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.

21001–21025 of 73565

HighFDA (Drugs)·D-0777-2022·2022-04-27
Ipamorelin and Sermorelin Injectable Medications Recalled Due to Sterility Deviations
North American Custom Laboratories is recalling 189 vials of Ipamorelin/Sermorelin injectable due to manufacturing deviations that call into question the sterility of this prescription medication.
Product
Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL (10 mL) Injection, 10 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V280000·2022-04-27
Micro Bird Recalls School Buses Due to Insufficient Seat Hardware
Micro Bird is recalling 2018-2020 MB II school buses because GenQ seats may be attached with insufficient hardware, increasing injury risk in a crash.
Product
MICRO BIRD — MICRO BIRD MB II SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-04272022-01·2022-04-27
USDA Issues Public Health Alert for Ground Beef Due to E. coli O26
USDA FSIS issued a public health alert for specific ground beef products produced in December 2021 due to possible E. coli O26 contamination. Consumers are advised to discard or return the affected items.
Product
FSIS Issues Public Health Alert for Ground Beef Products Due to Possible E. coli O26 Contamination
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0979-2022·2022-04-27
Siemens Artis Q.zen ceiling system recall: inadequate X-ray tube cooling risk
Siemens recalls 81 Artis Q.zen ceiling imaging systems distributed nationwide due to risk of inadequate X-ray tube cooling if coolant levels fall below a critical threshold, potentially triggering system shutdown.
Product
Artis Q.zen ceiling, Model Number 10848354
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0964-2022·2022-04-27
Merlin PCS 3650 Programmer May Fail to Terminate Pacing Test Properly
A software anomaly in the Merlin PCS 3650 programmer may cause an in-clinic pacing test to fail terminating and prevent restoration of the implanted device's normal settings. Approximately 30,069 affected devices have been distributed worldwide.
Product
Merlin PCS 3650 programmer Model 3330 software
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V283000·2022-04-27
School buses missing warning label for inoperative collision mitigation system
Navistar is recalling certain 2022-2023 IC BUS school buses because the warning label for the inoperative collision mitigation system may be missing. Drivers may not be aware the safety system is not functioning.
Product
IC BUS — IC BUS RESB, CESB
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0970-2022·2022-04-27
Siemens Artis zee biplane X-ray system cooling defect recall
Siemens is recalling 373 Artis zee biplane X-ray diagnostic systems due to a cooling circuit defect that could prevent adequate tube cooling. When the coolant level drops, the system may overheat and shut down imaging capabilities.
Product
Artis zee biplane, Model Number 10094141
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0983-2022·2022-04-27
GE Healthcare MRI Systems May Fall During De-Installation Without Proper Rigging
GE Healthcare MRI systems may fall during magnet de-installation if rigging and hardware are not properly installed and secured, creating a potential injury hazard.
Product
GE Healthcare MR Systems, Magnetic Resonance imaging (MRI). SIGNA Premier, SIGNA Architect, SIGNA Pioneer, Discovery MR750w 3.0T, Discovery MR750 3.0T, SIGNA PET/MR, 1.5T SIGNA Creator, 1.5T SIGNA Explorer, 1.5T SIGNA MR355, 1.5T SIGNA MR360, 1.49T SIGNA MR380, SIGNA Voyager…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0990-2022·2022-04-27
Gallant HF Implantable Cardioverter Defibrillator Bluetooth Malfunction Impairs Remote Monitoring
The Gallant HF Implantable Cardioverter Defibrillator (REF# CDHFA500Q) may experience a Bluetooth malfunction that prevents remote monitoring and reduces battery life. Consult your healthcare provider.
Product
Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0776-2022·2022-04-27
Injectable Drug Recalled for Sterility Concerns Due to Manufacturing Defects
North American Custom Laboratories recalls BPC-157 injectable solution due to manufacturing deviations that compromise sterility assurance. The FDA classified this as a Class II recall affecting 778 vials distributed nationwide.
Product
BPC-157 2 mg/mL (5 mL) Injection, 5 mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0954-2022·2022-04-27
Medical Device Reference Standard Recalled for Inadequate Quality Control Process
Microbiologics Inc recalls an inactivated Mycoplasma genitalium reference standard (Lot HE0069-02-1) because its quality control process did not meet specification requirements. This reference material is used in diagnostic and laboratory testing.
Product
Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0971-2022·2022-04-27
X-Ray Imaging System Cooling Circuit Failure Recall
Siemens is recalling Artis zee floor MN X-ray systems due to a potential cooling circuit malfunction. If coolant drops below adequate levels, the X-ray tube may not cool properly and the system will automatically shut down.
