State

US Virgin Islands product recalls

72,913 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: 30
Most recent: 2026-09-09

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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1676–1700 of 73090

SevereFDA (Devices)·Z-2218-2026·2026-05-27
Medtronic DLP Retrograde Cannula Recalls for Sterile Barrier Breach Risk
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0819-2026·2026-05-27
PS Seasoning non-fat dry milk made with recalled milk powder
PS Seasoning & Spices Non Fat Dry Milk in 1 lb packs is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Product
Non Fat Dry Milk 1#, Part #: 02000014P. Net Wt 1 lb (453g) PS Seasoning & Spices 216 W Pleasant St Iron Ridge, WI 53035.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0814-2026·2026-05-27
Ellsworth sour cream and onion seasoning made with recalled milk powder
Ellsworth Sour Cream + Onion Seasoning from PS Seasoning is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Product
Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0817-2026·2026-05-27
Blackstone parmesan ranch seasoning made with recalled milk powder
Blackstone Parmesan Ranch Seasoning in 7.3 oz containers is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Product
Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz (207g). UPC 7 17604-04106 2. Manufactured for North Atlantic Imports, LLC, Logan, UT 84321.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0832-2026·2026-05-27
Southern Style Nuts hunter mix jars recalled over potential Salmonella
Southern Style Nuts Hunter Mix in 30 oz plastic jars is being recalled over the potential presence of Salmonella. 30,515 cases are affected.
Product
Southern Style Nuts Hunter Mix 30 oz plastic jar UPC 085839916302, 4 jars per case
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·26V344000·2026-05-27
Ford Expedition and Lincoln Navigator seat belts may lock inadvertently
Ford is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles because the front seat belt pretensioner may inadvertently lock the belt so it cannot retract or extend.
Product
FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0836-2026·2026-05-27
Fisher Tex Mex Trail Mix recalled over potential Salmonella presence
Fisher Tex Mex Trail Mix in 30 oz plastic jars is being recalled over the potential presence of Salmonella. 606 cases are affected.
Product
Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941, 6 jars per case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0544-2026·2026-05-27
Erythromycin Tablets Recalled for Impurity Above Acceptable Limits
Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.
Product
ERYTHROMYCIN — ERYTHROMYCIN (ERYTHROMYCIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2202-2026·2026-05-27
Swan-Ganz Catheters Models 131F7 Through AIQSGF8 Recalled Nationwide
Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.
Product
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0815-2026·2026-05-27
PS Seasoning original smokehouse unit made with recalled milk powder
PS Seasoning 1P Original Smokehouse Unit is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 5,375.6 lbs are affected.
Product
1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15.10 lbs (6.85kg). PS Seasoning & Spices 216W Pleasant St Iron Ridge, WI 53035.
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·26V343000·2026-05-27
Ford Explorer, Ranger and Bronco engines may fail during driving
Ford is recalling certain 2025-2026 Explorer, Ranger and Bronco vehicles because the engine may fail, resulting in a loss of drive power. 1,536 vehicles are affected.
Product
FORD — FORD BRONCO, RANGER, EXPLORER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0831-2026·2026-05-27
Southern Style Nuts gourmet hunter mix recalled over potential Salmonella
Southern Style Nuts Gourmet Hunter Mix in 23 oz and 36 oz plastic jars is being recalled over the potential presence of Salmonella. 33,176 cases and 22 displays are affected.
Product
Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC 085839071483. 23 oz 6 jars per case case and 96 jars per display. 36 oz 6 jars per case
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-0818-2026·2026-05-27
PS Seasoning Save A Lot bind made with recalled milk powder
PS Seasoning PSW21585 Save A Lot Bind 50# is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 992.5 lbs are affected.
Product
PSW21585 Save A Lot Bind 50#, Part #: 20009709. PS Seasoning & Spices 216 W Pleasant St Iron Ridge, WI 53035.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2216-2026·2026-05-27
Medtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94215T) due to a potential sterile barrier breach. The affected product is a cardiopulmonary bypass vascular catheter distributed worldwide.
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0546-2026·2026-05-27
CIMZIA injection recalled due to lack of sterility assurance
UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.
Product
CIMZIA — CIMZIA (CERTOLIZUMAB PEGOL)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V339000·2026-05-27
Ember Recalls 2026-2027 Touring Edition Trailers Due to Shock Bolt Issue
Ember is recalling 2026-2027 Touring Edition trailers because incorrectly tightened shock bolts may detach, creating a road hazard and increasing crash risk.
Product
EMBER — EMBER TOURING EDITION
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2214-2026·2026-05-27
Medtronic GUNDRY Retrograde Cannula Model 94113T sterile barrier recall
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.
Product
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0541-2026·2026-05-27
Liraglutide Injection Recalled Due to Particulate Matter in Cartridges
Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.
Product
LIRAGLUTIDE — LIRAGLUTIDE (LIRAGLUTIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0796-2026·2026-05-27
VitaminAlly FulviLife Complex recalled over manufacturing practice deviations
VitaminAlly FulviLife Complex oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
Product
FulviLife Complex. Dosage:2 tablespoons (30mL). Liquid. Packaging: Plastic Bottle. Net Volume:16 fl oz (480 ml). Firm Address: VitaminAlly LLC Chandler, AZ 85225.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2227-2026·2026-05-27
Azurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage
The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.
Product
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2229-2026·2026-05-27
Integris-Allura X-ray systems with degraded deaeration hoses recalled
Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.
Product
Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0808-2026·2026-05-27
VitaminAlly liposomal sleep spray recalled over manufacturing practice deviations
VitaminAlly Liposomal Sleep Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
Product
Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225
Category
Food
Distribution
Distributed nationwide
HighNHTSA·26V340000·2026-05-27
Ford Maverick and Bronco Sport Front Control Arm Ball Joint Detachment Recall
Ford is recalling certain 2021–2026 Bronco Sport and 2022–2026 Maverick vehicles due to potentially loose or improperly installed front lower control arm ball joints that could disconnect from the wheel knuckle, risking loss of vehicle control and crashes.
Product
FORD — FORD MAVERICK, BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0806-2026·2026-05-27
VitaminAlly liposomal D3 and B12 spray recalled over manufacturing deviations
VitaminAlly Liposomal D3+B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
Product
Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0799-2026·2026-05-27
VitaminAlly mens 50+ multivitamin drops recalled over manufacturing deviations
VitaminAlly Liposomal Mens 50+ Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Product
Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
Category
Food
Distribution
Distributed nationwide