State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57701–57725 of 74005

HighFDA (Devices)·Z-2115-2014·2014-07-30
Heartsine AED Electrode Pouches Recalled for Difficulty Opening
Heartsine is recalling Pad-Pak and Pedi-Pak electrode accessories for the Samaritan PAD 300P and 350P because some sealed foil pouches are difficult to open, potentially delaying therapy.
Product
Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P and 350P device (SAM 300P and 350P). Automated External Defibrillator electrode supplies. The Pedi-Pak is specifically designed for use with the HeartSine Samaritan PAD 300P and 350P device. It contains…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2100-2014·2014-07-30
Terumo Recalls Sarns Two-stage Venous Return Cannulae Due to Particulate
Terumo CVS is recalling Sarns Two-stage Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with 1/2" & 3/8" flare or connector Product Usage: The Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14C005000·2014-07-30
Recaro Recalls ProRIDE and Performance RIDE Child Restraints for Tether Defect
Recaro is recalling specific ProRIDE and Performance RIDE child restraints because the top tether anchorage may detach in a crash, increasing injury risk.
Product
CHILD SEAT:TETHER: CONNECTOR/CLIP recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2114-2014·2014-07-30
GE Healthcare Recalls CARESCAPE Monitor B650 Due to Sound Loss
GE Healthcare is recalling CARESCAPE Monitor B650 units because they may lose alarm sounds when an external display is connected via a USB extender with an active hub.
Product
GE Healthcare, CARESCAPE Monitor B650. A multi-parameter patient monitor intended for use in multiple areas and intrahospital transport within a professional healthcare facility.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V563000·2014-07-30
Honda Recalls 2015 Fit Vehicles Due to Incorrect A-Pillar Cover
Honda is recalling 2015 Fit vehicles because an incorrect A-pillar cover may impair side curtain air bag performance, increasing injury risk in a crash.
Product
HONDA — HONDA FIT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2085-2014·2014-07-30
GE Healthcare CARESCAPE Patient Monitors Recalled for Data Loss
GE Healthcare is recalling CARESCAPE B850, B650, and B450 patient monitors because the Patient Data Module may fail to communicate, causing partial loss of monitoring parameters.
Product
GE Healthcare, CARESCAPE Monitor B850, B650 or B450. Patient Monitor.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2111-2014·2014-07-30
Siemens syngo Imaging XS Software Recall for Potential Miscalculation
Siemens is recalling syngo Imaging XS software due to potential miscalculation of grey scale values in specific image processing functions.
Product
Siemens syngo Imaging XS, version VA70A or higher Syngo Imaging XS is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2091-2014·2014-07-30
Invacare Recalls M41 Wheelchair Controllers Due to Programming Error
Invacare is recalling 819 M41 powered wheelchair controllers that may cause momentary loss of control due to non-standard factory programming.
Product
MK5 NX Controller--Wheelchair controller
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2096-2014·2014-07-30
Terumo Recalls Sarns Venous Return Cannulae Due to Loose Fiber Particulate
Terumo CVS is recalling Sarns Malleable Dual-stage Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns Malleable Dual-stage Venous Return Cannulae 28/38, 32/40 & 34/46 Fr with 1/2" connector with or without Xcoating Product Usage: The Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2092-2014·2014-07-30
Alphatec Spine Recalls Solanas 2.1mm Fixed Depth Drill
Alphatec Spine is recalling 14 units of the Solanas 2.1mm Fixed Depth Drill because the golden stop slid from its fixed position during use.
Product
Solanas 2.1mm FIXED DEPTH DRILL, 10mm, Part No. 63928-10. Component of the SOLANAS III Posterior Stabilization System, a spinal fixation system intended to improve stability of the cervical and thoracolumbar area of the spine (C1-T3).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2099-2014·2014-07-30
Terumo Recalls Sarns Soft-Flow Aortic Cannulae Due to Fiber Particulate
Terumo CVS is recalling Sarns Soft-Flow Aortic Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or without luer & Xcoating, Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2098-2014·2014-07-30
Terumo Recalls Sarns Soft-arc Aortic Cannula Due to Loose Fiber Particulate
Terumo CVS is recalling 20 units of Sarns Soft-arc Aortic Cannulas because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns Soft-arc Aortic Cannula 8.0mm curved tip, suture flange, 3/8" flare Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2079-2014·2014-07-30
Siemens RAPIDPoint 500 Lactate Cartridges Recalled for Electrolyte Error Codes
Siemens Healthcare Diagnostics Inc is recalling RAPIDPoint 500 Lactate Cartridges because they may display error codes for electrolyte parameters.
Product
RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500 Measurement Cartridge Lactate (750 Tests) Part number: 10491449; RAPIDPoint 500 Measurement Cartridge Lactate (400 Tests) Part Number: 10491448 RAPIDPoint 500 Measurement Cartridge Lactate (250 Tests) Part…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2094-2014·2014-07-30
Terumo Recalls Sarns D4 Aortic Arch Cannulae Due to Particulate
Terumo CVS is recalling Sarns D4 Aortic Arch Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product Usage: The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2081-2014·2014-07-30
AGFA DX-D 100 X-Ray System Recalled for Touch Screen Malfunction
AGFA Corp. is recalling 216 DX-D 100 digital radiography systems because liquid contact with the touch screen may cause the device to incorrectly recognize user input and alter settings.
Product
AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2087-2014·2014-07-30
Synthes Orthopedic Guide Blocks Recalled for Incorrect Labeling
Synthes, Inc. is recalling 180 Guide Blocks for the Volar Distal Radius Plate System due to incorrect package labeling. The physical parts are correctly marked, but the packaging may identify the wrong side.
Product
Synthes Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius Plate System). Orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2196-2014·2014-07-30
Country Life Liquid Calcium Magnesium Supplement Recalled for Particulates
Country Life is recalling specific lots of its liquid calcium and magnesium dietary supplement because the product contains insoluble particulates that do not meet quality standards.
Product
Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex, WILD BLUEBERRY FLAVOR, LIQUID Dietary Supplement, 16 FL. OZ. (1 PINT) (472 mL), Product No. 2523, Bar Code 015794025238, and 32 FL. OZ. (1 QT) (944 mL), Product No. 2522, Bar code 015794025221 --- Manufactured…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2215-2014·2014-07-30
Kraft Recalls Knudsen, Breakstone's, and Other Cottage Cheese Brands
Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not stored at proper temperatures.
Product
Cottage Doubles - cottage cheese, 2% milkfat, with mango topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2106-2014·2014-07-30
Terumo CPB Catheter Kit Recalled for Loose Fiber Particulate
Terumo CVS is recalling 125 CPB Catheter Kits because in-process inspections found loose fiber particulate exceeding specifications.
Product
CPB Catheter Kit Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2216-2014·2014-07-30
Kraft Recalls Cottage Cheese Due to Improper Ingredient Storage
Kraft Foods is voluntarily recalling specific cottage cheese products because ingredients were not stored at proper temperatures, creating a potential safety risk.
Product
Cottage cheese, 2% milkfat, with pineapple sold under the Breakstone's brand or Knudsen brand and packaged in a tray of 4 plastic containers each with a net weight of 4 oz. (113 g).
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2097-2014·2014-07-30
Terumo Recalls Sarns Malleable Venous Return Cannulae Due to Particulate
Terumo CVS is recalling Sarns Malleable Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns Malleable Venous Return Cannulae 24, 28, 30, 32, 34, 36 & 40 Fr single stage with 3/8" & 1/2 flare with or without Xcoating Product Usage: The Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2105-2014·2014-07-30
Terumo Recalls Sarns Soft-Flow Aortic Cannulae Due to Fiber Particulate
Terumo CVS is recalling Sarns Soft-Flow Aortic Cannulae because in-process inspections found loose fiber particulate exceeding specifications.
Product
Sarns Soft-Flow Aortic Cannulae 6.0mm, 7mm & 8mm angled and straight tip, suture bulb with or without Luer and/or Xcoating Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2102-2014·2014-07-30
Terumo Dual-stage Venous Return Cannulae Recalled for Loose Fiber Particulate
Terumo CVS is recalling specific lots of venous return cannulae used in heart surgery due to loose fiber particulate found during inspection.
Product
Terumo Dual-stage Venous Return Cannulae 28/38, 29/37, 32/40, 34/46, 36/46 & 36/51 Fr with 1/2" flare or connector Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2217-2014·2014-07-30
Kraft Recalls Knudsen and Other Cottage Cheese Brands for Temperature Violations
Kraft Foods is voluntarily recalling multiple cottage cheese brands produced in California because ingredients were not stored at proper temperatures.
Product
Low fat cottage cheese, 1.5% milkfat, with pineapple sold under the Knudsen brand packaged in plastic containers with a net weight of 16 oz. (1 lb.) 453 g.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2211-2014·2014-07-30
Kraft Recalls Knudsen, Breakstone's, and Other Cottage Cheese Brands
Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not being stored at proper temperatures.
Product
Cottage Doubles - cottage cheese, 2% milkfat, with strawberry topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
Category
Food
Distribution
Distributed nationwide