State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34351–34375 of 73915

HighFDA (Devices)·Z-1081-2019·2019-04-10
Biomet Cement Plug Inserter Recalled for Sterilization Validation Issues
Zimmer Biomet is recalling 89 units of the Small Diameter Cement Plug Inserter due to a lack of adequate sterilization validation.
Product
Biomet Small Diameter Cement Plug Inserter-Sterile, single-use accessory instrumentation to be used during surgical procedures utilizing the Small Diameter Cement Plug implant devices Item Number: 414989
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V285000·2019-04-10
North Central Emergency Recalls Ambulances Due to Brake Light Wiring Defect
North Central Emergency is recalling 2016-2018 ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.
Product
NORTH CENTRAL EMERGENCY — NORTH CENTRAL EMERGENCY, CHEVROLET FORD E-350, FORD E-450, G4500, CHEVY G4500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1231-2019·2019-04-10
Fungi Perfecti Recalls Host Defense Blood Sugar Supplement for Undeclared Wheat
Fungi Perfecti LLC is recalling Host Defense MycoBotanicals Blood Sugar dietary supplements because they contain undeclared wheat. The recall affects 11,042 bottles distributed in the US, Canada, and Norway.
Product
Host Defense MycoBotanicals Blood Sugar, dietary supplement, 500mg capsules, 60 ct per bottle, serving size 2 capsules per day. UPC: 6 33422 70474 6 (distributed in US) UPC: 8 22078 71303 9 (distributed in Canada) The product is labeled in parts: "***HOST DEFENSE MYCO…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·19V288000·2019-04-10
Toyota Recalls 2019 Lexus ES for Driver Knee Air Bag Installation Defect
Toyota is recalling 2019 Lexus ES vehicles because the driver knee air bag assembly may have been improperly installed, potentially affecting deployment in a crash.
Product
LEXUS — LEXUS ES
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1077-2019·2019-04-10
Morphine Sulfate API Recalled for Microbial Contamination Out of Specification
Johnson Matthey Inc. is recalling Morphine Sulfate USP Milled API due to bioburden out of specification results.
Product
Morphine Sulfate USP Milled, Active Pharmaceutical Ingredient, Rx only, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1078-2019·2019-04-10
KRS Global Biotechnology Recalls Repinephrine IV Bags Due to Labeling Error
KRS Global Biotechnology is recalling 190 bags of Repinephrine 16 mg IV solution due to a label mix-up. The product was distributed nationwide.
Product
NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF), 16 mg / 250 mL, 250 mL IV bag, Rx only, KRS Global Biotechnology: 791 Park of Commerce Blvd., Boca Raton, FL 33487. NDC 3321678343
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1075-2019·2019-04-10
Abbott ARCHITECT Creatine Kinase IVD Recalled for Stability Issues
Abbott Laboratories is recalling specific lots of ARCHITECT Creatine Kinase IVD kits due to a stability issue that may cause error codes or out-of-range quality control results.
Product
Abbott ARCHITECT Creatine Kinase, IVD, REF 7D63-21.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1074-2019·2019-04-10
Jubilant Cadista Recalls Pantoprazole Sodium Tablets Due to Discoloration
Jubilant Cadista Pharmaceuticals is recalling 12,960 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on the tablet edges.
Product
Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx Only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801; NDC 59746-284-90.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1072-2019·2019-04-10
Pfizer Recalls Clindamycin Injection Vials Due to Impurity Failures
Pfizer is recalling specific lots of Clindamycin Injection due to high out-of-specification impurity results at the 24-month time point.
Product
Clindamycin Injection, USP, 900 mg/6 mL (150 mg/mL), 6 mL vial, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA. NDC 47781-621-94
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1069-2019·2019-04-10
Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures
Pfizer is recalling specific lots of Cleocin Phosphate injection because high levels of impurities were found at the 24-month time point.
Product
CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1071-2019·2019-04-10
Pfizer Recalls Clindamycin Injection Due to Impurity Specification Failures
Pfizer is recalling specific lots of Clindamycin Injection because high out-of-specification impurities were found at the 24-month time point.
Product
Clindamycin Injection, USP, 600 mg/ 4 mL (150 mg/mL), 4 mL vials, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC 47781-620-94
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1070-2019·2019-04-10
Pfizer Recalls Clindamycin Injection Vials Due to Impurity Failures
Pfizer is recalling specific lots of Clindamycin Injection because high levels of impurities were found at the 24-month time point.
Product
Clindamycin Injection, USP, 300 mg/ 2 mL (150 mg/mL), 2 mL vials, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA.,NDC 47781-619-94
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1079-2019·2019-04-10
KRS Global Biotechnology Recalls NORepinephrine IV Bags Due to Labeling Error
KRS Global Biotechnology is recalling 433 bags of NORepinephrine 4 mg in 5% Dextrose due to a label mix-up. The product was distributed nationwide.
Product
NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF), 4 mg / 250 mL, 250 mL IV bag, Rx only, KRS Global Biotechnology: 791 Park of Commerce Blvd., Boca Raton, FL 33487. NDC 3321674481
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1076-2019·2019-04-10
Abbott ARCHITECT Creatine Kinase IVD Recalled for Stability Issues
Abbott Laboratories is recalling 30 kits of ARCHITECT Creatine Kinase IVD due to a stability issue that may cause error codes or out-of-range quality control results.
Product
Abbott ARCHITECT Creatine Kinase, IVD, REF 7D6341.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1074-2019·2019-04-10
Abbott Recalls CELL-DYN Emerald Analyzers Due to Quality Control Errors
Abbott Laboratories is recalling 6,353 CELL-DYN Emerald analyzers worldwide because they may generate incorrect low quality control results for red blood cells and platelets.
Product
CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro diagnostic use in the clinical laboratory.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1068-2019·2019-04-10
Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures
Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurity levels were detected at the 24-month time point.
Product
CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1088-2019·2019-04-10
Beaver Visitec Recalls Micro Knife 5.0mm Due to Misprinted Expiration Date
Beaver Visitec is recalling 97 boxes of Micro Knife 5.0mm 30° instruments because the expiration date was misprinted as the lot number.
Product
Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1067-2019·2019-04-10
Pfizer Recalls Cleocin Phosphate Injection Due to Impurity Failures
Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurities were detected at the 24-month time point.
Product
CLEOCIN PHOSPHATE — CLEOCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V283000·2019-04-09
Proterra Recalls 2015-2018 Catalyst Buses Due to Brake Fire Risk
Proterra is recalling 2015-2018 Catalyst 40 buses because a clogged tow fitting cap can cause rear brakes to overheat and catch fire.
Product
PROTERRA — PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V282000·2019-04-09
Peterbilt 520 Recall: Undersized Wires May Cause Engine Shutdown
PACCAR is recalling 2017-2020 Peterbilt 520 trucks because undersized wires may overheat and melt, potentially causing an unexpected engine shutdown and increasing crash risk.
Product
PETERBILT — PETERBILT 520
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V281000·2019-04-09
Horton Ambulances Recalled for Reversed Backup Camera Image
Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Product
HORTON — HORTON TYPE I, TYPE III
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V284000·2019-04-09
Daimler Recalls 2019 Sprinter Vans for Headlight Sensor Calibration Issues
Daimler Vans USA is recalling 2019 Freightliner and Mercedes-Benz Sprinter vans because the headlamp range adjustment sensor may not be calibrated, potentially affecting driver visibility.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V276000·2019-04-09
AEV TraumaHawk Ambulances Recalled for Reversed Backup Camera Image
Halcore Group is recalling 2016-2019 AEV TraumaHawk ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.
Product
AEV — AEV TRAUMAHAWK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V280000·2019-04-09
Pierce Frontline Vehicles Recalled for Brake Light Wiring Defect
Pierce is recalling 2018-2019 Frontline C-35X, C-25, C-45X-3, and Encore Rescue vehicles because brake lights may illuminate without the pedal being pressed.
Product
FRONTLINE — FRONTLINE C-35X, C-25, ENCORE RESCUE, C-45X-3
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19102·2019-04-09
Marpac Recalls GO Travel Sleep Sound Machines Due to Burn Hazard
Marpac is recalling GO travel sleep sound machines because the internal battery can leak and cause an electrical short, posing a burn hazard.
Product
GO travel sleep sound machines
Category
Consumer Product
Distribution
Distributed nationwide