State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42951–42975 of 73919

SevereFDA (Devices)·Z-2226-2017·2017-06-14
Magellan LeadCare Blood Test Kits Underestimate Lead Concentrations
Magellan Diagnostics is recalling LeadCare Ultra and Plus test kits because they may underestimate lead levels in venous blood samples.
Product
Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product Usage: The LeadCare Blood Lead Test Kit is for in vitro diagnostic use only. The Test Kit is for the quantitative measurement of lead in fresh whole blood. This product is for professional use only.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0894-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 12.5 mg pellets due to CGMP deviations and a lack of quality assurance. The recall covers 4,883 pellets distributed nationwide.
Product
Estradiol 12.5 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013, NDC: 69761-012-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2302-2017·2017-06-14
Arrow Arterial Line Kits Recalled for Needlestick Injury Risk
Arrow International is recalling Arterial Line Kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0890-2017·2017-06-14
Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations
Qualgen is recalling Estradiol 22 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 1,666 pellets distributed nationwide.
Product
Estradiol 22 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-022-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2290-2017·2017-06-14
Arrow International Recalls Access Kits Due to Needlestick Injury Risk
Arrow International is recalling specific Access Kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Arrow¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr. Peripherally Inserted Central Venous Catheter The Arrow¿ GlideThru" Peel-Away Sheath/Dilator Introducer is used for the percutaneous introduction of diagnostic or therapuetic devices into the vasculature
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0882-2017·2017-06-14
Spectrum Chemical Recalls Levonorgestrel API Due to CGMP Deviations
Spectrum Laboratory Products is recalling levonorgestrel active pharmaceutical ingredient due to manufacturing deviations found by the FDA.
Product
Levonorgestrel, U.S.P. active pharmaceutical ingredient, packaged in 1 kg container, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901, Product code L1229.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2269-2017·2017-06-14
Arrow Pressure Injectable PICC Kit Recalled for Needlestick Injury Risk
Arrow International is recalling 43,394 units of Pressure Injectable PICC Kits nationwide due to reports of safety cover disengagement and needlestick injuries.
Product
Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2260-2017·2017-06-14
Arrow International Recalls Hemodialysis Catheter Kits Due to Needlestick Risk
Arrow International is recalling 43,394 hemodialysis catheterization kits nationwide because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Two-Lumen Hemodialysis Catheterization Kit with Blue Flex Tip(R), ARROWg+ard Blue(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions for High Volume Infusions. The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R) permits venous access…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2256-2017·2017-06-14
Arrow International Recalls Pressure Injectable PICC Kits Due to Needlestick Risk
Arrow International is recalling Pressure Injectable PICC Kits because the packaged BD Eclipse Needle has a safety cover that may disengage, posing a needlestick injury risk.
Product
Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2301-2017·2017-06-14
Arrow QuickFlash Radial Artery Catheterization Kit Recalled for Needlestick Risk
Arrow International is recalling QuickFlash Radial Artery Catheterization Kits because the packaged BD Eclipse Needle may disengage, posing a needlestick injury risk.
Product
QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2270-2017·2017-06-14
Arrow International Recalls CVC Kits Due to Needlestick Injury Risk
Arrow International is recalling ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kits because packaged BD Eclipse Needles may disengage, posing a needlestick injury risk.
Product
ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit. The large-bore multiple-lumen catheter permits venous access to the central circulation for rapid fluid administration. It ma be inserted into the jugular, subclavian or femoral veins
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2276-2017·2017-06-14
Arrow Catheter Kits Recalled for Needlestick Injury Risk
Arrow International is recalling catheterization kits because the packaged BD Eclipse Needle has a safety cover that can disengage, causing needlestick injuries.
Product
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2317-2017·2017-06-14
Aunt Jemima Cinnamon Swirl French Toast Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Cinnamon Swirl Thick French Toast nationwide due to potential Listeria monocytogenes contamination.
Product
Aunt Jemima(R) Cinnamon Swirl Thick French Toast, 144 COUNT, NET WT 10.7 LBS, UPC 001960043584
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2300-2017·2017-06-14
Aunt Jemima Homestyle French Toast Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Homestyle French Toast due to potential Listeria monocytogenes contamination.
Product
AUNT JEMIMA(R) HOMESTYLE FRENCH TOAST, 6 COUNT, NET WT 12.5oz, UPC 019600057703
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2017·2017-06-14
Arrow International Recalls Hemodialysis Catheterization Kits
Arrow International Inc. is recalling ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kits due to a Class II recall.
Product
ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2315-2017·2017-06-14
Aunt Jemima Whole Grain Mini Pancakes Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Whole Grain Mini Pancakes due to a potential for Listeria monocytogenes contamination.
Product
Aunt Jemima(R) Whole Grain Mini Pancakes, 12-40 COUNT, NET WT 12 LBS, UPC 001960043558
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2314-2017·2017-06-14
Aunt Jemima Cinnamon Swirl French Toast Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Cinnamon Swirl French Toast due to potential Listeria monocytogenes contamination.
Product
Aunt Jemima(R) Cinnamon Swirl French Toast, 144 COUNT, NET WT 13.5 LBS, UPC001960005880
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2317-2017·2017-06-14
DePuy Synthes Orthopedic Instruments Recalled for Quality System Violations
DePuy Orthopaedics is recalling 345 orthopedic instruments modified by U.S. distributors because they were made outside quality system regulations, potentially compromising safety and effectiveness.
Product
DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various orthopedic procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2271-2017·2017-06-14
Arrow International Recalls Central Venous Catheter Kits Due to Needlestick Risk
Arrow International is recalling specific central venous catheter kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.
Product
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions requiring central venous access including, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2307-2017·2017-06-14
Pinnacle Foods Recalls Aunt Jemima Mini Pancakes for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Mini Pancakes due to a potential for Listeria monocytogenes contamination. The recall covers 8,344 units distributed nationwide.
Product
AUNT JEMIMA(R) MiNi pancakes, MAPLE BLAST, NET WT 3.2 OZ, UPC 001960043563
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2318-2017·2017-06-14
Zimmer Biomet Recalls Vitality Spinal Fixation System Drivers
Zimmer Biomet is recalling Vitality T27 Final Drivers and Torque Limiting Handles because they may create torsional springs that damage the device or cause torque values to go out of specification.
Product
Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2017·2017-06-14
Arrow QuickFlash Radial Artery Catheterization Kit Recalled for Needlestick Risk
Arrow International is recalling QuickFlash Radial Artery Catheterization Kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
QuickFlash Radial Artery/Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2294-2017·2017-06-14
Arrow International Recalls Femoral Arterial Line Catheterization Kits
Arrow International is recalling specific femoral arterial line catheterization kits due to reports of safety cover disengagement and needlestick injuries associated with packaged BD Eclipse Needles.
Product
Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2292-2017·2017-06-14
Aunt Jemima Blueberry Mini Pancakes Recalled for Listeria Risk
Pinnacle Foods is recalling Aunt Jemima Lil' Griddles Blueberry Mini Pancakes due to a potential for Listeria monocytogenes contamination.
Product
AUNT JEMIMA(R) LIL' GRIDDLES(TM) BLUEBERRY MINI PANCAKES, 40 COUNT, NET WT 14.5oz UPC 019600054603
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2255-2017·2017-06-14
Arrow International Recalls Central Venous Access Kits Due to Needlestick Risk
Arrow International is recalling specific Central Venous Access Kits because the packaged BD Eclipse Needle may disengage, posing a needlestick injury risk.
Product
ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit The MAC(TM) Multi-Lumen Central Venous Access Device with ARROWg+ard Blue(R) permits venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins.…
Category
Medical Device
Distribution
Distributed nationwide