State

Vermont product recalls

20,083 recalls have nationwide distribution and so reach Vermont. 0 additional recalls listed Vermont specifically in their distribution scope.

About recalls in Vermont

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Vermont consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

5851–5875 of 20083

CriticalFDA (Devices)·Z-1070-2025·2025-02-26
Vascular Tack Endovascular System recalled for deployment and migration risks
Spectranetics' Intact Vascular Tack Endovascular System may fail to deploy properly or migrate in blood vessels, potentially causing ischemia and requiring additional intervention.
Product
Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm), 150cm, REF: 154150041; Tack, 4F Gen 1.5, 150cm CE, REF: 154150042; Tack, 4F Gen 1.5, 90cm CE, REF: 154090042 (6F, 3.5 - 6.0mm), 135cm, REF: 15613
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1156-2025·2025-02-26
Philips Azurion 5 M20 tables recalled due to patient fall risk
Philips is recalling Azurion 5 M20 imaging tables worldwide due to a mattress defect that could cause patients to fall from the table. This FDA Class I recall involves 632 units.
Product
Azurion 5 M20; Catalog numbers: (1) 722228, (2) 722232 (OUS ONLY), (3) 722281 (OUS ONLY).
Category
Medical Device
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-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-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-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-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-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-1151-2025·2025-02-26
Philips Allura CV20 Patient Table: Fall Risk from Mattress Defect
Philips is recalling the Allura CV20 patient table due to a mattress defect that could allow patients to fall. The recall affects 111 units distributed worldwide.
Product
Allura CV20; Catalog numbers: 722031
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-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-1142-2025·2025-02-26
Medical imaging device patient table mattress may cause patient falls
Philips is recalling Allura Xper FD10 imaging devices because the patient table mattress may not securely hold patients during procedures, creating a fall hazard. The recall affects 2,274 units worldwide, including 459 in the U.S.
Product
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1155-2025·2025-02-26
Philips Azurion 5 M12 Patient Table Recalled for Fall Risk
Philips Medical Systems is recalling Azurion 5 M12 imaging tables due to a mattress defect that could allow patients to fall from the table.
Product
Azurion 5 M12; Catalog numbers: (1) 722227, (2) 722231 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0245-2025·2025-02-26
Fentanyl Transdermal Patches Recalled for Defective Delivery System
Alvogen has recalled Fentanyl Transdermal System patches (25 mcg/h) nationwide due to a manufacturing defect where patches may be stacked together in a single pouch. Patients using affected lots should contact their healthcare provider.
Product
FENTANYL SYSTEM — FENTANYL SYSTEM (FENTANYL)
Category
Drug
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
SevereFDA (Devices)·Z-1150-2025·2025-02-26
Philips Allura Xper FD20/20 Imaging Table Mattress Recall
Philips is recalling 114 units of the Allura Xper FD20/20 imaging table due to mattress defects that could cause patients to fall. 33 units are in the US; 81 are internationally distributed.
Product
Allura Xper FD20/20; Catalog numbers: 722038
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 (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-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-1154-2025·2025-02-26
Philips Azurion 3 M15 Patient Tables Recalled for Patient Fall Risk
Philips recalls Azurion 3 M15 imaging tables due to mattress defects that could cause patients to fall from the examination table.
Product
Azurion 3 M15; Catalog numbers: (1) 722064, (2) 722222 (3) 722280(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
HighFDA (Devices)·Z-1200-2025·2025-02-26
Medical Diagnostic Culture Media Recalled for Listeria Contamination
Remel, Inc recalls blood agar culture media used in diagnostic laboratories for potential Listeria monocytogenes contamination. The affected lot was distributed nationwide.
Product
remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1201-2025·2025-02-26
remel Blood Agar EMB Agar Biplate Recalled for Listeria Contamination
Remel's blood agar culture media plates (lot 213971) may contain Listeria monocytogenes contamination visible on the blood side. The affected product was distributed nationwide; users should discontinue use immediately.
Product
remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0235-2025·2025-02-26
Atomoxetine Capsules Recalled Due to Excess N-Nitroso Impurity
Glenmark Pharmaceuticals is recalling Atomoxetine capsules due to the presence of N-Nitroso Atomoxetine impurity above FDA recommended limits. The nationwide recall affects 80,160 bottles.
Product
ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0244-2025·2025-02-26
Atomoxetine Prescription Capsules Recalled for Impurity Above FDA Recommended Level
Glenmark Pharmaceuticals is recalling 58,368 bottles of Atomoxetine Capsules 100 mg due to N-Nitroso Atomoxetine impurity above FDA-recommended limits. The recall affects bottles distributed nationwide.
Product
ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
Category
Drug
Distribution
Distributed nationwide