Consumers should not eat the affected product and should dispose of it safely.
Product
Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in the following pack sizes: 1. 5 lb. pack 2. 6 ct individual items per case. 3. 12 ct individual items per case. 4. 24 ct individual items per case. 5.
Category
Food
Distribution
9 states
SevereFDA (Devices)·Z-0821-2025·2025-01-22
Neo-Tee Resuscitator Spring Defect May Impair Pediatric Ventilation
Mercury Medical is recalling the Neo-Tee T-Piece Resuscitator due to an undersized spring in the circuit flow controller that may prevent reaching proper pressure ranges, potentially impairing emergency ventilation.
Product
Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810, 1050811, 1050814, 1050832, 1050839, 1050840, 1050841, 1050842
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0390-2025·2025-01-22
Boar's Head Hummus Vegetable Platter recalled for potential Salmonella
Boar's Head Hummus Vegetable Platter 5 lb. packages may contain cut cucumbers contaminated with Salmonella. The recall affects 121 units distributed in AZ, CO, LA, NM, TX, UT, and WY.
Product
BOAR'S HEAD HUMMUS VEG PLATTER MED, 5 lb., packaged in a plastic container with a plastic lid, UPC 42421-61547
Category
Food
Distribution
7 states
SevereFDA (Devices)·Z-0716-2025·2025-01-22
Endoscopic Access Overtube Sheath Recalled Due to Pressure Buildup Risk
Trokamed GmbH is recalling an endoscopic access overtube sheath due to risk of intrarenal pressure buildup when inflow speed is too fast. No injuries reported.
Product
Sheath, 18 Fr., 160 mm (REF: WA2PS18L), gastroenterology-urology endoscopic access overtube.
Category
Medical Device
Distribution
1 state
SevereFDA (Food)·F-0396-2025·2025-01-22
Diced Cucumber from First Quality Produce Recalled for Salmonella
First Quality Produce is recalling diced cucumber (5-lb trays) due to potential Salmonella contamination. The recalled product was distributed to consignees in California and was not sold at retail.
Product
Cucumber Diced; 5-lb plastic trays Brand: First Quality Produce
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-0765-2025·2025-01-22
Medline Fluid Delivery Sets Recalled Due to Assembly Error
Medline Fluid Delivery Sets were incorrectly assembled with macro drip chambers instead of required micro drip chambers. The macro chamber delivers three times more fluid per drop, creating a risk of dosing errors.
Product
Medline Fluid Delivery Set with Drip Chamber: 1) MTO,135,YELLOW,MICRO,SPK-MAIMONIDES, Item Number: 60130527; 2) MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH, Item Number: 65111341; 3) MTO,ANGIO,SINGLE,SPIKE,KIT, Item Number: 65232486; 4) MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM, Item
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0714-2025·2025-01-22
Endoscopic Access Overtube Recalled for Risk of Obstruction and Pressure Buildup
Trokamed is recalling a 20 Fr. endoscopic access overtube due to risk of obstruction and dangerous kidney pressure buildup during procedures. If inflow speed is too quick, rapid fluid flow can restrict outflow and cause intrarenal pressure to accumulate.
Product
Sheath, 20 Fr., 160 mm (REF: WA2PS20L), gastroenterology-urology endoscopic access overtube.
Category
Medical Device
Distribution
1 state
SevereFDA (Food)·F-0398-2025·2025-01-22
Daily Veggies Enoki Mushroom Recalled for Possible Listeria Contamination
New Age International recalls Daily Veggies Enoki Mushrooms due to potential Listeria monocytogenes contamination. The product was distributed in New York and Maryland; consumers should not consume it.
Product
Daily Veggies Enoki Mushroom, 200g Product of Korea UPC Codes: 8809159458890
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0402-2025·2025-01-22
Pinsarella Roman Pizza Recalled for Undeclared Wheat and Soy Allergens
Pinsarella Food LLC is recalling Roman Pizza products due to undeclared wheat and soy allergens. The affected products were distributed to restaurants in California through food distributors.
Product
Pinsarella Roman Pizza, POL127-24, UPC 6 08539 14655 0 -Oval, 12x7/ 7.0 Oz, Parbaked, 6 units per bag, 24 units per box., UPC 1 98715 69442 0 - Oval, 14x9/ 10.6 Oz, Parbaked, 6 units per bag, 24 units per box., UPC 6 08539 33371 4 - Round, 8" / 5.0 Oz, Parbaked, 6 units per bag,
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0388-2025·2025-01-22
Small Veggie Platter Recalled for Potential Salmonella Contamination
The Kroger Co is recalling Small Veggie Platters (32 oz) because they may contain cut cucumbers previously recalled due to potential Salmonella contamination.
Product
SMALL VEGGIE PLATTER, 32 oz., packaged in a plastic container with a plastic lid, UPC 41573-26809
Category
Food
Distribution
7 states
SevereFDA (Devices)·Z-0829-2025·2025-01-22
Impella RP Heart Pump Recalled Due to Optical Sensor Damage Risk
Abiomed is recalling 1,560 units of the Impella RP with SmartAssist pump due to risk of optical sensor damage from device interactions. Damaged sensors may cause temporary or permanent pump malfunction.
Product
Impella RP with SmartAssist; Product Number: 0046-0035;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0885-2025·2025-01-22
Welch Allyn Life2000 Ventilator Battery Charger May Cause Device Inoperability
Baxter Healthcare is recalling 946 Welch Allyn Life2000 ventilators due to a battery charger defect that can trigger an alarm and render the device inoperable.
