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.

7701–7725 of 73161

HighFDA (Drugs)·D-0219-2025·2025-02-12
Hydralazine Hydrochloride Tablets Recalled Due to Impurities and Degradation
SKY Packaging recalls Hydralazine Hydrochloride 25 mg tablets nationwide due to failed quality specifications for impurities and degradation.
Product
HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0523-2025·2025-02-12
Flavored Raspberry Bismark Pastries Recalled for Potential Listeria Contamination
FGF, LLC is recalling flavored raspberry Bismark pastries over potential contamination with Listeria monocytogenes. The recall affects product produced on or before December 13, 2024.
Product
item 8201922 FLAVORED RASPBERRY BISMARK PFD 3OZ, NET WT 13.16 LB
Category
Food
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 (Food)·F-0516-2025·2025-02-12
Apple Cider Cake Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling Just Baked Apple Cider Cake Rings due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed nationwide in the US and Canada.
Product
item 8201901 JUST BAKED APPLE CIDER CAKE RINGS WITH NATURAL FLAVORS 144x2.5OZ, NET WT 22.5 LB
Category
Food
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-1090-2025·2025-02-12
Philips Azurion 5 M20 Patient Tables Recalled for Finger Entrapment Hazard
Philips Azurion 5 M20 x-ray system patient tables can trap fingers between the tabletop and guiding rails during repositioning. The hazard may cause finger injury to operators and service personnel.
Product
Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1083-2025·2025-02-12
Philips AlluraXper Operating Room Table Finger Entrapment Hazard
The Philips AlluraXper FD20 operating room table can trap fingers between the guiding rails and tabletop during manual repositioning, potentially injuring operators and service personnel.
Product
AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035
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
HighNHTSA·25V081000·2025-02-12
Volkswagen Atlas transmissions may have been manufactured incorrectly
Volkswagen is recalling certain 2025 Atlas and Atlas Cross Sport vehicles because the transmission may have been manufactured incorrectly, which can result in a loss of drive power.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1077-2025·2025-02-12
Philips AD7 and AD7X patient tables recalled due to finger entrapment risk
Philips has recalled the AD7 and AD7X patient tables used in medical imaging systems because fingers can become entrapped between the tabletop and guiding rails during manual repositioning, potentially causing injury.
Product
Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0476-2025·2025-02-12
FGF LLC Persian Donut Recalled for Potential Listeria Contamination
FGF LLC is recalling Persian Donut item 8201808 nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard it or return it to the retailer.
Product
item 8201808 PERSIAN DONUT 78x2.25 OZ, NET WT 9.87 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2025·2025-02-12
Belmont Medical 3-Spike Disposable Set May Leak During Use
The Belmont Medical 3-Spike Disposable Set may leak during priming due to a crack in its female quick connector, potentially delaying warmed infusions in hospital settings.
Product
Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser RI-2. Designed to be used in general operation in hospital or alternate care environments to provide warmed blood and fluids to any patients e10 kg requiring warmed infusion. Part Number:903-00006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1093-2025·2025-02-12
Philips Azurion patient tables recalled for finger entrapment risk
Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.
Product
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
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 (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 (Devices)·Z-1105-2025·2025-02-12
NeiMed NasoGel nasal spray recalled due to stability failure
Neilmed Pharmaceuticals is recalling NasoGel for Dry Noses due to stability failure that may allow microbial growth. The product was distributed across 30 U.S. states and to five countries.
Product
NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL GSP30-SWE-INTL GSP30-ENG-INT GSP30-MAL-INTL GSP30-SPA-INT NasoGel Spray is a saline-based gel formula that can be sprayed to moisturize and lubricate dry and i
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 (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-1094-2025·2025-02-12
Philips Azurion and Allura Patient Table Finger Entrapment Risk
Philips Azurion 7 M20 and Allura patient tables pose a finger entrapment risk during manual repositioning. Fingers can get caught between the tabletop and guiding rails, potentially causing finger injury to operators and service personnel.
Product
Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233
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-1101-2025·2025-02-12
Dental implants recalled for manufacturing defect affecting sterile packaging
Nobel Biocare recalled N1 TiUltra TCC dental implants due to a manufacturing defect that may puncture the sterile blister packaging. The defect is a sharp pin created during injection molding that could compromise product sterility.
Product
. Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP 4.0x11mm . Nobel Biocare N1 TiUltra TCC RP 4.0x13mm Nobel Biocare N1 TiUltra TCC implants are intended for use as an endosseous dental implant in the maxilla or mandible for anchoring or supporting
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-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
HighNHTSA·25V080000·2025-02-12
Audi Q5 and A7 high voltage batteries may overheat
Volkswagen is recalling certain 2021-2024 Audi Q5 and 2022 A7 e plug-in hybrid vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7 E
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V079000·2025-02-12
Porsche Recalls 2025 911 Models Due to Headlight Glare Software Error
Porsche is recalling 878 2025 911 vehicles because a software error causes low beam headlights to create excessive glare for oncoming traffic, increasing crash risk.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide