State

US Virgin Islands product recalls

72,984 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 30
Most recent: 2026-09-09

Of the 177 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7676–7700 of 73161

HighFDA (Devices)·Z-1096-2025·2025-02-12
FDA Recalls PROLENE Polypropylene Sutures for Defective Packaging Seals
Ethicon is recalling PROLENE polypropylene sutures because some packages have open seals due to a manufacturing defect. Defective seals may allow pathogens to contaminate the sterile sutures, potentially causing infection.
Product
PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurosurgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V082000·2025-02-12
Volkswagen Tiguan camera control units may error at vehicle startup
Volkswagen is recalling certain Tiguan, Arteon and Audi Q3 vehicles because a camera control unit error at startup may prevent the rearview image displaying.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI TIGUAN, ARTEON, Q3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0501-2025·2025-02-12
FGF LLC Recalls Just Baked Coffee Rolls Over Listeria Contamination Risk
FGF LLC is recalling 2,017,614 cases of Just Baked Coffee Rolls (78 x 3oz packages) due to potential Listeria monocytogenes contamination. The affected product was produced on or before 12/13/24 and distributed nationwide in the US and Canada.
Product
item 8201864 JUST BAKED COFFEE ROLLS 78x3OZ, NET WT 14.62 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1088-2025·2025-02-12
Philips Azurion Patient Tables Recalled for Finger Entrapment Risk
Philips Azurion patient tables used in medical imaging systems can trap fingers between the tabletop and rails during manual repositioning, potentially causing finger injury to operators and service personnel.
Product
Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0485-2025·2025-02-12
Apple-Filled Paczki from FGF, LLC recalled for potential Listeria contamination
FGF, LLC is recalling apple-filled paczki sold nationwide due to potential contamination with Listeria monocytogenes. Affected units were produced on or before December 13, 2024.
Product
item 8201817 APPLE FILLED PACZKI 66x4 OZ, NET WT 14.85 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1079-2025·2025-02-12
Philips Allura patient tables recall due to finger entrapment risk
Philips recalls AD7 and AD7X patient tables in Allura and Azurion systems due to finger entrapment risk during manual repositioning. Operators and service personnel could suffer finger injuries.
Product
Allura Xper FD10C System Code: (1) 722001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1078-2025·2025-02-12
Philips AlluraXper Patient Tables Pose Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion fluoroscopy systems. Manual repositioning can trap fingers between the tabletop and rails, risking injury to operators and service personnel.
Product
AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1111-2025·2025-02-12
Temporary Titanium Abutments May Fracture in Dental Implants
DDS Lab temporary titanium abutments may have been installed in some dental implant restoration cases instead of definitive abutments. The components may fracture, risking restoration loosening, oral tissue injury, and aspiration.
Product
Temporary Titanium Abutments
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1091-2025·2025-02-12
Philips Azurion and Allura System Patient Tables: Finger Entrapment Risk
Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.
Product
Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1097-2025·2025-02-12
PERMA-HAND Silk Sutures Recalled for Packaging Sterility Breach
Ethicon is recalling PERMA-HAND Silk Sutures that may have open seals on packaging due to manufacturing defects, risking sterility compromise and patient infection. Approximately 78,792 units were distributed nationwide and internationally.
Product
PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H; Perma-hand Silk Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic and neurosurgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1095-2025·2025-02-12
Hologic Rapid fFN Specimen Collection Tubes May Contain Incorrect Extraction Buffer Volumes
Hologic Rapid fFN Specimen Collection Tubes from three lots may contain incorrect amounts of extraction buffer, potentially causing invalid test results or diagnostic errors in preterm delivery assessment.
Product
The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN: 71738-001). The Collection Tube (PN: 71550-001) is manufactured by a third-party supplier, MML Diagnostics Packaging, and includes the transport tube, cap, and extr
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2025·2025-02-12
Endodontic Files Recalled for Excess Irradiation Causing Package Integrity Issues
US Endodontics is recalling endodontic files due to irradiation above specification, which may compromise package integrity. The recall affects 789,729 devices distributed in the US and internationally.
Product
Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK AP120253PK AP120313PK AP125213PK AP125253PK AP125313PK AP135213PK AP135253PK AP135313PK AP145213PK AP145253PK AP145313PK AP1GP213PK AP1GP253PK AP1GP313PK O.U.S. Products: EdgeFile X7 REF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1045-2025·2025-02-12
GE Discovery XR656 HD X-ray system AEC control malfunctions during imaging
GE Medical Systems is recalling the Discovery XR656 HD X-ray imaging system due to a malfunction in the Automatic Exposure Control (AEC) feature. The defect allows continued X-ray exposure beyond intended limits without requiring operator acknowledgment.
Product
Discovery XR656 HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2025·2025-02-12
Philips Azurion and Allura Patient Tables: Finger Entrapment Hazard
Philips patient tables on Azurion and Allura imaging systems can trap fingers between the tabletop and rails during manual repositioning. Operators and service personnel are at risk of finger injury.
Product
Azurion 3 M12 System Code: (1) 722063 (2) 722221
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1044-2025·2025-02-12
Medical X-Ray System Permits Bypass of Radiation Exposure Control
GE Medical Systems' Discovery XR656HD X-Ray imaging systems can allow radiation exposures to exceed the Automatic Exposure Control limit without blocking further exposure. Approximately 3,149 units are affected worldwide, including 1,697 in the United States.
Product
Discovery XR656HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1092-2025·2025-02-12
Philips Azurion patient tables recalled for finger entrapment hazard
Philips is recalling Azurion 7 B20 patient tables due to a finger entrapment hazard between the tabletop and guiding rails during manual repositioning. Operators and service personnel could suffer finger injury.
Product
Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1081-2025·2025-02-12
Philips AlluraXper FD20 Biplane Patient Table Finger Entrapment Risk
Philips AlluraXper FD20 Biplane patient tables may cause finger entrapment between the tabletop and guiding rails during manual repositioning, affecting operators and service personnel.
Product
AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0513-2025·2025-02-12
FGF Persian Yeast Donuts Recalled Nationwide for Potential Listeria Contamination
FGF, LLC is recalling Persian yeast donuts due to potential Listeria monocytogenes contamination. The recall affects all product produced on or before December 13, 2024.
Product
item 8201884 PERSIAN YST DONUT PFD 46x3.5 OZ, NET WT 9.06 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0518-2025·2025-02-12
Just Baked Blueberry Cake Ring Recalled for Potential Listeria Contamination
FGF, LLC is recalling Just Baked Blueberry Cake Ring products for potential Listeria monocytogenes contamination. Approximately 2.0 million cases distributed nationwide to the US and Canada with production dates on or before December 13, 2024.
Product
item 8201905 JUST BAKED BLUEBERRY CAKE RING NATURALLY AND ARTIFICIALLY FLAVORED 135x2.5OZ, NET WT 21.09 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0499-2025·2025-02-12
FGF Sour Cream Cake Donuts Recalled Due to Listeria Contamination Risk
FGF's Just Baked Sour Cream Cake Donuts are being recalled nationwide due to potential Listeria monocytogenes contamination. Approximately 2 million cases produced on or before December 13, 2024 are affected.
Product
item 8201860 JUST BAKED SOUR CREAM CAKE DONUTS 120x2.5 OZ, NET WT 18.75 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0478-2025·2025-02-12
Fluff Bars Recalled Due to Potential Listeria Monocytogenes Contamination
FGF, LLC is recalling item 8201810 Fluff Bars distributed nationwide to the US and Canada due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
item 8201810 FLUFF BAR 78x2.75 OZ, NET WT 12.07 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0472-2025·2025-02-12
FGF Yeast Ring Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of yeast ring donuts nationwide due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024.
Product
item 8201804 Yeast Ring Donut 108x2.15OZ, NET WT 13.06 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0522-2025·2025-02-12
French Cruller Recall Due to Listeria Contamination Risk
FGF, LLC is recalling French Crullers (item 8201921) distributed nationwide in the US and Canada due to potential Listeria monocytogenes contamination.
Product
item 8201921 FRENCH CRULLER PFD 72x1.6 OZ, NET WT 6.48 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0511-2025·2025-02-12
French Crullers Recalled for Potential Listeria Contamination
FGF, LLC is recalling JUST BAKED FRENCH CRULLERS nationwide due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
item 8201882 JUST BAKED FRENCH CRULLERS 96x1.6 OZ, NET WT 9.60 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1102-2025·2025-02-12
ECG cable shipped with incomplete cleaning and disinfection instructions
Physio-Control is recalling 245 LIFEPAK 35 ECG cables (Lot 0224) because the shipped instructions do not include proper cleaning and disinfection procedures, creating potential cross-contamination risks.
Product
LIFEPAK 35 ECG cable REF 11111-000041
Category
Medical Device
Distribution
Distributed nationwide