Product
Artis zee floor MN, Model Number 10094142
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0955-2022·2022-04-27
Inactivated Mycoplasma genitalium reference material recalled due to inadequate QC
Microbiologics Inc is recalling an inactivated Mycoplasma genitalium reference material (Catalog # HE0070N, Lot HE0070-01-1) because the quality control process did not meet specification requirements.
Product
Inactivated macrolide-resistant Mycoplasma genitalium
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0784-2022·2022-04-27
Hand Sanitizer Recalled Over Manufacturing Quality Deviations
VIRGIN SCENT INC has recalled 46,368 bottles of artnaturals Hand Sanitizer nationwide due to manufacturing process deviations. The affected lots were produced using common ingredients from a contaminated batch.
Product
artnaturals Hand Sanitizer
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0956-2022·2022-04-27
Abbott TactiCath Ablation Catheter Disabled by Preprogrammed First-Use Date
Abbott is recalling 2,134 TactiCath ablation catheters manufactured with a preprogrammed 'First Use Date' that disables the device. Affected devices with 37 specific lot numbers were distributed in the U.S. and 21 other countries.
Product
Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve D-F, Model A-TCSE-DF, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0948-2022·2022-04-27
Baxter Syringe Tip Caps Recalled Due to Incorrect Labeling
Baxter is recalling DISCPAC syringe tip caps that are mislabeled as self-righting when they do not possess this capability, risking improper use in medical procedures.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0949-2022·2022-04-27
Terumo Cardiovascular Procedure Kit Recall for Shipping Damage
Terumo Cardiovascular Systems Corp is recalling two lots of cardiovascular procedure kits due to packaging damage that occurred during shipping. The recall affects 64 units distributed in California and Indiana.
Product
Cardiovascular Procedure Kit catalog # 76645 & 73806
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0773-2022·2022-04-27
Diclofenac Sodium Topical Solution Recalled Due to Manufacturing Quality Deviations
Preferred Pharmaceuticals, Inc. is recalling Diclofenac Sodium Topical Solution because the manufacturing firm discontinued its stability study program, a CGMP violation. All products within their expiration dates are affected.
Product
Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred Pharmaceuticals, Inc., The Physicians Solutions, NDC 68788-7918-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0968-2022·2022-04-27
X-ray Imaging System Cooling Failure May Cause Tube Overheating
Siemens Artis zee ceiling X-ray systems may fail to cool the X-ray tube if the coolant level drops. The system will automatically block X-ray emissions and display warning messages to prevent equipment damage.
Product
Artis zee ceiling, Model Number 10094137
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0984-2022·2022-04-27
Beckman Coulter IRISpec CA Control glucose measurement failures recalled
Beckman Coulter is recalling IRISpec CA/CB/CC control kits due to failures in glucose measurement for the CA Control component. The recall affects laboratory quality control products distributed worldwide.
Product
Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100 mL bottles each of CA Control, CB Control, and CC Control.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0783-2022·2022-04-27
FDA Recalls artnaturals Scent-Free Hand Sanitizer for Manufacturing Deviations
artnaturals Scent-Free Hand Sanitizer is recalled due to manufacturing process deviations. Approximately 570,268 bottles distributed nationwide are affected.
Product
artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0981-2022·2022-04-27
Oral DNA Collection Device Recalled for Evaporating Stabilizing Liquid
DNA Genotek Inc. is recalling ORAcollect Dx oral DNA collection devices because the stabilizing liquid can evaporate, reducing shelf life and potentially affecting sample preservation.
Product
ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012, OCD-100.014+ACP078, OCD-100.014+ACP078, OCD-100.032 and OCD-100A, OCD-100A.022, OCD-100A.023, OCD-100A.024, OCD-100A.025
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0980-2022·2022-04-27
Artis Q.zen Biplane X-ray Systems Coolant Level Failure Recall
Siemens is recalling 69 Artis Q.zen biplane systems where coolant levels may drop sufficiently to prevent adequate X-ray tube cooling, triggering automatic shutdown safeguards.
Product
Artis Q.zen biplane, Model Number 10848355
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0982-2022·2022-04-27
Oral RNA Collection Kit Recalled Due to Stabilizer Evaporation
DNA Genotek Inc. is recalling ORAcollect RNA: ORE-100 kits due to evaporation of the stabilizing liquid, which reduces shelf life. Approximately 17,080 units are affected, including lot YJ530.
Product
ORAcollect RNA: ORE-100
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V278000·2022-04-26
Porsche Taycan seat wire harness defect may deactivate airbags
Porsche is recalling certain 2020-2021 Taycan vehicles because the driver and passenger seat wire harness could become damaged during horizontal seat adjustment. A damaged harness may deactivate airbags, increasing crash injury risk.
Product
PORSCHE — PORSCHE TAYCAN
Category
Vehicle
Distribution
Distributed nationwide