State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37926–37950 of 73916

SevereFDA (Drugs)·D-0911-2018·2018-07-11
Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error
Fagron Compounding Services is recalling 390 prefilled syringes of Neostigmine Methylsulfate Injection Solution because some may be incorrectly labeled with the wrong strength.
Product
Neostigmine Methylsulfate Injection Solution, 3 mg per 3 mL, 1 mg per mL, 3 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0910-2018·2018-07-11
Fagron Recalls Neostigmine Methylsulfate Syringes Due to Labeling Error
Fagron Sterile Services is recalling 840 prefilled syringes of Neostigmine Methylsulfate Injection Solution because they may be incorrectly labeled with the wrong strength.
Product
Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2293-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V463000·2018-07-11
Pierce Emergency Vehicles Recalled for Aerial Bracket Detachment Risk
Pierce is recalling 2007-2017 emergency vehicles because an aerial device bracket may detach and fall, potentially striking a person below.
Product
PIERCE — PIERCE ARROW XT, QUANTUM, IMPEL, VELOCITY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0890-2018·2018-07-11
Ingenus Recalls Irinotecan Hydrochloride Injection Due to Potency Issues
Ingenus Pharmaceuticals is recalling specific lots of Irinotecan Hydrochloride Injection because they had high out-of-specification assay values for potency.
Product
IRINOTECAN HYDROCHLORIDE — IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V461000·2018-07-11
Lamborghini Recalls 2015-2016 Aventador Models for Wheel Detachment Risk
Lamborghini is recalling 2015-2016 Aventador SV vehicles because loose brake disc bolts may cause wheels to detach, increasing crash risk.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR, AVENTADOR ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2342-2018·2018-07-11
Beaver Visitec Safety Sideport Knife Blades May Detach During Surgery
Beaver Visitec is recalling Safety Sideport Knives because blades may fall out of handles due to non-cured epoxy. The defect poses a risk during ophthalmic surgery.
Product
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V464000·2018-07-11
Volkswagen Recalls 2015-2018 Golf Models for Ignition Key Removal Defect
Volkswagen is recalling 2015-2018 Golf and Golf Sportwagen vehicles because silicate buildup may allow the key to be removed while the car is not in Park, increasing rollaway risk.
Product
VOLKSWAGEN — VOLKSWAGEN GOLF, GOLF SPORTWAGEN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation Complaints
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to higher-than-expected complaints of femoral head/hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-136
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18753·2018-07-11
Burton Recalls Snowboard Boots Due to Unexpected Binding Release Hazard
Burton is recalling about 4,800 Step On snowboard boots because they can unexpectedly release from bindings, posing a fall hazard. No injuries have been reported.
Product
Snowboard boots
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2292-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, 6260-9-036
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V462000·2018-07-11
KZRV Recalls 2018-2019 Sportsmen Trailers Due to Propane Leak Risk
KZRV is recalling 2018-2019 Sportsmen recreational trailers because propane gas may leak at the outside kitchen cooktop, increasing fire risk.
Product
KZRV — KZRV SPORTSMEN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-140
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2297-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-144
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V460000·2018-07-11
Jayco Recalls 2018 Octane Travel Trailers Due to Missing Generator Exhaust Pipe
Jayco is recalling 2018 Octane travel trailers with optional generators because a missing exhaust pipe may allow exhaust to enter the trailer, increasing injury risk.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER OCTANE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-336
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2341-2018·2018-07-11
Intuitive Surgical Recalls da Vinci X Systems with Defective Arm Controller Boards
Intuitive Surgical is recalling 35 da Vinci X Surgical Systems because defective Arm Controller Joint boards have a high rate of failure.
Product
da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System (da Vinci X Surgical System Mode IS4200) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments including rigid…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V465000·2018-07-11
BMW and MINI Recall 5,309 Vehicles for Crankshaft Sensor Defect
BMW is recalling 5,309 vehicles because a crankshaft sensor firmware error may cause the engine to stall, increasing crash risk.
Product
MINI — MINI, BMW JCW, X2, COUNTRYMAN, CLUBMAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2294-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific lots of LFIT Anatomic CoCr Femoral Heads due to a higher than expected number of complaints about femoral head and hip stem disassociation.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-044
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2334-2018·2018-07-11
St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recall
St. Jude Medical is recalling 986 Confirm Rx Insertable Cardiac Monitors because exposure to sub-freezing temperatures caused a transient battery voltage drop, resulting in an incorrect low battery indicator display.
Product
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for the monitoring and diagnostic evaluation of patients who experience unexplained symptoms such as: dizziness, palpitations, chest pain, syncope, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2344-2018·2018-07-11
Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products PHYT Slides
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products PHYT Slides due to a potential for imprecise results in quality control and patient samples.
Product
VITROS Chemistry Products PHYT Slides, Catalog Number 8298671. in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2335-2018·2018-07-11
St Jude Medical Recalls Merlin PCS Programmer Software for ICM Battery Display Error
St Jude Medical is recalling Merlin PCS Programmer Software to address an incorrect low battery indicator on Confirm Rx ICM devices caused by supply chain temperature exposure.
Product
Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, and for this recall the software that resides on the programmer (software model 3330) is the method of delivery of the new…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0892-2018·2018-07-11
Qualgen Recalls Estradiol Pellets Due to Incorrect or Missing Lot and Expiration Dates
Qualgen, LLC is recalling Estradiol 20mg Pellets because the vials have incorrect or missing lot and expiration dates.
Product
ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0893-2018·2018-07-11
Qualgen Recalls Testosterone Pellets Due to Incorrect Lot and Expiration Dates
Qualgen, LLC is recalling Testosterone 200 mg Pellets because the vials have incorrect or missing lot and expiration dates.
Product
TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01
Category
Drug
Distribution
Distributed nationwide