State

US Virgin Islands product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22101–22125 of 73565

ModerateFDA (Drugs)·D-0374-2022·2022-01-26
Clobetasol Propionate Foam Recalled for CGMP Deviations
Ingenus Pharmaceuticals is recalling 45,173 cans of Clobetasol Propionate Foam, 0.05%, nationwide due to Current Good Manufacturing Practice (CGMP) deviations. This is a voluntary, FDA Class II recall.
Product
Clobetasol Propionate Foam, 0.05%, packaged in a) 50 g can (NDC 50742-304-50), and b) 100 g can (NDC 50742-304-01), Rx only, Manufactured for: Ingenus Pharmaceuticals, LLC, Orlando, FL 32839-6408.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0389-2022·2022-01-26
Physicians CARE Extra Strength Pain Reliever recalled for CGMP deviations
Medique Products is recalling Physicians CARE Extra Strength Pain Reliever tablets nationwide because they were not manufactured under Current Good Manufacturing Practices (CGMP), as determined by an FDA inspection.
Product
Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg, 250 mg, 65 mg, packaged as 100-count Tablets (50 Packets, 2 tablets each) per carton, Manufactured for: Acme United Corporation 55 Walls Dr, Fairfield, CT 06824, UPC 0 73577…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0385-2022·2022-01-26
CVS Health Allergy Relief D Tablets Recalled for Failed Dissolution
CVS Health Allergy Relief D Extended Release Tablets are being recalled because they failed to meet dissolution specifications. The recall affects 41,784 boxes distributed nationwide.
Product
CVS Health, Allergy Relief D, Fexofenadine HCl 60mg/Antihistamine Pseudoephedrine HCl 120mg/Nasal Decongestant, a) 20 Extended Release Tablets per box, UPC 050428436189, b) 30 Extended Release Tablets per box, UPC 050428290538, Distributed by CVS Pharmacy Inc., One CVS Drive…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0390-2022·2022-01-26
Medique Pain-Off Tablets Recalled for Manufacturing Practice Violations
Medique Products is recalling Medique Pain-Off tablets nationwide after an FDA inspection found the products were not manufactured under Current Good Manufacturing Practices.
Product
Medique Pain-Off (Acetaminophen 250 mg, Aspirin (NSAID*) 250 mg, Caffeine 65 mg) Tablets, packaged in 2-count Tablets per Unit Dose Packet, packaged as a) 200-count Tablets (100 x 2) Unit Dose packets per carton, UPC 3 47682 22847 7, Reorder #22847; b) 500-count Tablets (250 x…
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·22061·2022-01-26
Family Dollar Recalls Beach Loungers Due to Collapse Injury Hazard
Family Dollar is recalling about 800 beach lounge chairs that can collapse unexpectedly, risking finger entrapment in metal folding joints. The loungers were sold nationwide from January 2019 through September 2021.
Product
Beach Loungers
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0376-2022·2022-01-26
Clobazam Oral Suspension Recalled for Failed Stability Specifications
VistaPharm is recalling Clobazam Oral Suspension 2.5 mg/mL due to failed stability specifications. The recall affects 18,456 bottles distributed nationwide.
Product
Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-058-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0387-2022·2022-01-26
Lexette Topical Foam Recall Due to Dispensing Defects
Mayne Pharma is recalling Lexette (halobetasol propionate) Topical Foam 0.05% due to manufacturing defects that cause the product to either not dispense or dispense liquid instead of foam. The recall affects 17,113 canisters distributed nationwide.
Product
Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville, NC 27834, NDC 51862-604-50
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0384-2022·2022-01-26
QC Quality Choice Fexofenadine/Pseudoephedrine Tablets Recalled for Failed Dissolution
Dr. Reddy's Laboratories is recalling QC Quality Choice Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg Extended-Release Tablets nationwide due to failed dissolution specifications that may reduce the medication's effectiveness.
Product
QC QUALITY CHOICE, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets, USP, Allergy & Congestion, 10 Tablets per box, NDC 63868-729-10, Distributed by C.D.M.A., Inc., 43157 W 9 Mile Rd, Novi, MI 48375, Made in India.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0383-2022·2022-01-26
Equate Allergy Relief D Tablets Recalled for Failed Dissolution
Dr. Reddy's Laboratories is recalling Equate Allergy Relief D Extended-Release Tablets distributed by Walmart nationwide due to failed dissolution specifications. The recall affects 137,856 boxes across multiple lot numbers.
Product
equate, Allergy Relief D, Fexofenadine HCl 60mg/Antihistamine, Pseudoephedrine HCl 120mg/Nasal Decongestant Extended-Release Tablets USP, a) 20 Extended Release Tablets per box, NDC 49035-273-20, b) 30 Extended Release Tablets per box, NDC 49035-273-30, Distributed by: Walmart…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0507-2022·2022-01-26
Heel Snuggler devices recalled for labeling changes without FDA approval
Philips North America recalled approximately 2.5 million Heel Snuggler units because labeling was modified after FDA clearance without obtaining updated regulatory approval.
Product
Heel Snuggler, Reference # 989805603411 99047
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0382-2022·2022-01-26
Dr. Reddy's Fexofenadine/Pseudoephedrine Tablets Fail Dissolution Specification
Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg Extended-Release Tablets because the tablets failed to meet dissolution specifications, which may affect the drug's effectiveness.
Product
Dr. Reddys, Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets USP, a) 10 tablets per box, UPC 343598823355, b) 20 tablets per box, UPC 343598823140, c) 30 tablets per box, UPC 343598823317, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ…
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·22059·2022-01-26
DeWALT 18-inch Corded Chain Saws Recall for Unintended Operation
DeWALT is recalling about 8,500 DWCS600 18-inch corded chain saws because the tool can remain running when the switch is in the off position or turn on unexpectedly when plugged in, posing an injury hazard.
Product
DEWALT DWCS600, 18-inch corded chain saws
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0509-2022·2022-01-26
Medichoice Infant Heel Warmer recalled due to unapproved labeling changes
Philips is recalling 2,925,800 Medichoice Infant Heel Warmer units because labeling was modified beyond the scope of FDA clearance. The devices cannot be sold without new 510(k) approval.
Product
Medichoice Infant Heel Warmer, Reference # 989805643721 1079906
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0378-2022·2022-01-26
Wal-Fex D Allergy and Decongestant Tablets Recalled for Failed Dissolution
Dr. Reddy's Laboratories is recalling Wal-Fex D Extended Release Tablets nationwide due to failed dissolution specifications. The affected product combines fexofenadine (antihistamine) and pseudoephedrine (decongestant).
Product
FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI — FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI (FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0388-2022·2022-01-26
Drug Recall: Mucus Relief D Subpotent Tablets
Dr. Reddy's Laboratories is recalling Mucus Relief D (Guaifenesin Pseudoephedrine HCl ER Tablets) nationwide due to subpotency. The affected product was distributed to Walgreen Co. stores across the USA.
Product
Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0379-2022·2022-01-26
Rugby Antihistamine and Decongestant Tablets Recalled for Failed Dissolution
Dr. Reddy's Laboratories is recalling Rugby brand antihistamine and nasal decongestant tablets nationwide due to failed dissolution specifications. The affected product is NDC 0536-1242-07, Lot #AC2106452F with expiration date 3/31/2023.
Product
Rugby, Antihistamine and Nasal Decongestant, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets USP, 30 Tablets per box, NDC 0536-1242-07, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI, 49152, Made in India.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0380-2022·2022-01-26
Rite Aid Allergy & Congestion Tablets Fail Dissolution Specifications
Rite Aid Pharmacy is recalling Allergy & Congestion extended-release tablets because two lots failed to meet dissolution specifications. The affected product was distributed nationwide.
Product
Rite Aid Pharmacy, Allergy & Congestion, Fexofenadine HCl 60mg & Pseudoephedrine HCl 120mg, Extended Release Tablets USP, 20 Extended-Release Tablets per box, UPC 011822738873, Distributed by Rite Aid, 30 United Lane, Camp Hill, PA 17011, Made in India.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V029000·2022-01-25
Forest River Recalls Transit Buses Due to Fire Risk from Relay Module
Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.
Product
GLAVAL BUS — GLAVAL BUS, STARTRANS, STARCRAFT BUS COMMUTE, SENATOR II HD, ALLSTAR XLT, ALLSTAR XL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V030000·2022-01-25
2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather
Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S, RA1250S, RA1250
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V031000·2022-01-25
Kia Recalls Vehicles Due to Potential Air Bag Deactivation
Kia is recalling specific 2017-2019 models because a defect may prevent air bags from deploying in a crash.
Product
KIA — KIA FORTE KOUP, SOUL EV, SEDONA, SOUL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V028000·2022-01-24
Inland Empire Trailers Recalls 2021 Models Due to Axle Spindle Nut Issues
Inland Empire Trailers is recalling 50 units of 2021 trailers because improperly tightened axle spindle nuts may cause overheating and loss of control.
Product
INLAND EMPIRE TRAILERS — INLAND EMPIRE TRAILERS CUSTOM TRAILER, UTILITY/ DUMP TRAILER, FLAT DECK TRAILER, ENCLOSED TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V027000·2022-01-24
2022 Mitsubishi Outlander Recalled for Defective Fuel Pump
Mitsubishi is recalling certain 2022 Outlander vehicles because the fuel pump may fail due to incorrectly fused internal components. Fuel pump failure can cause engine stall, increasing the risk of a crash.
Product
MITSUBISHI — MITSUBISHI OUTLANDER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V023000·2022-01-21
BMW Recalls 2019-2020 K 1600 Motorcycles for Rear Suspension Defect
BMW is recalling 2019-2020 K 1600 GT, GTL, and B motorcycles because a rear suspension link strut may be insufficiently strong, potentially affecting stability and increasing crash risk.
Product
BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V024000·2022-01-21
Nissan Recalls 2014-2016 Rogue Vehicles for Electrical Fire Risk
Nissan is recalling 2014-2016 Rogue vehicles because water intrusion may corrode an electrical connector, increasing the risk of fire.
Product
NISSAN — NISSAN ROGUE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V025000·2022-01-21
Rosenbauer Fire Trucks Recalled for Rear Axle Drive Pinion Fracture Risk
Rosenbauer America is recalling 127 Commander, Warrior, and Avenger vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning.
Product
ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, AVENGER
Category
Vehicle
Distribution
Distributed nationwide