State

US Virgin Islands product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33876–33900 of 73912

SevereFDA (Devices)·Z-1267-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery Inc is recalling Curved Intraluminal Staplers, Model CDH21A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Curved Intraluminal Staplers, 21 mm diameter, Model CDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1386-2019·2019-05-22
AmeriHerb Mullein Leaf Recalled for Potential E. coli Contamination
AmeriHerb International Inc is recalling 144 lbs of Mullein leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.
Product
Mullein leaf c/s, Verbascum Thapsus, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·19V384000·2019-05-22
Newmar Recalls 2019 Motorhomes Due to Loose Brake Caliper Bolts
Newmar is recalling 2019 Mountain Aire and Essex motorhomes because loose brake caliper mounting bolts may reduce brake effectiveness and increase crash risk.
Product
NEWMAR — NEWMAR ESSEX, MOUNTAIN AIRE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1272-2019·2019-05-22
Ethicon Endo-Surgery Recalls Endoscopic Curved Intraluminal Staplers
Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers (Model ECS25A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Endoscopic Curved Intraluminal Stapler, 25 mm diameter, Model ECS25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1276-2019·2019-05-22
Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH25A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Straight Intraluminal Staplers, 25 mm diameter, Model SDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1388-2019·2019-05-22
AmeriHerb Goldenseal Herb Recalled for Potential E. coli Contamination
AmeriHerb International Inc is recalling 36 lbs of Goldenseal herb due to potential contamination with generic E. coli. The product was distributed nationwide and to Canada.
Product
Goldenseal herb c/s, Hydrastis Canadensis, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1269-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery Inc is recalling 434,614 Curved Intraluminal Staplers (Model CDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Curved Intraluminal Staplers, 29 mm diameter, Model CDH29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1274-2019·2019-05-22
Ethicon Endo-Surgery Recalls 33 mm Endoscopic Curved Intraluminal Staplers
Ethicon Endo-Surgery Inc is recalling 434,614 Model ECS33A staplers worldwide because they may have an insufficient firing stroke to break the washer and form staples.
Product
Endoscopic Curved Intraluminal Stapler, 33 mm diameter, Model ECS33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1337-2019·2019-05-22
Terumo Electronic Patient Gas System Recalled for Inaccurate Gas Flow Rate
Terumo is recalling 1,258 Electronic Patient Gas Systems because a flowmeter defect may cause inaccurate gas flow rate output.
Product
Terumo Advanced Perfusion System 1 Electronic Patient Gas System, Catalog # 801188, UDI 00886799000588 The electronic gas blender provides control and monitoring of the gas flow rate and oxygen content of the gas input to the oxygenator in the perfusion circuit.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1321-2019·2019-05-22
Philips SureSigns VS3 Monitor Recall Due to Software Defect
Philips is recalling SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Product
SureSigns VS3 NBP, SpO2, Temp, Product Number 863073. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1354-2019·2019-05-22
Abbott Alinity i Estradiol Reagent Kit Recalled for False Results
Abbott Ireland Diagnostics Division is recalling Alinity i Estradiol Reagent Kits because patient results may be falsely elevated for individuals treated with Mifepristone.
Product
Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity i Estradiol assay is a chemiluminescent microparticle immunoassay (CMIA) used for the quantitative The determination of Estradiol in serum and plasma on the Alinity i analyzer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1319-2019·2019-05-22
Philips SureSigns VS3 Monitor Recall for High Pulse Rate Measurement Failure
Philips is recalling SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Product
SureSigns VS3 NBP, SpO2, Product Number 863071. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1314-2019·2019-05-22
BD Veritor System Reader Recalled for Potential False Test Results
Becton Dickinson is recalling 124 BD Veritor System Readers due to background calibration issues that may cause false positive or negative test results.
Product
BD Veritor System Reader -In Vitro Diagnostic for use with BD Veritor System Test Kit Devices Catalog Number: 256055
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1330-2019·2019-05-22
Shippert Medical Technologies Recalls Tissu-Trans FILTRON 100 Due to Pouch Integrity Concerns
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 100 sterile pouches because a cut or hole may compromise the product's sterility.
Product
Tissu-Trans FILTRON 100, Catalog 3-TT-FILTRON 100, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1322-2019·2019-05-22
Philips SureSigns VS3 Monitor Software Defect Recall
Philips is recalling SureSigns VS3 patient monitors because a software defect prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Product
SureSigns VS3 NBP, SpO2, Temp, Rec, Product Number 863074. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1339-2019·2019-05-22
Siemens Artis Zee Angiography Systems Recalled for Tabletop Movement Blockage
Siemens is recalling 459 Artis Zee angiography systems because the floating tabletop movement may be blocked after a collision sensor is activated.
Product
Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is 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
HighFDA (Food)·F-1383-2019·2019-05-22
AmeriHerb Parsley Flakes Recalled for Potential E. coli Contamination
AmeriHerb International Inc is recalling 256 lbs of parsley flakes potentially contaminated with E. coli. The product was distributed nationwide and to Canada.
Product
Parsley flakes, Petroselinum sativum, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1313-2019·2019-05-22
BD Veritor Plus Analyzer Recalled for Potential Test Result Errors
Becton Dickinson & Co. is recalling 32 BD Veritor Plus Analyzers because background calibration issues may cause false positive or negative test results.
Product
BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devices. Catalog Number: 256066
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1340-2019·2019-05-22
Siemens Artis Zeego Angiography Systems Recalled for Tabletop Movement Blockage
Siemens is recalling 459 Artis Zeego angiography systems because the floating tabletop movement may be blocked after a collision sensor activates.
Product
Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1336-2019·2019-05-22
Shippert Medical Technologies Recalls Tissu-Trans Syringe Fill 360 Due to Pouch Integrity Concerns
Shippert Medical Technologies is recalling Tissu-Trans Syringe Fill 360 devices because the sterile pouch integrity cannot be assured without visual examination.
Product
Tissu-Trans Syringe Fill 360, Catalog 3-TT-SFILL 360, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1333-2019·2019-05-22
Shippert Medical Technologies Recalls Tissu-Trans FILTRON 1000 Medical Devices
Shippert Medical Technologies is voluntarily recalling 6,553 units of Tissu-Trans FILTRON 1000 sterile, disposable, one-patient use devices due to a Class II safety concern.
Product
Tissu-Trans FILTRON 1000, Catalog 3-TT-FILTRON 1000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1332-2019·2019-05-22
Shippert Medical Technologies Recalls Tissu-Trans FILTRON 500 Due to Pouch Integrity Concerns
Shippert Medical Technologies is recalling Tissu-Trans FILTRON 500 sterile pouches because a cut or hole in the packaging may compromise the product's sterility.
Product
Tissu-Trans FILTRON 500, Catalog 3-TT-FILTRON 500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1320-2019·2019-05-22
Philips SureSigns VS3 Monitor Software Defect Recall
Philips is recalling 3,177 SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Product
SureSigns VS3 NBP, SpO2, Rec, Product Number 863072. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V389000·2019-05-22
Volkswagen Recalls Passat and Atlas Vehicles for Headlight Adjustment Defect
Volkswagen is recalling 2012-2020 Passat and 2018-2019 Atlas vehicles because a missing blocking cap allows headlight aim to be adjusted out of specification, increasing crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN PASSAT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1324-2019·2019-05-22
Philips SureSigns VS4 Monitor Software Defect Recall
Philips is recalling 366 SureSigns VS4 monitors because software prevents the device from measuring or alarming for pulse rates above 240 beats per minute.
Product
SureSigns VS4 Government Bundle, Product Number 863286. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature).
Category
Medical Device
Distribution
Distributed nationwide