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

12301–12325 of 27719

HighFDA (Devices)·Z-2022-2024·2024-06-12
GlideScope Core 15-inch Monitor Software Issue Causes Potential Image Loss
Verathon recalls 1,706 GlideScope Core 15-inch FHD monitors due to a software defect in versions v1.7 and earlier. The defect can cause loss or degradation of image when the monitor is used with other connectable devices.
Product
Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description: Serialized Monitor
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-2005-2024·2024-06-12
FLIXENE Vascular Graft Recalled for Slider Swivel Rod Separation
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reports of the slider swivel rod separating from the swivel core. The separation could affect device function during vascular procedures.
Product
FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1998-2024·2024-06-12
Vascular graft recall due to slider mechanism separation defect
Atrium Medical is recalling ADVANTA VXT vascular grafts due to separation of the slider mechanism. The defect affects over 53,000 units distributed worldwide and could compromise graft function.
Product
ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1951-2024·2024-06-12
FDA Recalls Atrium Medical Vascular Graft for Slider Separation Defect
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of the slider rod separating from the swivel core, which could impair proper device function.
Product
ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1955-2024·2024-06-12
Vascular Graft Component Separation Recall: ADVANTA VXT Slider
Atrium Medical recalls ADVANTA VXT vascular grafts due to separation of the slider swivel rod from its core. The defect affects 53,308 units distributed worldwide.
Product
ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2001-2024·2024-06-12
FDA Recalls ADVANTA VXT Vascular Grafts Due to Component Separation
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts because the Slider GDS Swivel Rod may separate from the Swivel Core. A total of 53,308 units are affected.
Product
ADVANTA VXT, 5-8X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1985-2024·2024-06-12
Vascular Graft Swivel Rod Separation Recalled Due to Component Failure
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of separation between the Slider GDS Swivel Rod and Swivel Core, which could affect device function.
Product
ADVANTA VXT, 8X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0534-2024·2024-06-12
Prescription migraine drug recalled for manufacturing impurity above FDA limit
Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate tablets for exceeding FDA acceptable limits of N-Nitroso Desmethyl Rizatriptan impurity. The recall affects 2,400 cartons distributed nationwide.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2023-2024·2024-06-12
BD SARS-CoV-2 Reagent Kits Recalled for False Negative Test Results
Becton Dickinson is recalling 2,061 kits of BD SARS-CoV-2 Reagents for BD MAX Systems because they may produce false negative results due to decreased enzyme activity. The kits were distributed nationwide and internationally.
Product
BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to detect SARS-CoV-2 in nasal, nasopharyngeal, oropharyngeal swab specimens, and saliva specimens.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1977-2024·2024-06-12
Vascular graft slider component separation reported in ADVANTA VXT
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units affected worldwide.
Product
ADVANTA VXT, 6X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2017-2024·2024-06-12
Vascular graft device recalled due to swivel rod separation
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reported separation of the swivel rod from the core component. This defect could compromise device function.
Product
FLIXENE, 4-7X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1981-2024·2024-06-12
Vascular graft recalled for reported swivel rod separation from core
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of the swivel rod separating from the swivel core. Patients and healthcare providers should contact the manufacturer for guidance.
Product
ADVANTA VXT, 8X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1975-2024·2024-06-12
ADVANTA VXT vascular graft recalled for swivel rod separation
Atrium Medical recalls ADVANTA VXT vascular grafts due to reports of swivel rod separation from the swivel core. Affected units distributed worldwide; healthcare providers should evaluate appropriate management.
Product
ADVANTA VXT, 6X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2011-2024·2024-06-12
Vascular Graft Component Separation Risk Triggers Worldwide Device Recall
Atrium Medical recalls FLIXENE vascular grafts due to reported separation of the Swivel Rod from the Swivel Core, creating gaps that could affect device function. Over 53,000 units worldwide are affected.
Product
FLIXENE, 6X30, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0535-2024·2024-06-12
FDA Recalls Rizatriptan Benzoate Tablets for Manufacturing Impurity
Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate 10mg tablets nationwide due to N-nitroso impurity levels exceeding FDA acceptable limits, affecting 13,296 cartons.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2006-2024·2024-06-12
Vascular graft component separation reported in FLIXENE Slider GDS devices
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reported separation between the Slider GDS Swivel Rod and Swivel Core, affecting 53,308 units distributed worldwide.
Product
FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2028-2024·2024-06-12
Philips Tempus LS-Manual Defibrillator may malfunction from electrical interference
Simultaneous ECG measurements with multiple devices can cause electrical interference that may prevent this defibrillator from functioning properly. The recall affects 1,745 units distributed nationwide.
Product
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1945-2024·2024-06-12
Proton Therapy System May Continue Irradiation When Accelerator Control Parameters Out of Tolerance
Ion Beam Applications' IBA Proton Therapy System PROTEUS 235 may continue delivering radiation when critical accelerator control parameters are outside defined tolerances. Affected users should contact the manufacturer regarding firmware updates.
Product
IBA Proton Therapy System - PROTEUS 235 - Designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1956-2024·2024-06-12
Vascular Graft Slider Component May Separate from Core
Atrium Medical is recalling ADVANTA VXT vascular grafts worldwide after reports of the slider swivel rod separating from the swivel core with a notable gap between components.
Product
ADVANTA VXT, 7X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1960-2024·2024-06-12
Vascular graft devices recalled due to slider component separation
Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.
Product
ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2010-2024·2024-06-12
Vascular Graft Device Recalled for Slider Rod Separation Risk
Atrium Medical Corporation is recalling approximately 53,308 FLIXENE vascular graft units worldwide due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating gaps that could affect device performance.
Product
FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1987-2024·2024-06-12
Advanta VXT vascular grafts recalled for swivel rod separation
Atrium Medical Corporation is recalling the Advanta VXT vascular graft due to reports of the swivel rod separating from the swivel core. The recall affects approximately 53,308 units distributed in the United States and worldwide.
Product
ADVANTA VXT, 7X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2008-2024·2024-06-12
FLIXENE vascular graft recalled for slider separation defect
Atrium Medical recalls FLIXENE vascular grafts due to reported separation between the slider rod and swivel core. Affected grafts may fail to function properly if deployed.
Product
FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1941-2024·2024-06-12
Synchro2 Guidewires: PTFE coating damage from improper backloading technique
Stryker Neurovascular is recalling certain lots of Synchro2 Guidewires due to PTFE coating damage caused by backloading through an introducer accessory with manufacturing variations. Affected users should discontinue the backloading technique.
Product
The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014 in. The guidewires are compatible with existing microcatheters used in common procedures such as
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2018-2024·2024-06-12
Vascular graft recalled due to swivel rod separation risk
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. The recall affects 53,308 units distributed worldwide.
Product
FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide

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12301–12325 of 27719