State

US Virgin Islands product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

851–875 of 73084

SevereFDA (Devices)·Z-2672-2026·2026-07-08
GORE TAG Thoracic Branch Endoprosthesis Side Branch Component Recall
W. L. Gore & Associates is recalling 467 GORE TAG Thoracic Branch Endoprosthesis Side Branch Components worldwide due to risk of catheter separation during deployment.
Product
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes Puerto Rico) and Canada: TSB080806A, TSB081006A, TSB081206A, TSB081506A, TSB081706A, TSB121506A, TSB121706A, TSB122006A EMEA Countries, Australia, New Zealand:
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0644-2026·2026-07-08
PurPrep Povidone Iodine and Isopropyl Alcohol Applicators Recall
CareFusion 213, LLC is recalling PurPrep sterile applicators distributed nationwide because unsterilized units intended for further processing were distributed to customers outside the intended channel.
Product
PURPREP — PURPREP (POVIDONE IODINE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0646-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled for Lack of Sterility Assurance
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators because unsterilized units intended for further processing were distributed to customers outside the intended distribution channel, creating a lack of sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V441000·2026-07-08
BMW Recalls 29,119 Vehicles Due to Starter Relay Fire Risk
BMW is recalling 29,119 vehicles because a corroded starter relay may overheat and short circuit, increasing the risk of a fire.
Product
BMW — BMW 530E XDRIVE IPERFORMANCE, 740LE XDRIVE IPERFORMANCE, 530E IPERFORMANCE, 330E IPERFORMANCE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0649-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled for Lack of Sterility Assurance
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators distributed nationwide because unsterilized units intended for further processing were shipped to customers outside the intended distribution channel.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V438000·2026-07-08
BMW and Toyota vehicles recalled due to engine starter fire risk
BMW of North America, LLC is recalling various BMW and Toyota Supra models because the engine starter may overheat and catch fire.
Product
BMW — BMW, TOYOTA Z4, 430I XDRIVE, 530I XDRIVE, 330I XDRIVE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0675-2026·2026-07-08
Cinacalcet Tablets Recalled for cGMP Deviations
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride Tablets, 60 mg due to cGMP deviations involving the presence of N-nitroso-cinacalcet above acceptable daily intake levels.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2621-2026·2026-07-08
Preop Kit-NS surgical kits recalled for bacterial contamination
A M S Preop Kit-NS surgical convenience kits are being recalled due to contamination with Paenibacillus phoenicis bacteria discovered during sterilization testing. The kits were distributed nationwide in PA, GA, CA, and WA.
Product
A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V443000·2026-07-08
Husqvarna and GasGas Motorcycles Recalled for Brake Caliper Cracks
KTM North America is recalling certain 2022-2024 Husqvarna FE 501S, FE 350S, and 2024 GasGas ES 350 and ES 500 motorcycles due to a potential rear brake caliper crack that could reduce braking ability and increase crash risk.
Product
HUSQVARNA — HUSQVARNA, GASGAS FE 350S, ES 350, ES 500, FE 501S
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2670-2026·2026-07-08
Radius VSM ECG Pre-connected Set Recalled for Incorrect Heart Rate Detection
Masimo Corporation is recalling Radius VSM ECG pre-connected sets because the ECG electrode assembly may incorrectly detect extreme bradycardia or tachycardia and trigger false alarms on patients with normal heart rates, potentially distracting clinicians from true positive alarms and delaying treatment.
Product
Radius VSM ECG pre-connected Set, REF: 4842, 4695
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2637-2026·2026-07-08
CRE Wireguided 18-20mm 240cm medical devices recalled for sterile breach
Boston Scientific Corporation is recalling CRE Wireguided 18-20mm 240cm devices worldwide due to a potential sterile breach of the pouches in which the devices are packaged.
Product
CRE Wireguided 18-20mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2646-2026·2026-07-08
RayCare 2024A SP1 Oncology Information System Software Recall
RayCare 2024A SP1 oncology software may lose data if beam set delivery notes are modified simultaneously or updated during treatment sessions, with users not notified of changes.
Product
RayCare 2024A SP1. Oncology Information Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2638-2026·2026-07-08
Baxter Head Positioning Adapter May Loosen During Patient Positioning
Baxter Healthcare is recalling an Adapter for Head Positioning (Model 1739994) used on operating tables because it may become loose and unintentionally move during patient positioning.
Product
Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper Back Section H V U component (product code 1909813) on Baxter operating tables
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0661-2026·2026-07-08
Cinacalcet Tablets Recalled for N-Nitroso Impurity Exceeding Limits
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride 30 mg tablets due to the presence of N-nitroso-cinacalcet above the acceptable daily intake. The affected product was distributed nationwide.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0655-2026·2026-07-08
Prednisolone Acetate Ophthalmic Suspension Recalled for Foreign Substance
Lupin Pharmaceuticals is recalling Prednisolone Acetate Ophthalmic Suspension, USP, 1% due to the presence of a foreign substance. Affected lot numbers were distributed nationwide.
Product
PREDNISOLONE ACETATE — PREDNISOLONE ACETATE (PREDNISOLONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2647-2026·2026-07-08
RayCare 2024A SP4 Oncology System Beam Set Delivery Note Data Loss
RayCare 2024A SP4 oncology information system may lose data or fail to notify users when beam set delivery notes are modified simultaneously or updated during treatment sessions.
Product
RayCare 2024A SP4. Oncology Information Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2629-2026·2026-07-08
Boston Scientific CRE Pro Wireguided 12-15mm Esophageal Stent Recall
Boston Scientific is recalling CRE Pro Wireguided 12-15mm 240cm esophageal stents due to a potential sterile breach in the device packaging. Affected units were distributed worldwide.
Product
CRE Pro Wireguided 12-15mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2606-2026·2026-07-08
Medline Convenience Kits with Swan-Ganz Catheters Recalled
Medline Industries is recalling convenience kits containing Swan-Ganz catheters due to leaks and breakage of the proximal injectate lumen hub, which may cause infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2608-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Industries is recalling convenience kits containing Swan-Ganz catheters due to defects in the proximal injectate lumen hub that may leak or break, risking infection, medication loss, and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ARTERIAL LINE TOTE DYNJ8407
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2618-2026·2026-07-08
Medacta Short Monobloc Stem Broaches Surgical Instruments Shoulder Implant
Medacta USA is recalling Short Monobloc Stem Broaches used in shoulder replacement surgery due to positioning misalignment that may increase risk of fracture in the upper arm bone.
Product
Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.0977, 15/04.01.10.0978, 16/04.01.10.0979 Part of Medacta Shoulder System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2628-2026·2026-07-08
CRE Pro Wireguided medical device sterile packaging breach recall
Boston Scientific Corporation is recalling the CRE Pro Wireguided 10-12mm 240cm device due to potential sterile breach of the pouches in which devices are packaged. The affected product has been distributed worldwide.
Product
CRE Pro Wireguided 10-12mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2611-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters Nationwide
Medline is recalling convenience kits containing Swan-Ganz catheters with a defective proximal injectate lumen hub that may leak, break, or cause infection and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH CDS982523M
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V439000·2026-07-08
Forest River Recalls 2026-2027 Salem and Wildwood Travel Trailers for Incorrect Weight Label
Forest River is recalling 2026-2027 Salem and Wildwood travel trailers because the Federal Placard may display an incorrect Gross Vehicle Weight Rating, potentially leading to overloading.
Product
FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2609-2026·2026-07-08
Medline Convenience Kits Containing Recalled Swan-Ganz Catheters
Medline is recalling convenience kits containing Swan-Ganz catheters due to leaks and breakage of the proximal injectate lumen hub, which may cause infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED RN CDS DYNJ905936B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0660-2026·2026-07-08
Amphetamine extended-release capsules contain immediate-release pellets after label mix-up
Mixed amphetamine salts extended-release capsules, 5 mg, from Lannett are being recalled because the capsules contain only immediate-release pellets. 1,392 bottles affected.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SULFATE, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE SULFATE AND AMPHETAMINE ASPARTATE)
Category
Drug
Distribution
Distributed nationwide