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

8001–8025 of 89535

HighFDA (Food)·F-0593-2025·2025-03-12
Hummus Recall: Plastic Fragments Found in King Harvest Chipotle Hummus
Pacific Coast Fresh CO is recalling 1953 cups of King Harvest Chipotle Hummus due to potential plastic fragments in the product. The affected hummus was distributed in Idaho, Oregon, and Washington.
Product
Item #96517, King Harvest Chipotle Hummus, net wt. 10oz., UPC 025726 31007 3, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Food)·F-0600-2025·2025-03-12
Food Recall: King Harvest Sundried Tomato Hummus, Plastic Fragments
Pacific Coast Fresh Co is recalling King Harvest Sundried Tomato Hummus due to potential plastic fragment contamination. The product was distributed in Idaho, Oregon, and Washington.
Product
Item #96528 and 32899, King Harvest Sundried Tomato Hummus, net wt. 10oz., UPC 025726 31118 6, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1249-2025·2025-03-12
Access Erythropoietin Reagent Lot Produces Falsely Decreased Test Results
Beckman Coulter's Access Erythropoietin (EPO) reagent lot 439363 produces falsely decreased test results with patient samples. Affected results may lead to improper diagnosis or unnecessary repeat testing.
Product
Access Erythropoietin (EPO), Catalog Number - A16364 a glycoprotein (~30,400 Daltons) produced primarily by the kidney, is the principal factor regulating red blood cell production (erythropoiesis) in mammals. Renal production of EPO is regulated by changes in oxygen availabil
Category
Medical Device
Distribution
24 states
HighNHTSA·25C004000·2025-03-12
Dorel Recalls Safety 1st Child Seats Due to Incorrect Height Labeling
Dorel Juvenile Group is recalling specific Safety 1st 3-in-1 child seats because the forward-facing installation label incorrectly states the height range, which may lead to improper restraint.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1267-2025·2025-03-12
MIM Radiological Imaging Software Versions May Generate Incorrect Diagnostic Values
MIM radiological software versions 7.2.0-7.2.6 may produce incorrect readings when fusing images with different fields of view, which could affect diagnostic accuracy.
Product
MIM software; System, Image Processing, Radiological
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0599-2025·2025-03-12
Spinach hummus recalled for plastic fragment contamination
Pacific Coast Fresh Co is recalling King Harvest Spinach Hummus due to plastic fragment contamination. Affected products were distributed in Idaho, Oregon, and Washington with expiration dates in February 2025.
Product
Item #96527 and item #32902, King Harvest Spinach Hummus, net wt. 10oz., UPC 025726 31108 7, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1259-2025·2025-03-12
MiniMed Insulin Pumps Recalled for Abnormal Insulin Delivery During Flight
MiniMed insulin pumps may deliver abnormal insulin doses during aircraft takeoff and landing due to air pressure changes, risking severe blood sugar fluctuations, seizures, and potentially fatal complications.
Product
MiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1250-2025·2025-03-12
TBS iNsight bone density software calculation variability on Hologic machines
TBS iNsight medical device software may produce inconsistent calculation results when operating on Hologic Horizon bone densitometers, particularly when comparing fast array scans to standard array scans.
Product
Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number: TBS iNsight v3.x / pn: OS-TBSi Software Version: V3.x: (1) V3.1.2, (2) V3.1.1, (3) V3.1.0, (4)V3.0.0 Product Description: TBS iNsight is a class II Medical Device software that is installed on bone densitom
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-1261-2025·2025-03-12
Medtronic MiniMed insulin pump recalled for air pressure-triggered delivery defect
Medtronic MiniMed insulin pumps can deliver abnormal insulin doses during air pressure changes in airplane travel, risking severe hypoglycemia or hyperglycemia and serious complications.
Product
MiniMed insulin pump, REF: 670G (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1268-2025·2025-03-12
Heat Moisture Exchanger Connector Occlusion May Impair Ventilation
Kung Shin Plastics' CircuitGuard ThermoFlo Filter may have plastic obstructing the machine-side connector, preventing proper ventilation bag operation and risking oxygen deprivation during manual ventilation.
Product
CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger, Bacterial Viral Filter w O2 Port and Elbow (Model/Catalogue number: SK200CPE / 6126)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0592-2025·2025-03-12
King Harvest Black Olive Hummus Recalled Due to Plastic Fragments
King Harvest Black Olive Hummus (10 oz) has been recalled due to the presence of plastic fragments. The voluntary recall affects 4,019 cups distributed in Idaho, Oregon, and Washington.
Product
Item #96514 and item #32903, King Harvest Black Olive Hummus, net wt. 10oz., UPC 025726 31121 6, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1260-2025·2025-03-12
Medtronic MiniMed Insulin Pumps Recalled for Abnormal Delivery During Air Pressure Changes
Medtronic is recalling MiniMed insulin pumps that malfunction during airplane takeoff and landing due to air pressure changes. The defect can cause abnormal insulin delivery, leading to severe hypoglycemia, hyperglycemia, seizure, coma, or death.
Product
MiniMed insulin pump, REF: 640G (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1258-2025·2025-03-12
MiniMed Insulin Pumps Recalled for Abnormal Delivery During Air Travel
Medtronic recalled MiniMed insulin pumps due to abnormal delivery caused by air pressure changes during airplane flights. The defect can cause severe hypoglycemia or hyperglycemia, potentially leading to seizure, coma, or death.
Product
MiniMed insulin pump, REF: 620G (MMT-1750)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1262-2025·2025-03-12
Medtronic MiniMed insulin pump recalled for abnormal delivery during air pressure changes
Medtronic MiniMed insulin pumps may deliver insulin abnormally during airplane take-off or landing due to air pressure changes, risking severe low or high blood sugar emergencies.
Product
MiniMed insulin pump, REF: 700G (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0602-2025·2025-03-12
Food Recall: Plastic Fragments in King Harvest Toasted Sesame Hummus
Pacific Coast Fresh CO is recalling King Harvest Toasted Sesame Hummus (10oz) due to plastic fragments. Affected products were distributed in Idaho, Oregon, and Washington with expiration dates from February 3 to 23, 2025.
Product
Item #96526 and item #32900, King Harvest Toasted Sesame Hummus, net wt. 10oz., UPC 025726 31122 3, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0256-2025·2025-03-12
Nelarabine prescription injection recalled due to failed quality specifications
Zydus Pharmaceuticals is recalling 1,893 vials of Nelarabine Injection (250 mg/50 mL) due to failed quality specifications for impurities and degradation. Patients should contact their healthcare provider about the recall.
Product
NELARABINE — NELARABINE (NELARABINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1295-2025·2025-03-12
AURORA Surgiscope System Obturator May Break or Separate
Integra LifeSciences Corp. is recalling AURORA Surgiscope Systems (models ASX15/60 and ASX15/80) because the obturator component may break or separate during surgical use. Healthcare facilities should discontinue use and contact the manufacturer for instructions.
Product
AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. Manufacturer's Product Numbers (Catalog Number): (1) ASX15/60 and (2) ASX15/80
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0595-2025·2025-03-12
Hummus Recall: Plastic Fragments in King Harvest Jalapeno Hummus
Pacific Coast Fresh Co is recalling 10,374 cups of King Harvest Jalapeno Hummus due to plastic fragments. The affected product was distributed in Idaho, Oregon, and Washington with expiration dates in February and March 2025.
Product
Item #96521, item #32896, and item #32898, King Harvest Jalapeno Hummus, net 10oz., UPC 025726 31004 2, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Food)·F-0598-2025·2025-03-12
King Harvest Roasted Garlic Hummus recalled for plastic fragment contamination
King Harvest Roasted Garlic Hummus is being recalled for possible plastic fragment contamination. The voluntary recall affects 9,588 cups distributed in Idaho, Oregon, and Washington.
Product
Item #96520 and item #32898, King Harvest Roasted Garlic Hummus, net wt. 10oz., UPC 025726 21114 1, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.
Category
Food
Distribution
3 states
HighFDA (Drugs)·D-0252-2025·2025-03-12
Ferrous Sulfate Oral Syringes Recalled Due to Leakage Defect
Safecor Health is recalling 1535 Ferrous Sulfate 7.5 mg oral syringes distributed nationwide due to leakage observed during repackaging. The defective delivery system could result in improper dosing of the iron supplement.
Product
Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe, Delivers: 0.5 mL, Iron Supplement Drops, Mfg by: Akron Pharma, Pkg by: Safecor, Columbus, OH 43204. NDC: a) 71399748005, b) 39328055750, c) 69618007059.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0253-2025·2025-03-12
Lorazepam Oral Syringes Recalled Due to Defective Delivery System Causing Leakage
Safecor Health, LLC is recalling Lorazepam 0.5 mg oral syringes nationwide due to a defective delivery system that causes leakage after repackaging.
Product
Lorazepam 0.5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Concentrate, Rx Only, Refrigerate, Mfg by: PAI, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00054353244, b) 00121077001, c) 65162068784.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0249-2025·2025-03-12
Morphine Sulfate Tablets Recalled Over Failed Dissolution Specifications
Sun Pharmaceutical is recalling Morphine Sulfate Extended-Release 100 mg tablets (lot AD16615) because they fail dissolution specifications, potentially resulting in unpredictable drug delivery.
Product
MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1293-2025·2025-03-12
Alcon Custom Pak surgical packs mislabeled as latex-free despite containing latex
Alcon surgical procedure packs contain latex but are labeled as latex-free, creating risk of allergic reaction for patients with latex sensitivity. The company is recalling 2,511 affected units.
Product
Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-17, 14764-09, 13194-16, 17069-09
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1276-2025·2025-03-12
Osstem dental implant abutments mislabeled on patient chart stickers
Hiossen is recalling 119 Osstem dental implant abutments because patient chart stickers incorrectly identify product versions. ET Rigid and ET Multi abutments are labeled backwards, potentially leading to selection of the wrong abutment size.
Product
Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is intended for use with a dental implant to provide suport for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETMTA505RV1
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25E018000·2025-03-11
Cummins Recalls PowerDrive 7000 Electric Drivetrains Due to Battery Short Circuit Risk
Cummins is recalling high voltage battery packs in certain PowerDrive 7000 electric drivetrains because internal fasteners may detach, causing short circuits, loss of power, or fire.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
Category
Vehicle
Distribution
Distributed nationwide

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8001–8025 of 89535