State

US Virgin Islands product recalls

73,495 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: 39
Most recent: 2026-10-14

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 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24276–24300 of 73672

HighFDA (Devices)·Z-2036-2021·2021-07-14
Cesarean Birth Drapes recalled due to defective plastic film causing sticking
Cardinal Health is recalling Cesarean Birth Drapes due to a plastic film defect. The defect causes the drapes to stick, preventing proper unfolding and application during surgery.
Product
Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen, Catalog Number 29442N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2033-2021·2021-07-14
Sterile Angiography Drapes Recalled Due to Sticking Plastic Film Defect
Cardinal Health is recalling 3,192 units of Sterile Radial/Femoral Angiography Drapes due to sticking plastic film that may prevent proper unfolding and application during surgical procedures.
Product
Sterile Radial/Femoral Angiography Drape, Catalog Number 29529 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2028-2021·2021-07-14
Atellica analyzer valves recalled for manufacturing defect affecting diagnostic accuracy
Siemens recalls Atellica analyzers (CH 930, IM 1300, IM 1600) due to valve manufacturing defects that may cause leaking and affect clinical test result accuracy.
Product
Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic testing of clinical specimens SMN 11066000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2013-2021·2021-07-14
Randox RX Imola Analyzer Software Freeze Recall - 50 Units Affected
Randox recalls 50 RX Imola Analyser units nationwide and in Puerto Rico due to software freezing that prevents test results from displaying.
Product
Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2004-2021·2021-07-14
GE Healthcare Revolution CT collimator blade malfunction causing radiation dose variance
GE Healthcare is recalling Revolution CT systems where a collimator blade malfunction may cause x-ray radiation doses to be delivered in amounts larger or smaller than prescribed.
Product
Revolution CT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2032-2021·2021-07-14
Nonsterile Femoral Angiography Drapes Recalled Due to Sticking Plastic Film Defect
Cardinal Health is recalling 26,250 units of Nonsterile Femoral Angiography Drapes due to a manufacturing defect causing the drapes to stick and preventing proper application. This may compromise surgical site protection.
Product
Nonsterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525N - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2038-2021·2021-07-14
Angiography and Cesarean Birth Drapes recalled due to sticking defect
Cardinal Health is recalling Nonsterile Femoral Angiography and Cesarean Birth Drapes (15,360 units) because plastic film causes sticking that may prevent proper unfolding and application.
Product
Nonsterile Femoral Angiography Drape, Catalog Numbers: a) 29460NB, b) 29456NB - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0651-2021·2021-07-14
Xylocaine Lidocaine Injection Recalled for Low Epinephrine Assay Results
Fresenius Kabi USA LLC is recalling Xylocaine-MPF with Epinephrine 1:200,000 injection vials nationwide due to low out-of-specification results for epinephrine assay.
Product
XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·21163·2021-07-14
Academy Sports Ozone 500 24-Inch Bicycles Recalled for Fall Hazard
Academy Sports + Outdoors is recalling about 3,860 Ozone 500 Girls' and Boys' Elevate 24-Inch Bicycles because the rear shock spring can become stuck, creating a pinch point and posing a fall hazard to riders.
Product
Ozone 500® Girls' and Boys' Elevate 24-Inch Bicycles
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2031-2021·2021-07-14
Sterile Femoral Angiography Drape Sticks; Cannot Unfold Properly
Cardinal Health is recalling 574 units of Sterile Femoral Angiography Drapes because the plastic film causes the drapes to stick, preventing proper unfolding and application during surgery.
Product
Sterile Femoral Angiography Drape with Single Pouch, Catalog Number 29525 - Product Usage: intended to be used as protective patient coverings, such as to isolate the site of a surgical incision from microbial and other contamination.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0650-2021·2021-07-14
Genentech Xolair Injection Recalled for Failed Stability Specifications
Genentech is recalling two lots of Xolair (omalizumab) injection nationwide due to out-of-specification Polysorbate 20 content detected at the 12-month stability testing timepoint. The affected lots are 3352758 and 3352759, both with August 2021 expiration dates.
Product
XOLAIR — XOLAIR (OMALIZUMAB)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0786-2021·2021-07-14
Hatch Verde Salsa Recalled for Potential Foreign Material
Heritage Family Specialty Foods, Inc. is recalling Hatch Verde Salsa Medium (12 oz jars) due to potential foreign material contamination. The recall affects 646 cases distributed nationwide.
Product
Hatch Verde Salsa Medium Net Wt. 12 oz (340g) 6 jars per case packaged in clamshell container UPC Code: 810041591999
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0787-2021·2021-07-14
Taco Casa Green Salsa Recalled for Potential Foreign Material
Heritage Family Specialty Foods is recalling Taco Casa Green Salsa due to potential foreign material contamination. The affected product was distributed nationwide.
Product
E6164J2 Taco Casa Green Salsa 8 x 4 lb (1.8 kg) pouches
Category
Food
Distribution
Distributed nationwide
ModerateCPSC·21164·2021-07-14
Walgreens Recalls Disney Baby Winnie the Pooh Rattle Sets for Choking Hazard
Walgreens is recalling about 54,000 Disney Baby Winnie the Pooh Rattle Sets because the feet can detach and pose a choking hazard to young children. Consumers should immediately remove the rattle from children and contact Walgreens for a refund.
Product
Disney Baby Winnie the Pooh Rattle Sets
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2012-2021·2021-07-14
ACE Control Set stability claim failure requires updated handling instructions
Sentinel CH SpA is recalling ACE Control Set diagnostic control kits due to stability claims after reconstitution that do not meet specified requirements. Updated handling instructions have been provided to affected users.
Product
ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V529000·2021-07-13
Entegra and Jayco recreational vehicles recalled for window adhesive failure
Jayco is recalling certain 2019-2021 recreational vehicles with Hehr 6400 series windows due to adhesive failure. The window vent may detach, increasing the risk of crash or injury.
Product
ENTEGRA — ENTEGRA, JAYCO INSIGNIA, REATTA, ANTHEM, ASPIRE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E063000·2021-07-13
Cummins Recalls L9 Diesel Engines Due to Fuel Hose Leak Risk
Cummins is recalling specific L9 Diesel Engines equipped with remote Stage 2 fuel filters because a fuel leak may occur from the hose between the fuel pump and filter head.
Product
FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V530000·2021-07-13
Micro Bird Recalls School Buses Due to Emergency Door Defect
Micro Bird is recalling 2003-2022 school buses because the service door emergency release handle may bind, preventing evacuation in an emergency.
Product
MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, G5 SCHOOL BUS, T-SERIES SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V531000·2021-07-13
Micro Bird Transit Buses Recalled for Service Door Emergency Release Defect
Micro Bird is recalling 1,323 transit buses because the service door emergency release handle may bind, preventing evacuation in an emergency.
Product
MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, MB II TRANSIT BUS, T-SERIES TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V528000·2021-07-13
Summit Bodyworks Recalls 2017 Freightliner M2 for Excessively Bright Rear Lights
Summit Bodyworks is recalling one 2017 Freightliner M2-106 because its rear LED lights are too bright, potentially blinding other drivers and increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER M2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V526000·2021-07-12
Mercedes-Benz Recalls 2020 GLB 250 for Electrical Fire Risk
Mercedes-Benz is recalling 2020 GLB 250 vehicles because an incorrect voltage converter socket may cause excessive voltage in the second-row power outlet, increasing fire risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLB 250
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V527000·2021-07-12
2021 Mercedes-Benz side crash sensor connector defect affects airbag deployment
Mercedes-Benz is recalling certain 2020-2021 models because side crash sensor connectors may come loose, delaying airbag and seatbelt activation during side impact crashes. Dealers will inspect and replace sensors at no cost.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63, G 550, AMG G63, E 450
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V523000·2021-07-09
Recreational vehicles recalled for defective window adhesive on multiple models
Forest River and Coachmen recreational vehicles with Hehr 6400 Series windows are being recalled due to adhesive failure that may cause window vents to detach. Detachment increases the risk of crashes and injuries.
Product
FOREST RIVER — FOREST RIVER, COACHMEN CEDAR CREEK, GEORGETOWN, SPORTSCOACH, MIRADA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V524000·2021-07-09
Hyundai Santa Fe and Sonata recalled for fuel pipe leak fire risk
Fuel may leak at a pipe connection in affected 2021-2022 Hyundai Santa Fe and Sonata vehicles with 2.5L engines, increasing fire risk.
Product
HYUNDAI — HYUNDAI SONATA, SANTA FE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V525000·2021-07-09
2021 Nissan Rogue Sport Liftgate Hinges May Separate in Rear Crashes
Nissan is recalling 2021 Rogue Sport vehicles because liftgate hinges may separate during rear-end crashes, compromising door retention. Dealers will replace the hinges free of charge.
Product
NISSAN — NISSAN redundant ROGUE SPORT
Category
Vehicle
Distribution
Distributed nationwide