State

US Virgin Islands product recalls

73,809 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

Of the 178 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 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47226–47250 of 73987

SevereFDA (Devices)·Z-2401-2016·2016-08-17
Invacare Bariatric Bed Foot Section Recalled for Fire Hazard
Invacare Corporation is recalling 3,050 Bariatric Bed Foot Sections because a junction box defect may cause sparks and fire.
Product
Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V605000·2016-08-17
Road Rescue Emergency Vehicles Recalled for Electrical Short Circuit Risk
REV is recalling 2010-2016 Road Rescue emergency vehicles due to power control modules that may cause short circuits, risking electrical damage, loss of headlights, or fire.
Product
ROAD RESCUE — ROAD RESCUE DURAMEDIC, ULTRAMEDIC, TRANSMEDIC, SPECIALTY VEHICLE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1895-2016·2016-08-17
Let's Do Lunch Recalls Italian Deli Flatz for Listeria Risk
Let's Do Lunch, Inc. is recalling Cafe Favorites Italian Deli Flatz due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.
Product
Cafe Favorites Italian Deli Flatz Code #C22548/22548
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2399-2016·2016-08-17
Invacare Bariatric Bed Recalled for Junction Box Fire Risk
Invacare is recalling 2,184 Bariatric Beds because a defect in the Junction Box may cause sparks, posing a fire hazard in the presence of flammable materials.
Product
Invacare¿ Bariatric Bed w/o mattress & rails, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2400-2016·2016-08-17
Invacare Bariatric Bed Recalled for Potential Fire Hazard from Junction Box Sparks
Invacare is recalling 2,702 Bariatric Beds because the junction box may spark, posing a fire risk in the presence of flammable materials.
Product
Invacare¿ Bariatric Bed with mattress and rails , Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2388-2016·2016-08-17
Edan Diagnostics Recalls EtCO2 Modules for Incorrect CO2 Readings
Edan Diagnostics is recalling 521 EtCO2 modules used in patient monitors because they may provide incorrect CO2 readings.
Product
EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80, iM50, M50, iM70, iM60, iM8, iM8A, iM8B Patient Monitors and iM60 Vet, iM70 Vet Veterinary Monitors EtCO2 module is an optional component of the following machines: iM80, iM50, M50, iM70, iM60 and iM8, iM8A, iM8B, iM60…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2379-2016·2016-08-17
Merge PACS software recalled due to patient name mismatch
Merge Healthcare is recalling PACS software versions V6.0.2.0 MR2 and earlier because patient names in the interface do not match the displayed images.
Product
Merge PACS software. Product was distributed under the AMICAS label, Brighton, MA, but labeling was later changed to Merge Healthcare, Hartland, WI.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2397-2016·2016-08-17
Zimmer Biomet Recalls Zyston Transform Instrument Cases Due to Locking Defect
Zimmer Biomet Spine, Inc. is voluntarily recalling Zyston Transform Instrument Cases and Implant Kits because the implant locking mechanism is not functioning as intended.
Product
Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2374-2016·2016-08-17
Teleflex Servo Humidifier 163 Recalled Due to Connector Cracks
Teleflex Medical is recalling Servo Humidifier 163 units because cracks may occur at the ISO female connectors.
Product
Servo Humidifier 163, Model 01-06-8125-8, REF 6419365 Product Usage: A heat and moisture condenser (artifical nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2376-2016·2016-08-17
Hill-Rom Recalls Volker Series Hospital Beds Due to Side Rail Defect
Hill-Rom is recalling Volker 2080, 2082, S 280, and S 282 series hospital beds because the side rail latch may fail, causing the rail to lower and the patient to fall.
Product
Volker 2080, 2082, S 280 and S 282 series beds with lateral release button. A/C Powered Adjustable Hospital Bed Product Usage: Volker model 2080/3010/3080 nursing beds are intended for the care of residents in rooms in nursing homes, in residential homes for the elderly and…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16245·2016-08-17
Xenith Recalls Football Helmets Due to Shell Cracking Hazard
Xenith is recalling specific football helmets because the shells can crack, posing a risk of head injuries. No injuries have been reported.
Product
Football helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2396-2016·2016-08-17
Stryker Recalls Exeter Rasp Handle Due to Malfunctioning
Stryker Howmedica Osteonics Corp. is recalling 241 Exeter Rasp Handles because they may malfunction during use.
Product
Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a reusable instrument which is part of the Exeter femoral hip system. Exeter femoral rasps are assembled with the rasp handle and locked in place by closing down the lever on the rasp handle. The rasp handle…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2398-2016·2016-08-17
Zimmer Biomet Recalls Zyston Transform Implant Kits Due to Locking Defect
Zimmer Biomet Spine is recalling five Zyston Transform Implant Kits because the locking mechanism is not functioning as intended.
Product
Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2353-2016·2016-08-17
Stryker S3 MedSurg Bed Fowler Control Failure Recall
Stryker is recalling S3 MedSurg Beds because CPU board failures can cause the backrest electronic controls to stop working.
Product
S3 MedSurg Bed, Model 3005. Stryker Medical
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2016·2016-08-17
Ortho VITROS Estradiol Reagent Recall Due to Fulvestrant Cross-Reactivity
Ortho Clinical Diagnostics is recalling VITROS Estradiol Reagent Packs because the drug Fulvestrant causes falsely high test results in postmenopausal women.
Product
VITROS Immunodiagnostic Products Estradiol Reagent Pack, Unique Device Identifier No. 10758750005017, REF/Catalog Number/Product Code 855 2630; IVD -- Ortho-Clinical Diagnostics, Pencoed, Bridgend CF35 5PZ, UK --- The VITROS Estradiol test is performed using the VITROS Estradiol…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2390-2016·2016-08-17
Stryker Triathlon Tibial Alignment Handle Recalled Due to Weld Defect
Stryker Howmedica Osteonics is recalling 47 units of the Specialty Triathlon Tibial Alignment Handle because the secondary locking mechanism may disassociate during surgery due to a weld defect.
Product
Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with Secondary Lock, Non-Sterile, Used to complement or replace the standard instruments used during the implantation of hip, knee, trauma and upper extremities implants
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2377-2016·2016-08-17
Stryker Recalls Triathlon Modular Handle Instruments Due to Fit Issues
Stryker Howmedica Osteonics is voluntarily recalling Triathlon Modular Handle instruments because press fit specifications were not met, potentially causing disassociation.
Product
Stryker Orthopaedics Modular Handle Triathlon Instruments, Non-Sterile, REF 6541-4-808, Lot 123, NDC M546654148080S Product Usage: Is a reusable instrument that is part of the Triathlon Primary total knee arthroplasty (TKA) system as well as the Triathlon Partial Knee…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2344-2016·2016-08-17
Siemens Artis Angiography Systems Recalled for Image Reproduction Failure
Siemens Medical Solutions is recalling 51 Artis zee and Artis Q angiography systems due to a software error that may cause image loss after startup.
Product
Artis zee/ zeego, Artis Q/ Q.zen, stand alone system, software controlled Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959, 10848281, 10848282, 10848283, 10848353, 10848255 Artis zee / zeego and Q/ Q.zen is a family of dedicated angiography systems developed for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2394-2016·2016-08-17
Siemens AXIOM Artis X-Ray Systems Recalled for Cooling System Contamination
Siemens is recalling AXIOM Artis angiography systems because biomass contaminants in the cooling system may damage the pump.
Product
ARTIS ZEE AND ZEEGO, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2405-2016·2016-08-17
Topcon Recalls PASCAL Synthesis Ophthalmic Laser Systems Due to Titration Anomaly
Topcon Medical Laser Systems is recalling 205 PASCAL Synthesis ophthalmic laser systems worldwide due to a software anomaly affecting the titration process when specific functions are used.
Product
Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The system can perform single shot photocoagulation as is performed conventionally.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2395-2016·2016-08-17
Siemens Medical Solutions Recalls Artis Q and Q.Zen Angiography Systems
Siemens Medical Solutions is recalling Artis Q and Q.Zen angiography systems because biomass in the cooling system may damage the pump.
Product
ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM, interventional fluoroscopic x-ray system22 AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2375-2016·2016-08-17
Nobel Biocare Recalls Guided Surgery Kit Instructions for Incorrect Drill Protocol
Nobel Biocare is recalling 231 Guided Surgery Kits because the Instructions for Use contain an incorrect drill protocol. The kits are used for NobelParallel CC Implants.
Product
Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Kit Instructions for Use (IFU): "NobelGuide for NobelParallel Conical Connection", id # 2002 and Manual: Guided Surgery with NobelParallel Conical Connection", id # 79423. Article # 38072, Nobel Parallel CC Guided…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2393-2016·2016-08-17
Siemens AXIOM Artis Angiography Systems Recalled for Cooling System Contamination
Siemens is recalling AXIOM Artis angiography systems because biomass contamination in the cooling system may damage the pump.
Product
AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2378-2016·2016-08-17
BD Tritest CD3/CD4/CD45 Reagent Recalled for Incorrect Labeling
Becton, Dickinson and Company is recalling 14,089 vials of BD Tritest CD3 FITC/CD4 PE/CD45 PerCP because the label incorrectly states the product contains gelatin.
Product
BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP with Gelatin and 0.1% sodium azide. Hematology: BD Tritest CD3 fluorescein isothiocyanate (FITC)/CD4 phycoerythrin (PE)/CD45 peridinin chlorophyll…
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·16767·2016-08-16
Sauder Woodworking Recalls Storybook Four-Drawer Chests for Tip-Over Hazard
Sauder Woodworking is recalling about 8,000 Storybook four-drawer chests sold at Walmart.com due to a serious tip-over hazard that could injure children.
Product
Four-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide