State

US Virgin Islands product recalls

73,376 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: 2026-09-23

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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20026–20050 of 73553

SevereFDA (Food)·F-1338-2022·2022-06-29
Peanut Butter Fudge Recalled for Potential Salmonella Contamination
Calico Cottage Inc is recalling peanut butter fudge products due to potential Salmonella contamination in the peanut butter ingredient. The recall affects bulk carton products distributed nationwide.
Product
1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer packaging, bulk carton 2. PEANUT BUTTER FUDGE (6S) 6LB NET WT- not consumer packaging, bulk carton 3. PEANUT BUTTER FUDGE (6SS) 6LB NET WT- not consumer packaging, bulk carton
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1271-2022·2022-06-29
Medfusion Syringe Pump Recalled Due to Multiple Infusion Control and Alarm Failures
Smiths Medical recalled 58,671 Medfusion Syringe Pump units worldwide due to multiple failures that could interrupt therapy or cause over-infusion, including defective alarms and display errors.
Product
Medfusion Syringe Pump Model: Model 4000-0100-50, Model 4000-0101-249, Model 4000-0101-50, Model 4000-0101-51, Model 4000-0101-78, Model 4000-0105-249, Model 4000-0105-51, Model 4000-0105-78, Model 4000-0106-00, Model 4000-0106-01, Model 4000-0106-231
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1321-2022·2022-06-29
Chocolate Peanut Butter Cups Recalled for Salmonella Contamination
Albanese Confectionery Group recalls Rich's Milk Chocolate peanut butter cups nationwide due to Salmonella contamination from recalled Jif peanut butter used in manufacturing.
Product
Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Rich s Milk Chocolate Mini Peanut Butter Cups; 2ct 5lb bulk per 10 lb case. Product not retail packaged, distributed for bulk sale at retail.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1337-2022·2022-06-29
Chocolate fudge with peanut butter recalled for potential Salmonella
Calico Cottage Inc is recalling chocolate fudge products containing peanut butter due to potential Salmonella contamination. The recall affects 677 units distributed nationwide.
Product
1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1272-2022·2022-06-29
Medfusion Syringe Pump Class I Recall: Risk of Over-Infusion or Therapy Interruption
Smiths Medical is recalling multiple Medfusion Syringe Pump models due to software and hardware defects that may interrupt drug infusion or cause over-infusion. Approximately 65,093 units distributed worldwide are affected.
Product
Medfusion Syringe Pump Models: 3500, 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82, 3500-306, 3500-402, 3500-414, 3500-415, 3500-500, 3500BC, 3500E, 3500G, 3500SD, 3500SD-500, 3500VX, 3500VX-306, 3500VX-414, 3500VX-415, 3500VX-500, 3500ZE…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1266-2022·2022-06-29
HeartWare HVAD Battery Model 1650DE May Malfunction Due to Weld Defect
Medtronic is recalling HeartWare HVAD batteries (Model 1650DE) due to an internal weld defect that can cause battery malfunction and prevent proper charging. Approximately 429 affected batteries were distributed worldwide.
Product
HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1340-2022·2022-06-29
Salted Nut Roll Fudge Recalled for Potential Salmonella in Peanut Butter
Calico Cottage Inc is recalling Salted Nut Roll Pre-Made Fudge nationwide because the peanut butter ingredient is potentially contaminated with Salmonella.
Product
1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk carton
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2022·2022-06-29
Colonovideoscope Model CF-H180AL recalled due to narrowed viewing angle
Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.
Product
Colonovideoscope Model CF-H180AL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1156-2022·2022-06-29
Tretinoin Capsules Recalled Nationwide for Failed Dissolution Specifications
Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.
Product
Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1153-2022·2022-06-29
Testosterone Cypionate Injectable Recalled for Manufacturing Quality Issues
Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1154-2022·2022-06-29
Testosterone Cypionate Injectable Recalled Due to Manufacturing Sterility Deviation
Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1345-2022·2022-06-29
Ice cream recall for undeclared tree nut allergen
Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.
Product
Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 ounce tub, UPC 0 77865 01001 7, Distributed by Associated Foods Stores, Salt Lake City, UT, 84119. Store Frozen.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1273-2022·2022-06-29
FDA Recalls Catheter Drainage Kits With Wrong Needle Size
Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.
Product
REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1347-2022·2022-06-29
Kava Glycerite Recalled Due to High Yeast and Mold Contamination
EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.
Product
Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (from Piper methysticum) and 9 mg Kavalactones (from Piper methysticum) depending on lot. Dosage: 60 drops 1-2 times a day. Product is packaged in Amber Glass Boston Round…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1151-2022·2022-06-29
Isopropyl Alcohol bottles recalled for defective containers and leakage
Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.
Product
ISOPROPYL ALCOHOL — ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1155-2022·2022-06-29
Clonazepam Tablets Recalled Due to Manufacturing Defect
Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.
Product
Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1281-2022·2022-06-29
BVI Wet-Field Eraser surgical devices shipped with incorrect tip configuration
Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.
Product
BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current Part Number: 221251
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V462000·2022-06-29
KZRV Recalls 2021 Escape Travel Trailers Due to Incorrect Tire Placard
KZRV is recalling 2021 Escape travel trailers because the tire placard lists incorrect information, which can lead to overinflated tires and increased crash risk.
Product
KZRV — KZRV ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1282-2022·2022-06-29
INTERGARD Woven Vascular Graft mislabeled with incorrect size specification
Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.
Product
INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1283-2022·2022-06-29
Cardiac device software recalled for inadequate electrical insulation
CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.
Product
CardioTek EP-TRACER Software V2.x.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1275-2022·2022-06-29
EVIS EXERA II Gastrointestinal Videoscope Recalled for Incorrect Component Fit
Olympus is recalling 8 EVIS EXERA II gastrointestinal videoscopes (Model GIF-HQ190) because an incorrect rubber component may have been installed during repair. The incorrect part does not meet the device's design specifications.
Product
EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model: GIF-HQ190
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1346-2022·2022-06-29
Wise Woman Herbals Kava Capsules recalled for yeast and mold contamination
EarthLab Inc is recalling Wise Woman Herbals Kava Capsules nationwide due to microbial contamination. Quality testing found yeast and mold counts that exceeded acceptable levels.
Product
Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3 times per day day at 450mg Kava root. 90 counts per bottle. UPC 7 48840 14284 8. Kava Capsules older lots are packaged in 250cc Wide Mouth Amber Glass Packer, Black 45/400 PP ribbed…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1348-2022·2022-06-29
Wise Woman Herbals Sleepytime Glycerite Recalled for Yeast and Mold Contamination
EarthLab Inc is recalling Wise Woman Herbals Sleepytime Glycerite due to elevated yeast and mold levels detected in microbial testing. Consumers should discontinue use.
Product
Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Boston Round bottle, Black serrated polypropylene dropper assembly with rubber bulb (2oz only) or Black…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1152-2022·2022-06-29
FDA Recalls Clonidine Transdermal Patches for Delivery System Defect
Mayne Pharma is recalling 1,440 cartons of Clonidine transdermal patches nationwide due to an out-of-specification defect in the release liner that could affect proper drug delivery.
Product
CLONIDINE — CLONIDINE (CLONIDINE)
Category
Drug
Distribution
Distributed nationwide
CriticalUSDA FSIS·020-2022·2022-06-28
Creminelli Recalls Mini Parmesan Salami Sticks Due to Undeclared Egg Allergen
Creminelli Fine Meats is recalling approximately 4,207 pounds of mini parmesan salami sticks because the product contains an undeclared egg allergen.
Product
Creminelli Operating LLC — Creminelli Fine Meats Recalls Mini Parmesan Salami Stick Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide