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

2326–2350 of 36523

SevereFDA (Devices)·Z-1866-2025·2025-06-18
Z-800F Infusion System Recall Due to Unvalidated Software Versions
Zyno Medical LLC is recalling the Z-800F Infusion System because unreleased software versions were installed on distributed devices without verification or validation. This poses a risk to patients receiving intravenous infusion therapy.
Product
Z-800F Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1932-2025·2025-06-18
Philips Intera 1.5T Explorer/Nova Dual MRI Gradient Coil Fire Risk
Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a gradient coil component that may overheat, produce smoke, or ignite, risking patient and operator injury.
Product
Intera 1.5T Explorer/Nova Dual Product Number: 781108;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0466-2025·2025-06-18
Dietary Supplement ULTRA ARMOR Recalled for Undeclared Drug Ingredients
ULTRA ARMOR dietary supplement, distributed by Health Fixer, is recalled nationwide because it contains undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0037-2025·2025-06-18
Cucumber Sliced Unpeeled 2 oz. Pack Recalled for Salmonella
TGD Cuts, LLC is recalling Cucumber Sliced Unpeeled (Item #7065, UPC #840219170657) in 2 oz. packs due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.
Product
Cucumber Sliced Unpeeled, Pack Size 50, 2 oz. , 50 per case
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-1963-2025·2025-06-18
Microtek Patient Drape Adapter Plug Kits Recalled for Non-Sterile Labeling
Microtek Medical is recalling Patient Drape adapter plug kits (models AP6MMN and AP8MMN) because non-sterile products were labeled as sterile. The affected adapters are used to connect drain hoses to fluid management devices.
Product
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN Patient Drape, 8mm Adapter Plug Kit REF AP8MMN UDI code: (01)10748426139429 These adapters function as accessories for a device or drape, serving to
Category
Medical Device
Distribution
20 states
SevereFDA (Drugs)·D-0464-2025·2025-06-18
MALEXTRA Dietary Supplement Recalled for Undeclared Pharmaceutical Ingredients
MALEXTRA Recharge with Extra dietary supplement is being recalled nationwide because laboratory testing found undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil in the product.
Product
MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0467-2025·2025-06-18
Male Ultra Pro dietary supplement recalled for undeclared pharmaceutical ingredients
Male Ultra Pro capsules are being recalled because laboratory testing found undeclared propoxyphenylsildenafil and sildenafil. The product was marketed without an approved New Drug Application.
Product
Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1915-2025·2025-06-18
Covidien Newport HT70 and HT70Plus Ventilators Capacitor Failure Recall
Covidien is recalling Newport HT70 and HT70Plus ventilators due to capacitor failures that may cause the device to shut down unexpectedly or fail to alarm, risking respiratory failure and oxygen deprivation in patients.
Product
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU, HT70M-WW-NA, HT70-SY-EU. Newport HT70Plus Ventilator, REF: HT70PM-ES-EU, HT70PM-ES-NA, HT70PM-JP-NA, HT70PM-PT-BR, HT70PM-SY-AS, DLHT70PM-WW-NA, HT70PM-SY-NA, HT70PM-SY-
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1867-2025·2025-06-18
Z-800W Infusion System Recalled for Unvalidated Software Installation
Zyno Medical LLC is recalling the Z-800W Infusion System because unreleased software versions were installed on devices without verification or validation.
Product
Z-800W Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1972-2025·2025-06-18
BD Texium Closed System Drug Transfer Devices May Leak at Connector
BD Texium closed system drug transfer devices in multiple sizes may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, exposure to hazardous drugs, and underdosing.
Product
BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1930-2025·2025-06-18
Philips Intera 1.5T Achieva Nova MRI Systems Gradient Coil Fire Risk
Philips is recalling certain Intera 1.5T Achieva Nova MRI systems due to a gradient coil component that can overheat, potentially causing smoke or fire with risk of burns, smoke inhalation, or asphyxia.
Product
Intera 1.5T Achieva Nova Product Number: 781172;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0032-2025·2025-06-18
Jean's Classy Fresh Salsa Mild recalled for Salmonella contamination
TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Mild (12 oz. glass jars) due to Salmonella contamination. The product was distributed in Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.
Product
Jean's Classy Fresh Salsa, Mild, 12 oz. Glass Jars, 6 per case.
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0027-2025·2025-06-18
Cucumber Super Selec Repacked by Lipman Produce Recalled for Salmonella
Lipman Family Farms is recalling Cucumber Super Selec products due to potential Salmonella contamination. The cucumbers were distributed across multiple states.
Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
Category
Food
Distribution
18 states
SevereFDA (Devices)·Z-1969-2025·2025-06-18
Azurion R1.x and R2.x X-ray systems software communication issue