Product
Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0764-2025·2025-01-22
Medline Fluid Delivery Sets incorrectly assembled with wrong drip chamber
Medline fluid delivery sets were assembled with a macro drip chamber instead of the required micro drip chamber, delivering three times more fluid per drop and risking patient fluid overload.
Product
Medline Fluid Delivery Set with Drip Chamber: 1) FDS,135,CHMN,W/F,MLL,RC(2),PG, Item Number 99000069; 2) FDS,135,NV,MICRO-CHAMBER,W/FILTER,BLUE, Item Number 949000222; 3) FDS,135,NV,MICRO-CHAMBER,W/FILTER,GREEN, Item Number 949000224; 4) FDS,135,NV,MICRO-CHAMBER,W/FILTER,RE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0827-2025·2025-01-22
VISIONIST CRT-P Pacemakers Recalled Due to Battery Impedance Risk
Certain VISIONIST CRT-P pacemakers with latent high battery impedance may initiate Safety Mode unexpectedly during normal operations. Manufactured before September 2018, 156,329 units were distributed worldwide.
Product
VISIONIST CRT-P, EL (Model Number U225 and U226) and EL MRI (Model Number U228)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0905-2025·2025-01-22
Olympus MAJ-891 Forceps Recalled for Potential Biomaterial Retention During Reprocessing
Olympus recalls the MAJ-891 endoscope forceps/irrigation plug nationwide because improper reprocessing may leave biomaterial inside the device, creating a contamination risk.
Product
Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog Number: MAJ-891. This instrument is designed to be attached to the instrument channel port of Olympus endoscopes to allow both irrigation and the use of endo-therapy accessories.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0826-2025·2025-01-22
CRT-P Pacemakers Recalled for Potential Safety Mode Initiation Risk
Boston Scientific's ACCOLADE Family pacemakers, including VALITUDE CRT-P models, are recalled due to battery impedance defects that could trigger unintended Safety Mode during normal operation.
Product
VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0831-2025·2025-01-22
Dialysis Blood Circuit May Cause Excessive Fluid Removal
The AquaFlexFlow UF 500 Plus blood circuit may malfunction and remove excessive fluid from patients, causing a dangerous drop in blood volume. This risk is especially dangerous for pediatric patients.
Product
nuwellis AquaFlexFlow UF 500 Plus, REF 114156, Catalog Number A06163, extracorporeal blood circuit which is used with the Aquadex SmartFlow or Aquadex FlexFlow System
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·25091·2025-01-16
Northern Tool Adjustable Shop Stools Recalled for Fall Hazard
Northern Tool + Equipment is recalling about 51,770 Adjustable Swivel Shop Stools with Backrests due to weld failure. The company has received 271 incident reports, including 18 injuries from falls.
Product
Northern Tool + Equipment Adjustable Swivel Shop Stools with Backrests
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0384-2025·2025-01-15
Baker's Source Cornbread Mix Recalled for Undeclared Egg Allergen
Baker's Source Traditional Cornbread Mix is being recalled due to undeclared egg allergen. The 210,960-pound recalled quantity was distributed across eight states and poses a risk to consumers with egg allergies.
Product
235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption & mix with water and bake Shelf Stable Dry Mix, 1 Year Shelf Life
Category
Food
Distribution
0 states
CriticalFDA (Drugs)·D-0179-2025·2025-01-15
Clonazepam Orally Disintegrating Tablets Carton Mislabeled on Declared Strength
Endo USA recalls 8,029 cartons of Clonazepam 0.125 mg tablets nationwide due to incorrect carton labeling, although the tablets in the blister strips have the correct strength.
Product
CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0763-2025·2025-01-15
Large Volume Pump model LVP-0004 recalled for potential pneumatic valve failure
Fresenius Kabi is recalling 1,520 Ivenix infusion pumps (model LVP-0004) due to potential pneumatic valve failure that may stop active infusions or prevent pump operation. Affected units were distributed to healthcare facilities in six U.S. states.
Product
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Category
Medical Device
Distribution
6 states
SevereFDA (Drugs)·D-0181-2025·2025-01-15
Clonazepam Tablets Recalled Due to Carton Labeling Error
Endo USA, Inc. is recalling 22,513 cartons of clonazepam tablets due to incorrect strength labeling on some carton exteriors. The actual tablets inside have correct labeling.
Product
CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0378-2025·2025-01-15
Greek yogurt tzatziki products recalled for potential salmonella
US Foods Chef's Line and Nick The Greek tzatziki products distributed across multiple states are being recalled due to potential salmonella contamination. Consumers should not consume these products.
Product
US Foods Chef's Line Greek Yogurt Tzatziki 4lbs tub, UPC 758108679962, SKU SAL519448, 2 tubs per case. Nick The Greek Tzatziki Pail, 42lbs pail, UPC 10075365177787, SKU SA000084
Category
Food
Distribution
27 states
SevereFDA (Drugs)·D-0178-2025·2025-01-15
Clonazepam tablets recalled for incorrect carton labeling
Endo USA is recalling approximately 9,816 cartons of Clonazepam 2 mg tablets due to incorrect strength labeling on the carton exterior. The blister strips inside contain the correct formulation.
Product
CLONAZEPAM — CLONAZEPAM (CLONAZEPAM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0177-2025·2025-01-15
Herbal Capsules Recalled Nationwide for Undeclared Pharmaceutical Ingredients
Herbal capsules sold nationwide have been recalled after the FDA found undeclared medications inside. The product contained furosemide, dexamethasone, and chlorpheniramine without proper labeling.
Product
Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang, Malasia.
Category
Drug
Distribution
Distributed nationwide

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