State

US Virgin Islands product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26276–26300 of 73744

ModerateFDA (Devices)·Z-0808-2021·2021-01-20
Clerio Vision Contact Lenses Recalled for Incorrect Power Labeling
Clerio Vision is recalling one lot of contact lenses because the packaging labeled them as -2.25 power, but the lenses inside are -3.75 power.
Product
Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and UPC 675506804478 (12 count) - Product Usage: for daily wear is indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0231-2021·2021-01-20
Genus Lifesciences Recalls Oxycodone Hydrochloride Oral Solution Due to Particulate Matter
Genus Lifesciences Inc. is recalling Oxycodone Hydrochloride Oral Solution because particulate matter was found in multiple lots. The product was distributed nationwide in the USA.
Product
OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0221-2021·2021-01-20
Akorn Recalls Levetiracetam Oral Solution Due to Leaking Bottles
Akorn, Inc. is recalling specific lots of Levetiracetam Oral Solution because customer complaints reported the liquid leaking from the bottles.
Product
Levetiracetam Oral Solution, 100 mg/mL, 16 fl oz (473 mL) bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY 11701; NDC 50383-241-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0771-2021·2021-01-20
Siemens SOMATOM CT Scanner Software Recall for Scan Parameter Issues
Siemens is recalling specific SOMATOM CT scanner systems due to a software issue that may prevent scan cancellation and reloading, potentially delaying diagnosis or requiring patient rescans.
Product
SOMATOM Force, Definition AS, Definition Edge, Definition Flash, Drive, Confidence and Edge Plus
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0807-2021·2021-01-20
Baxter Recalls VERITAS Collagen Matrix Patches Due to Undersized Width
Baxter Healthcare is recalling 192 units of VERITAS Collagen Matrix patches because they may have undersized width dimensions. The recall covers US and international distribution.
Product
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0847-2021·2021-01-20
Visby Medical Recalls 282 COVID-19 Test Kits for Labeling Errors
Visby Medical is recalling 282 COVID-19 test kits because some boxes incorrectly state the product is CLIA Waived and some components expire before the kit expiration date.
Product
visby medical COVID-19 Test kit *** An in vitro diagnostic for the qualitative detection of SARS-CoV-2 - Product Usage: The Visby Medical COVID-19 Test is only for use under the Food and Drug Administration s Emergency Use Authorization.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0844-2021·2021-01-20
Ortho VITROS Chemistry TP Slides Recalled for Eltrombopag Interference
Ortho Clinical Diagnostics is recalling VITROS Chemistry TP Slides because the drug eltrombopag can interfere with total protein measurements.
Product
VITROS Chemistry Products TP Slides- IVD measure total protein (TP) concentration in serum and plasma using VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems Product Code: 8392292
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0860-2021·2021-01-20
Medtronic Intellis Spinal Cord Stimulator Software Recall
Medtronic is recalling the Intellis Spinal Cord Stimulator software due to a defect that prevents clinicians from programming the implantable neurostimulation device.
Product
Medtronic Intellis Spinal Cord Stimulator, Model Number A710, Clinical Programmer application version 1.3.80 - Product Usage: intended for use by clinicians in the programming of the following Medtronic neurostimulators (external and implantable) for pain therapy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0845-2021·2021-01-20
Ortho Clinical Diagnostics Recalls VITROS XT Chemistry Products ALB-TP Slides
Ortho Clinical Diagnostics is recalling VITROS XT Chemistry Products ALB-TP Slides due to potential interference from the drug eltrombopag.
Product
VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) - IVD quantitatively measures total protein (TP) concentration in serum and plasma using VITROS XT 3400 Chemistry Systems and VITROS XT 7600 Integrated Systems Product Code: 6844293
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0224-2021·2021-01-20
KVK-Tech Recalls Benzhydrocodone and Acetaminophen Tablets Due to Impurity
KVK-Tech, Inc. is recalling 528 bottles of Benzhydrocodone and Acetaminophen Tablets because the N-Oxide impurity exceeded specifications during stability testing.
Product
Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets, Rx Only, Manufactured for: KVK-Tech, Inc., Newtown, PA 18940 USA, NDC 10702-344-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0223-2021·2021-01-20
US Compounding Recalls Succinylcholine Chloride Injection Due to Labeling Error
US Compounding Inc is recalling 1,534 syringes of Succinylcholine Chloride Injection because the lot number and expiration date were printed in the wrong position, making them illegible.
Product
Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes, Rx only, US Compounding, 1270 Don's Lane, Conway, AR 72032
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·21070·2021-01-19
Rapala Recalls Rechargeable Fillet Knives Due to Fire Hazard
Rapala USA is recalling about 128,000 rechargeable fillet knives because the batteries can overheat and catch fire if non-Rapala chargers are used.
Product
Rapala® Rechargeable Fillet Knives (Item No. RRFN)
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21E004000·2021-01-19
Auxbeam Headlight Bulb Recall for Excessive Glare and Brightness
Guangzhou Zhilan E-Commerce is recalling specific Auxbeam headlight bulbs sold on Amazon that may create excessive glare for oncoming drivers, increasing crash risk.
Product
EXTERIOR LIGHTING:HEADLIGHTS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·002-2021·2021-01-15
Nestlé Prepared Foods recalls pepperoni hot pockets due to possible foreign matter contamination
The USDA Food Safety and Inspection Service is recalling approximately 762,615 pounds of not-ready-to-eat pepperoni hot pockets because they may contain glass and hard plastic fragments. One consumer reported a minor oral injury, but no additional illness cases were reported.
Product
Nestlé Prepared Foods Recalls Not-Ready-to-Eat Pepperoni Hot Pockets Product Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·21V014000·2021-01-15
Ford Recalls 2020 Explorer Police Interceptor and Lincoln Aviator for Washer Fluid Contamination
Ford is recalling 2020 Explorer Police Interceptor Utility and Lincoln Aviator vehicles because their windshield washer fluid was contaminated with brake fluid, which can reduce visibility and increase crash risk.
Product
FORD — FORD, LINCOLN EXPLORER POLICE INTERCEPT, AVIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V011000·2021-01-15
Ford Escape rear drive axle lubricant defect may cause loss of control
Ford is recalling approximately 147 2020 Ford Escape vehicles and related models due to inadequate lubricant in the rear drive unit, which may cause the rear axle to seize and result in loss of vehicle control and crash risk.
Product
FORD — FORD, LINCOLN ESCAPE, CORSAIR, EDGE, NAUTILUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V013000·2021-01-15
2021 KZRV Recreational Trailers Recalled for Improper Microwave Circuit Protection
KZRV recalls 2021 Escape, Sonic, and Sportsmen Classic trailers with microwave circuits on improper 20-amp circuit breakers (should be 15-amp), creating fire risk. Owners should request free replacement from KZRV.
Product
KZRV — KZRV ESCAPE, SONIC, SPORTSMEN CLASSIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V012000·2021-01-15
Altec Recalls 2016-2020 Digger Derricks for Missing Capacity Charts
Altec is recalling 213 digger derricks from 2016-2020 that lack the required combined use capacity chart, posing an injury risk to operators.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V010000·2021-01-14
2019-2021 Honda Odyssey fuel tank assembly recall due to fire risk
Braun Corporation is recalling certain 2018-2021 Honda Odyssey vehicles due to a fuel tank assembly defect that may cause fuel leaks, creating a potential fire risk. No injuries have been reported.
Product
HONDA — HONDA ODYSSEY
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21719·2021-01-14
Scalpa Numb Topical Anesthetic Cream Recalled for Child-Resistant Packaging Failure
Scalpa Inc. is recalling Scalpa Numb Maximum Strength Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, posing a poisoning risk to young children.
Product
Scalpa Numb Maximum Strength Topical Anesthetic Cream
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V009000·2021-01-14
2021 Heartland Mallard recreational trailers recalled for suspension defect
Heartland is recalling certain 2021 Mallard M180BH recreational trailers with incorrect axle, rims, and tires that can cause overloading and increase crash risk. Free replacement parts are available.
Product
HEARTLAND — HEARTLAND MALLARD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0203-2021·2021-01-13
SCA Pharmaceuticals Recalls Neostigmine Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 390 syringes of neostigmine methylsulfate due to a lack of assurance of sterility and potential defective caps.
Product
neostigmine methylsulfate 5 mg/5 mL, (1mg/ml), Rx Only, 5 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004075009
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0212-2021·2021-01-13
SCA Pharmaceuticals Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 5,067 syringes of Succinylcholine Chloride 100 mg/5mL due to a lack of assurance of sterility and potential defective caps.
Product
SUCcinylcholine Chloride 100 mg/5mL, Rx Only, 5 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., WIndsor, CT, 06095, barcode 70004090809
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0204-2021·2021-01-13
SCA Pharmaceuticals Recalls Phenylephrine Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 23,029 syringes of Phenylephrine HCl due to a lack of assurance of sterility and potential defective caps.
Product
PHENYLephrine HCl 1000 mcg/10 mL in 0.9% Sodium Chloride, (100 mcg/mL) Rx Only, 10 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004081012
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0197-2021·2021-01-13
SCA Pharmaceuticals Recalls Ketamine Injection Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 11,075 syringes of Ketamine 100 mg/10mL injection due to a lack of assurance of sterility and potential defective syringe caps.
Product
Ketamine 100 mg/10mL in 0.9% Sodium Chloride Injection (10 mg/mL), CII, Rx Only, 10 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004043012
Category
Drug
Distribution
Distributed nationwide