State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28801–28825 of 73774

ModerateFDA (Devices)·Z-2142-2020·2020-06-03
Inpeco Aptio Automation System Recalled for Sample Association Error
Inpeco S.A. is recalling 70 Aptio Automation Systems with specific interface modules due to a firmware communication error that can cause erroneous sample-tube associations.
Product
Aptio Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00) - Product Usage: is a modular system designed to automate Pre-Analytical and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2129-2020·2020-06-03
Teleflex Recalls Sprotte Lumbar Puncture Needles Due to Sterility Concerns
Teleflex Medical is recalling 4,227 Sprotte lumbar puncture needles because a packaging issue prevents the manufacturer from guaranteeing their sterility.
Product
Sprotte Needle, REF 32115130C w/ Intro 22 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needles are intended to gain entry into or puncture the spinal cavity permitting injection (including anesthesia) / withdrawal of fluids for purposes of diagnostic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1276-2020·2020-06-03
PD-Rx Recalls Doxycycline Hyclate Tablets for Failed Dissolution Specifications
PD-Rx Pharmaceuticals is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications. The recall covers 14,030 bottles distributed nationwide.
Product
DOXYCYCLINE — DOXYCYCLINE (DOXYCYCLINE HYCLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2130-2020·2020-06-03
Teleflex Recalls Sprotte Lumbar Puncture Needles Due to Sterility Concerns
Teleflex Medical is recalling 800 Sprotte lumbar puncture needles because a packaging issue prevents the manufacturer from guaranteeing sterility.
Product
Sprotte Needle, REF 33115131B w/ Intro 20 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needles are intended to gain entry into or puncture the spinal cavity permitting injection (including anesthesia) / withdrawal of fluids for purposes of diagnostic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1278-2020·2020-06-03
LidoPro Patches Recalled Due to Missing Manufacturing Records
Wuhan Bingbing Pharmaceutical is recalling LidoPro patches because manufacturing records and samples were lost, preventing verification of product stability.
Product
LidoPro (lidocaine 4%, menthol 5%, methyl salicylate 4%) patch, 15 Patches per box, Manufactured For: Terrain Pharmaceuticals, Reno, NV 89501; NDC 53225-1023-1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1277-2020·2020-06-03
LidoPatch Pain Relief Patches Recalled Due to Missing Manufacturing Records
Wuhan Bingbing Pharmaceutical is recalling LidoPatch pain relief patches because missing manufacturing records prevent verification that the product remains within specification through its expiration date.
Product
LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30 patches/box (NDC 10882-527-02 and 10882-527-04), Manufactured for: JAR Laboratories, Elmhurst, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0959-2020·2020-06-03
Siete Grain Free Cashew Flour Tortillas Recalled for Foreign Material
Garza Food Ventures is recalling Siete Grain Free Cashew Flour Tortillas due to a potential to contain foreign material.
Product
Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8 Count UPC 865336000045 packaged in flexible plastic
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1279-2020·2020-06-03
Mencaine Lidocaine Patches Recalled Due to Missing Manufacturing Records
Wuhan Bingbing Pharmaceutical is recalling Mencaine patches because manufacturing records and samples were lost, preventing verification that the product remains within specification through expiration.
Product
Mencaine (lidocaine 4.5%, menthol 5%) Patch, 1 patch per pouch, Manufactured For: Terrain Pharmaceuticals, Reno, NV 89501; NDC 53225-1090-1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0962-2020·2020-06-03
Jindilli Beverages Recalls Milkadamia Unsalted Buttery Spread for Potential Mold
Jindilli Beverages LLC is recalling Milkadamia Unsalted Buttery Spread due to the potential to contain mold. The product was distributed nationwide.
Product
Milkadamia Unsalted Buttery Spread 8 ounces packaged in plastic tub, 6 packaged per case UPC 858045004725
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2111-2020·2020-06-03
GE Healthcare Recalls Giraffe Shuttle Upgrade Kits Due to Battery Odor
GE Healthcare is recalling Giraffe Shuttle upgrade kits because the batteries emit a strong sulfur odor during charging.
Product
Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0963-2020·2020-06-03
Jindilli Beverages Recalls Milkadamia Salted Buttery Spread for Potential Mold
Jindilli Beverages LLC is recalling 2,981 cases of Milkadamia Salted Buttery Spread due to the potential presence of mold.
Product
Milkadamia Salted Buttery Spread 8 ounces packaged in plastic tub, 6 packaged per case UPC 858045004718
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1280-2020·2020-06-03
CVS Lidocaine Cold and Hot Patch Recalled for Manufacturing Record Loss
CVS Pharmacy is recalling Maximum Strength Lidocaine Cold & Hot Patches because manufacturing records and samples were lost, meaning the product may not remain within specification through its expiration date.
