State

Vermont product recalls

72,984 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total: 1,983
Critical: 199
Severe: 409
Most recent: 2026-09-02

Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.

Which agencies issued them

These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7551–7575 of 74967

SevereFDA (Drugs)·D-0230-2025·2025-02-26
Phenylephrine HCl Injection Recall Due to Particulate Matter
Provepharm Inc. is recalling Phenylephrine HCl Injection vials (Lot 24020027) due to the presence of particulate matter. The affected medication was distributed nationwide.
Product
Phenylephrine HCl Injection, USP 100 mg/10 mL (10 mg/mL) vials, Rx only, Pharmacy Bulk Package (supplied as a single unit), Dist. by: Provepharm, Inc., Collegeville, PA 19426
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1153-2025·2025-02-26
Philips Azurion 3 M12 Medical Table Recalled for Patient Fall Risk
Philips is recalling Azurion 3 M12 patient tables due to possibility of patient falling from the table related to the mattress. The recall affects 263 units distributed in the US and internationally.
Product
Azurion 3 M12; Catalog numbers: (1) 722063, (2) 722221.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1159-2025·2025-02-26
Azurion 7 M12 Patient Tables: Fall Risk from Defective Mattress
Philips Azurion 7 M12 patient tables are recalled due to a mattress defect that could cause patients to fall. Approximately 1,837 units are affected globally.
Product
Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1149-2025·2025-02-26
Philips recalls Allura patient table mattress due to fall hazard
Philips is recalling Allura Xper patient table mattresses because a defect could cause patients to fall. The recall involves 302 units distributed globally.
Product
Allura Xper FD20/15; Catalog numbers: 722058
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1148-2025·2025-02-26
Philips Allura Xper FD20/10 Imaging System Patient Table Mattress Fall Risk
Philips is recalling the Allura Xper FD20/10 imaging system due to a defect in the patient table mattress that could allow patients to fall during procedures. The Class I recall affects 87 units distributed globally, including 22 in the US.
Product
Allura Xper FD20/10; Catalog numbers: 722029
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1143-2025·2025-02-26
Philips Allura Xper Fluoroscopy Device Patient Table Mattress Fall Risk
Philips Medical is recalling certain Allura Xper FD10/10 fluoroscopy systems because the patient table mattress could cause patients to fall during procedures. The recall affects devices worldwide.
Product
Allura Xper FD10/10; Catalog numbers: (1) 722005, (2) 722011, (3) 722027.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1158-2025·2025-02-26
Philips Azurion 7 B20 imaging system patient fall hazard from table mattress
Philips Azurion 7 B20 imaging systems are recalled because the patient table mattress may allow patients to fall. This FDA Class I recall affects 1,314 units distributed worldwide.
Product
Azurion 7 B20; Catalog numbers: (1) 722068, (2) 722226, (3) 722236.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1145-2025·2025-02-26
Philips Allura Xper FD20 Biplane Patient Fall Risk Recall
Philips Allura Xper FD20 Biplane x-ray tables are being recalled due to a mattress defect that could cause patients to fall. The recall affects 479 units distributed worldwide.
Product
Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1160-2025·2025-02-26
Azurion 7 M20 Patient Tables Recalled for Patient Fall Risk
Philips recalls Azurion 7 M20 patient tables due to a mattress defect that could cause patients to fall. Approximately 1,480 units in the US and 2,741 units overseas are affected.
Product
Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1147-2025·2025-02-26
Operating room table recalled due to mattress-related patient fall risk
Philips Allura Xper FD20 OR Table units (catalog numbers 722023, 722035) are recalled due to a mattress defect that could cause patients to fall during procedures.
Product
Allura Xper FD20 OR Table; Catalog numbers: (1) 722023, (2) 722035.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1146-2025·2025-02-26
Surgical Operating Table Recalled Due to Patient Fall Risk
Philips Medical Systems is recalling the Allura Xper FD20 Biplane OR Table due to a mattress defect that could cause patients to fall during surgery. 3 units are affected globally.
Product
Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1157-2025·2025-02-26
Philips Azurion 7 B12 examination tables recalled due to patient fall risk
Philips Medical Systems is recalling Azurion 7 B12 examination tables due to a mattress-related patient fall risk. The recall affects 602 total units, including 94 in the US and 508 internationally.
Product
Azurion 7 B12; Catalog numbers: (1) 722067, (2) 722225, (3) 722235 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1161-2025·2025-02-26
Philips Allura Centron patient table mattress defect poses fall risk
Philips is recalling Allura Centron patient examination tables due to a mattress defect that poses a fall risk. Eighty units have been distributed internationally.
Product
Cardio Vascular-Allura Centron; Catalog number: 722400 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1197-2025·2025-02-26
Hot Dog Patient Warming Mattress Connector Cable Deflection Recall
Augustine Temperature Management is recalling 4 units of the Hot Dog Patient Warming Mattress due to connector cable deflection that causes intermittent connection failures after approximately one year of use.
Product
Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 82 cm (32"), REF US501, to prevent or treat hypothermia
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1176-2025·2025-02-26
3M V.A.C. VIA Negative Pressure Wound Therapy System Recalled for Leak Alarm Malfunctions
KCI USA is recalling approximately 2,169 units of the 3M V.A.C. VIA negative pressure wound therapy system due to increased complaints about leak alarm malfunctions affecting certain units.
Product
3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit 65-Pack VIAKIT077D01/GB - V.A.C. VIA 7 Day Kit, Single Shipper
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0241-2025·2025-02-26
Atomoxetine 40 mg Capsules Recalled for N-Nitroso Impurity Above Limits
Glenmark Pharmaceuticals is recalling 233,040 bottles of Atomoxetine 40 mg capsules nationwide due to N-Nitroso impurity above FDA safety limits. Patients should check their medication bottles and contact their healthcare provider.
Product
ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1177-2025·2025-02-26
Irix-A Lumbar Fusion Implants Recalled for Incorrect Expiration Dates
XTANT Medical Holdings is recalling Irix-A Lumbar Fusion System implants due to incorrect expiration date labeling on sterile spacers. Fourteen units were distributed in Arizona, California, Colorado, Louisiana, Ohio, Texas, West Virginia, and Australia.
Product
Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC (Spacer Assy, 42 X 30 X 8¿, 11mm, PC (STERILE)) and Model Number X080-382819-08PC (Spacer ASSY, 38 X 28 X 8¿, 19mm, PC, (STERILE))
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0240-2025·2025-02-26
Prescription Drug Recall: Atomoxetine Capsules Due to Impurity
Glenmark Pharmaceuticals is recalling Atomoxetine 25mg capsules nationwide due to manufacturing deviations resulting in N-Nitroso Atomoxetine impurity above FDA limits. Consumers should contact their healthcare provider or pharmacist.
Product
ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1192-2025·2025-02-26
RayStation radiation therapy planning software density uncertainty computational defect
RayStation treatment planning software versions 4.5 through 2024B may incorrectly handle density uncertainty in radiation dose calculations for proton and light ion therapy. An inconsistency in three key functions could affect treatment planning accuracy.
Product
Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 6.1.1.2, 6.2.0.7, 6.3.0.6 Software Version: RayStation 6 Service Pack 1, 2 and 3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1203-2025·2025-02-26
Dexcom G6 glucose receiver may fail to deliver high or low alarms
Under rare conditions, the Dexcom G6 receiver may fail to send high or low glucose alarms due to a software error, potentially delaying detection of dangerous blood sugar levels.
Product
Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OR-001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1175-2025·2025-02-26
3M Prevena Plus Negative Pressure Therapy System Recalled for Leak Alarm Malfunctions
KCI USA is recalling 3M Prevena Plus wound therapy systems due to complaints about malfunctioning leak alarms. The recall affects 135,268 units distributed worldwide.
Product
3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US PRE3201US Prevena Plus Peel and Place 35 cm system Kit, US PRE3201 Prevena Plus Peel and Place 35 cm system Kit PRE4000US Prevena Plus 125 Therapy Unit, U
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1181-2025·2025-02-26
AnchorFast Guard Endotracheal Tube Fasteners Recalled Due to Tube Migration Risk
Hollister is recalling AnchorFast Guard endotracheal tube fasteners because decreased skin barrier wear time could cause tube migration. The recall affects multiple lot numbers distributed in the US and Canada.
Product
AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1186-2025·2025-02-26
RayStation radiation therapy planning software density uncertainty calculation inconsistency
RayStation radiation therapy planning software versions 4.5 through 2024B contain an inconsistency in density uncertainty handling when HU-to-mass density CT calibration curves are used. No illnesses or injuries have been reported.
Product
Brand Name: RayStation -Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113 and 9.0.1.142 Software Version: RayStation 8B, 8B Service Pack 1 and 2, 9A and 9A Service Pack 1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1195-2025·2025-02-26
RayStation Radiation Therapy Software Recalled for Dose Calculation Inconsistency
RayStation radiation therapy planning software is being recalled due to inconsistent handling of density uncertainty in dose calculations for proton and light ion treatment plans. The software defect may affect the accuracy of calculated radiation doses.
Product
Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 4.5.1.14, 4.7.2.5, 4.7.3.13, 4.7.4.4, 4.7.5.4 and 4.7.6.7 Software Version: RayStation 4.5.1, 4.7.2, 4.7.3, 4.7.4, 4.7.5 and 4.7.6
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0231-2025·2025-02-26
Atomoxetine Capsules Recalled for Elevated Nitrosamine Impurity
Glenmark Pharmaceuticals is recalling 70,032 bottles of Atomoxetine Capsules nationwide due to N-Nitroso impurity exceeding FDA recommended limits.
Product
ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
Category
Drug
Distribution
Distributed nationwide