Philips Medical Systems has recalled Azurion R1.x and R2.x X-ray systems worldwide due to a software issue that can cause loss of imaging functionality and delay treatment, potentially resulting in serious harm or death in patients undergoing urgent or complex interventions.
Product
Azurion R1.x and R2.x systems; Model Numbers: (1) 722063, (2) 722064, (3) 722067, (4) 722068, (5) 722078, (6) 722079, (7) 722221, (8) 722222, (9) 722223, (10) 722224, (11) 722225, (12) 722226, (13) 722227, (14) 722228, (15) 722280, (16) 722281, (17) 722282; Software Version: Al
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0030-2025·2025-06-18
Cucumber Super Selec from Lipman Produce Recalled for Salmonella Risk
Lipman Family Farms is recalling Cucumber Super Selec products due to potential Salmonella contamination. The affected cucumbers were distributed across multiple states.
Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
Category
Food
Distribution
18 states
SevereFDA (Devices)·Z-1928-2025·2025-06-18
Philips Achieva XR MRI systems recall for fire hazard
Philips Achieva XR MRI systems may have a gradient coil component failure that can generate heat, smoke, and fire. The risk to patients and operators includes inhalation of smoke, burns, and asphyxia.
Product
Achieva XR Product Numbers: (1) 781153, (2) 781253;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0024-2025·2025-06-18
East Coast Fresh Greek Pasta Salad Kit recalled for Salmonella risk
Sysco Corporation is recalling East Coast Fresh Greek Pasta Salad Kits due to potential Salmonella contamination in cucumbers. No illnesses have been reported.
Product
KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit 1/5lb W/Pasta ALL LOT CODES KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit 1/5lb W/Pasta ALL LOT CODES KITGREEKPASTA51 1/5# EAST COAST FRESH Greek Pasta Salad Kit 1/5lb W/Pasta (RF) ALL LOT CODES
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0036-2025·2025-06-18
Cucumber Sliced Unpeeled recalled for Salmonella contamination
TGD Cuts, LLC is recalling Cucumber Sliced Unpeeled (5 lbs. per case, Item #6073) distributed to MD, PA, NC, VA, and NJ due to Salmonella contamination.
Product
Cucumber Sliced Unpeeled, Pack Size 5 lbs. , 1 per case
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0023-2025·2025-06-18
East Coast Fresh Salsa Products Recalled for Potential Salmonella Contamination
Sysco Corporation is recalling multiple East Coast Fresh salsa products distributed across 18 states and Puerto Rico due to potential Salmonella contamination in cucumbers used in the product.
Product
RTSALSA1LB 1# EAST COAST FRESH Salsa Cup - 1 lb ALL LOT CODES SAL20 5# EAST COAST FRESH EC-Salsa- Fresh 5# ALL LOT CODES SAL210 6/1# EAST COAST FRESH Salsa- Fresh Retail 6x1# (E) ALL LOT CODES SAL45 20# EAST COAST FRESH EC-Salsa- Fresh 20# ALL LOT CODES SAL48 7# EAST COAST FRESH
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0035-2025·2025-06-18
Jean's Classy Fresh Salsa Recalled Due to Salmonella Contamination
Jean's Classy Fresh Salsa, Mild (5 lbs.) is being recalled due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.
Product
Jean's Classy Fresh Salsa, Salsa, Mild 5 lbs. 1 per case .
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0038-2025·2025-06-18
Cucumber Sliced and Grape Tomato Packs Recalled for Salmonella Contamination
TGD Cuts, LLC is recalling Cucumber Sliced/Grape Tomato 50/2oz. packs due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.
Product
Cucumber Sliced/Grape Tomato 50/2oz. Pack, 50 per case
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-1921-2025·2025-06-18
SOLTIVE Premium SuperPulsed Laser System surgical instrument thermal incident
Olympus is recalling the SOLTIVE Premium SuperPulsed Laser System due to risk of thermal incidents including smoke, sparks, burning, or flames during clinical use caused by fiber fracturing.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and f
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0020-2025·2025-06-18
Created Fresh Chicken Salad Sandwich Recalled for Salmonella Risk
Sysco Corporation is recalling Created Fresh Chicken Salad on Everything Ficelle sandwiches due to potential Salmonella contamination from cucumbers used in the product.
Product
HKSAC168 6/5.76 OZ. CS CREATED FRESH Sub- Chicken Salad on Everything Ficelle- 6/6oz ALL LOT CODES HKSAN168 1/5.76OZ CREATED FRESH Sub- Chicken Salad on Everything Ficelle ALL LOT CODES HKSAC168 6/5.76 OZ. CS Created Fresh Sub- Chicken Salad on Everything Ficelle- 6/6oz ALL LOT C
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0028-2025·2025-06-18
Cucumber 5lb Cases Recalled Due to Potential Salmonella Contamination
Lipman Family Farms is recalling Cucumber 5lb cases distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Product
Cucumber 5lb Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0097-2025·2025-06-18
Non Fat Dry Milk Recalled for Potential Salmonella Contamination
Crystal Creamery Inc. is recalling non fat dry milk due to potential Salmonella contamination. The affected product was distributed in California and Texas.
Product
NON FAT DRY MILK. "LOW HEAT SPRAY PROCESS GRADE A NON FAT DRY MILK MADE FROM PASTERUIZED MILK, NET WEIGHT 25.00 KG, PRODUCT OF U.S.A."
Category
Food
Distribution
2 states

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2326–2350 of 36523