Product
Maximum Strength Lidocaine Cold & Hot Patch (lidocaine 4%, menthol 1%), 5 patches per box, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895; NDC 66902-218-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1274-2020·2020-06-03
West-Ward Recalls Doxycycline Hyclate Tablets Due to Dissolution Failure
West-Ward Columbus Inc. is recalling Doxycycline Hyclate 100 mg tablets because they failed a dissolution test at the end of their shelf life.
Product
DOXYCYCLINE HYCLATE — DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2140-2020·2020-06-03
Inpeco FlexLab Automation System Recalled for Sample Association Errors
Inpeco S.A. is recalling 37 FlexLab Automation Systems due to a firmware communication error that can cause sample tubes to be incorrectly associated with carriers.
Product
FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00)is a modular system designed to automate Pre-Analytical and Post-Analytical…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V321000·2020-06-02
Bentley Recalls 2019-2020 Bentayga Vehicles Due to Fuel Line Leak Risk
Bentley is recalling 1,892 2019-2020 Bentayga vehicles because a fuel line connector may leak, increasing the risk of fire.
Product
BENTLEY — BENTLEY BENTAYGA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V320000·2020-06-01
Keystone Recalls 2020 Springdale Trailers Due to Incorrect Axles and Tires
Keystone RV Company is recalling 2020 Springdale trailers because they were equipped with incorrect axles and tires, which may cause the trailer to be overloaded and increase the risk of a crash.
Product
KEYSTONE — KEYSTONE SPRINGDALE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20T009000·2020-06-01
Vee Tyre Recalls Taiga A/T Tires Due to Sidewall Separation Risk
Vee Tyre is recalling 522 Taiga A/T tires because the sidewall may separate, increasing the risk of a crash.
Product
TIRES:SIDEWALL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V317000·2020-05-29
Forest River Recalls 2020-2021 Cargo Trailers Due to Safety Chain Defect
Forest River is recalling 2020-2021 US Cargo, Haulin', and Trail & Sport cargo trailers because safety chains may break if the trailer becomes unhitched.
Product
US CARGO — US CARGO, HAULIN' CARGO TRAILER, TRAIL & SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V316000·2020-05-29
Braun Ambulances Recall 2019 Models Due to Rear Brake Line Wear
Braun Ambulances is recalling 2019 Chief XL and Liberty ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
Product
BRAUN AMBULANCES — BRAUN AMBULANCES CHIEF XL TYPE I, LIBERTY TYPE I
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V319000·2020-05-29
GM Recalls 2019-2020 Chevrolet HD Trucks for ABS Warning Light Defect
General Motors is recalling 2019-2020 Chevrolet 4500HD, 5500HD, and 6500HD trucks because the ABS malfunction light may fail to illuminate, increasing crash risk.
Product
INTERNATIONAL MOTORS — INTERNATIONAL MOTORS CHEVY 5500HD, CHEVY 4500HD, CHEVY 6500HD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V313000·2020-05-28
Frazer Recalls 2019-2020 RAM Chassis Emergency Vehicles for Brake Line Wear
Frazer is recalling 2019-2020 emergency vehicles on RAM 4500 and 5500 chassis because rear brake lines may wear, causing brake failure and increasing crash risk.
Product
FRAZER — FRAZER RAM 4500 CHASSIS, RAM 5500 CHASSIS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V314000·2020-05-28
Honda and Acura Recall Vehicles for Fuel Pump Failure Risk
Honda is recalling specific 2018-2020 models because a faulty fuel pump may cause the engine to stall while driving, increasing crash risk.
Product
HONDA — HONDA, ACURA ACCORD, INSIGHT, CIVIC, RLX HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·011-2020·2020-05-28
Nestle Recalls Lean Cuisine Fettuccini Alfredo for Undeclared Allergens
Nestle Prepared Foods is recalling Lean Cuisine Fettuccini Alfredo products because they contain undeclared soy and chicken, which are not listed on the label.
Product
Nestle Prepared Foods Company — Nestle Prepared Foods Company Recalls Lean Cuisine Fettuccini Alfredo Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·20V312000·2020-05-28
Thor Motor Coach Recalls 2020 Motorhomes for Brake Hose Chafing Risk
Thor Motor Coach is recalling 566 2020 motorhomes because a fender liner may chafe the brake hose, potentially causing brake fluid loss and increased braking distance.
Product
THOR MOTOR COACH — THOR MOTOR COACH CHATEAU CITATION, SIESTA, TIBURON, COMPASS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V315000·2020-05-28
Nissan Recalls 2013-2018 Altima Vehicles for Hood Latch Corrosion Risk
Nissan is recalling 2013-2018 Altima vehicles because the secondary hood latch may corrode and fail, potentially allowing the hood to open while driving.
Product
NISSAN — NISSAN ALTIMA
Category
Vehicle
Distribution
Distributed nationwide