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.

21726–21750 of 73565

SevereFDA (Devices)·Z-0625-2022·2022-02-23
Arrow-Trerotola Dialysis Catheter Recalled for Tip Separation During Use
Arrow-Trerotola Over-The-Wire PTD catheters used in dialysis procedures are being recalled due to reports of tip separation during use. The FDA classified this as a Class I recall affecting 1,265 units worldwide.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0623-2022·2022-02-23
Arrow-Trerotola Thrombolytic Device Tip Separation During Use Recalled
Teleflex Medical is recalling Arrow-Trerotola PTD kits due to reports of tip separation during use. The affected device is used for declotting dialysis grafts and fistulae.
Product
Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0653-2022·2022-02-23
Smiths Medical Medfusion Syringe Infusion Pumps Recalled for Alarm System Failures
Smiths Medical is recalling certain Medfusion syringe infusion pumps due to intermittent alarm system failures that may occur during power-on self-tests outside the warranty period.
Product
Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion Pumps serviced during the same time period in which a main board was replaced using replacement main board part numbers G6000361, G6000435, G6001260, G6001560, G6001562 and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0642-2022·2022-02-23
Dental Resin Product Recalled Due to Non-Registered Manufacturing and Mislabeling
Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.
Product
FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0638-2022·2022-02-23
Endoscope Reprocessor Tubing Assembly Error May Reduce Disinfection Effectiveness
Olympus OER-Elite Endoscope Reprocessors may have incorrectly assembled detergent and alcohol tank tubing, causing solutions to be dispensed in reversed cycles. This results in ineffective endoscope disinfection and potential patient exposure to residual detergent.
Product
OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes, their accessories, and endoscope reprocessor accessories
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0640-2022·2022-02-23
Liko Mobile Patient Lifts Recalled for Missing Bushings and Wear Risk
Hill-Rom is recalling 1,215 Liko M220 and M230 mobile patient lifts with missing bushings that cause wear and risk of patient falls. Units were distributed worldwide.
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22087·2022-02-23
Bebe au Lait Wooden Teethers Recalled for Choking Hazard
Bebe au Lait is recalling approximately 8,600 wooden teethers because the string connecting beads can come untied, releasing beads that pose a choking hazard to young children. The company has received six reports of detached beads, including one case where a child placed a bead in their mouth.
Product
Wooden Teethers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V105000·2022-02-23
2022 Keystone Cougar Tires: Load Range Defect Increases Crash Risk
Keystone RV recalls 2022 Cougar trailers with incorrectly specified tires. Load Range D tires were installed instead of required Load Range E, creating overload and crash risk.
Product
KEYSTONE — KEYSTONE COUGAR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0639-2022·2022-02-23
Liko M220 mobile lifts recalled for missing bushing, fall risk
Hill-Rom is recalling 5,470 Liko M220 mobile lifts used in nursing homes due to a missing bushing that can cause wear and potentially lead to patient falls.
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22E013000·2022-02-23
Comoto Recalls Bilt Motorcycle Helmets for Impact Protection Defect
Comoto is recalling specific Bilt motorcycle helmets that may not adequately protect the wearer during a head impact, failing federal safety standards.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22086·2022-02-23
Festive Lights Hanukkah Menorahs Recalled Due to Fire Hazard
The TJX Companies is recalling about 7,900 Festive Lights Hanukkah Menorahs because the resin and MDF material can burn or catch fire when holding lit candles. Three incidents of burning or catching fire have been reported, with no injuries or property damage.
Product
Festive Lights Hanukkah Menorahs
Category
Consumer Product
Distribution
Distributed nationwide
ModerateNHTSA·22V102000·2022-02-23
Audi Recalls 2022 RS 5 Models for Incorrect Tire Loading Label
Audi is recalling 2022 RS 5 vehicles because the B-pillar tire and loading label displays an incorrect maximum weight, which may lead to vehicle overload.
Product
AUDI — AUDI RS 5
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0565-2022·2022-02-23
Alprazolam Tablets 0.5 mg Recalled Due to cGMP Deviations
ANI Pharmaceuticals is voluntarily recalling Alprazolam Tablets USP 0.5 mg in multiple package sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 205,662 bottles distributed across the United States.
Product
Alprazolam Tablets, USP 0.5 mg, packaged in a) 100-count bottles (NDC 67253-901-10), b) 500-count bottles (NDC 67253-901-50), and c) 1000-count bottles (NDC 67253-901-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0560-2022·2022-02-23
Moxifloxacin Ophthalmic Solution Recall for Failed Impurities Specifications
Aurobindo Pharma USA Inc. is recalling Moxifloxacin Ophthalmic Solution 0.5% due to failed impurities and degradation specifications. The recall affects 115,776 bottles distributed nationwide.
Product
MOXIFLOXACIN — MOXIFLOXACIN (MOXIFLOXACIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0568-2022·2022-02-23
Pyrazinamide Tablets 500 mg Recalled Due to cGMP Deviations
ANI Pharmaceuticals, Inc. has recalled Pyrazinamide Tablets USP 500 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 5,477 bottles distributed nationwide.
Product
Pyrazinamide Tablets, USP 500 mg, 100-count bottles, Rx only, Manufactured by: ULTRAtab Laboratories, Inc. Highland, NY 12528, Distributed by Par Pharmaceuticals, Chestnut Ridge, NY 10977, NDC 67253-660-10.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0566-2022·2022-02-23
Alprazolam Tablets USP 1.0 mg Recalled for cGMP Deviations
ANI Pharmaceuticals has recalled Alprazolam Tablets USP 1.0 mg distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 173,499 bottles across multiple lot numbers.
Product
Alprazolam Tablets, USP 1.0 mg, packaged in a) 100-count bottles (NDC 67253-902-10), b) 500-count bottles (NDC 67253-902-50), and c) 1000-count bottles (NDC 67253-902-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0558-2022·2022-02-23
Diazepam Oral Solution Recalled for Failed Impurity Specifications
Lannett Company is recalling Diazepam Oral Solution (Concentrate) 5 mg/mL due to out-of-specification results for related substances, indicating failed impurities and degradation testing.
Product
Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1768-36.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0643-2022·2022-02-23
Dental Resins Recalled for Manufacturing Facility and Origin Labeling Violations
Envisiontec US LLC recalled 795 units of FLEXCERA SMILE dental resins manufactured between April 2021 and September 2021 because they were produced in a non-FDA-registered facility and falsely labeled as German origin.
Product
FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0578-2022·2022-02-23
Chlorthalidone Tablets Recalled for Foreign Matter Contamination
Sun Pharmaceutical is recalling Chlorthalidone Tablets USP 25 mg (Lot #P0602, expiration 03/2023) due to stainless steel microscopic wear particles, punch lubricant oil, and silicone particles from the dust cup found in the product.
Product
CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0564-2022·2022-02-23
Alprazolam Tablets USP 0.25 mg Recalled for cGMP Deviations
ANI Pharmaceuticals is recalling Alprazolam Tablets USP 0.25 mg nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects multiple lot numbers of 100-count, 500-count, and 1000-count bottles distributed across the United States.
Product
Alprazolam Tablets, USP 0.25 mg, packaged in a) 100-count bottles (NDC 67253-900-10), b) 500-count bottles (NDC 67253-900-50), and c) 1000-count bottles (NDC 67253-900-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0567-2022·2022-02-23
Alprazolam Tablets 2.0 mg Recalled for cGMP Deviations
ANI Pharmaceuticals is recalling Alprazolam Tablets, USP 2.0 mg nationwide due to current good manufacturing practice (cGMP) deviations. The recall affects approximately 70,788 bottles distributed throughout the United States.
Product
Alprazolam Tablets, USP 2.0 mg, packaged in a) 100-count bottles (NDC 67253-903-10), b) 500-count bottles (NDC 67253-903-50), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0716-2022·2022-02-23
Erythromycin Topical Gel Recalled for Failed Impurity Specifications
Teligent Pharma is recalling one lot of Erythromycin Topical Gel USP 2% because the product failed to meet specifications for unknown maximum related compounds.
Product
Erythromycin Topical Gel USP, 2%, Net Wt 30 g tube, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation, dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-053-66.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0641-2022·2022-02-23
Microbiology quality control kit recalled for incorrect inner label
A KWIK-STIK quality control kit has an incorrect inner label. The product contains Campylobacter coli, but the inner label states Haemophilus influenzae.
Product
KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V100000·2022-02-22
2021 Porsche Taycan: Center Seat Belt Buckle May Block Child Seat Anchors
Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E012000·2022-02-22
Comoto Recalls Street & Steel Raider Motorcycle Helmets for Impact Protection Defect
Comoto is recalling Street & Steel Raider motorcycle helmets because they may not adequately protect the wearer in a crash, increasing the risk of injury.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide