State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58376–58400 of 74005

SevereFDA (Devices)·Z-1628-2014·2014-05-28
Philips Recalls Lithium Ion Batteries for IntelliVue Patient Monitors
Philips Medical Systems is recalling specific lithium ion batteries for IntelliVue Patient Monitors because they may overheat, ignite, or explode after extended use.
Product
Lithium Ion Battery M4605A and M4607A for use with IntelliVue Patient Monitors. The monitor is used for monitoring and recording of, and to generate alarms for, multiple physiological parameters.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1639-2014·2014-05-28
Fresenius Recalls Naturalyte Liquid Bicarbonate Concentrate Due to Contamination
Fresenius Medical Care is recalling Naturalyte Liquid Bicarbonate Concentrate bottles due to potential contamination. The product is used in hemodialysis machines.
Product
Naturalyte Liquid Bicarbonate Concentrate, 6.4 Liter Bottle Part Number: 08-4000-LB The concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1624-2014·2014-05-28
Hospira Recalls T-U-R Y-Sets Due to Potential Sterile Package Seal Defect
Hospira is recalling specific T-U-R Y-Sets because the Tyvek cover may not be completely sealed, potentially compromising the sterile package.
Product
LATEX-FREE; T-U-R Y-Set; Nonvented Set for Transurethral Resection Procedures; 96 inch (244 cm); For Flexible Irrigation Container Systems; List No. 6543-01; single use; Hospira Product Usage: For use in transurethral resection procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1626-2014·2014-05-28
Hospira Recalls Large Bore Y-Irrigation Sets Due to Packaging Seal Defect
Hospira is recalling specific lots of Large Bore Y-Irrigation Sets because the Tyvek cover may not be completely sealed, potentially compromising the sterile package.
Product
LATEX-FREE; LARGE BORE Y-IRRIGATION SET; Nonvented Set; 100 inch (254 cm); For Flexible Irrigation Container Systems; List No. 6599-01; single use; Hospira Product Usage: For Use With Flexible Irrigation Container Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1640-2014·2014-05-28
GE Healthcare Recalls NeuroMuscular Transmission Modules for Inaccurate Readings
GE Healthcare is recalling 1,794 NeuroMuscular Transmission Modules because they may display inaccurate muscle relaxation levels when used with ElectroSensors.
Product
GE Healthcare, NeuroMuscular Transmission Module, E-NMT-01 Product Usage: The Datex-Ohmeda S/5TM E-NMT module is indicated for monitoring the relaxation of the patient and regional block stimulation for nerve location.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V302000·2014-05-28
Champion Bus Defender Recall for Defective Seat Belt Buckles
Champion Bus is recalling 2014 Defender shuttle buses because seat belt buckles may fail to release, hindering emergency egress.
Product
CHAMPION BUS — CHAMPION BUS DEFENDER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1627-2014·2014-05-28
Hospira Recalls Latex-Free 4-Lead T-U-R Irrigation Sets Due to Sealing Defect
Hospira Inc. is recalling 29,380 Latex-Free 4-Lead T-U-R Irrigation Sets because the Tyvek cover may not be completely sealed, potentially compromising sterility.
Product
LATEX-FREE; 4-LEAD T-U-R IRRIGATION SET; Nonvented Set for Transurethral Resection Procedures; 85 inch (216 cm); For Flexible Irrigation Container Systems; List No. 15239-01; Single Use; Hospira Product Usage: For Transurethral Resection Procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1647-2014·2014-05-28
Siemens Recalls Dimension Vista Cyclosporine Test Kits Due to Under-Recovery
Siemens Healthcare Diagnostics is recalling Dimension Vista CSA and CSAE test kits because they may under-recover cyclosporine levels when using Small Sample Containers.
Product
Dimension Vista¿ CSA and CSAE The Cyclosporine method is an in vitro diagnostic test for the quantitative measurement of cyclosporine A (CSA) in human whole blood on the Dimension Vista¿ System. Measurements of CSA are used as an aid in the management of heart, liver and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1651-2014·2014-05-28
Heraeus Kulzer Recalls Gluma Desensitizer Power Gel Due to Extrusion Risk
Heraeus Kulzer is recalling Gluma Desensitizer Power Gel because it may extrude all at once, causing irritation, burning, or blistering to patients or dental professionals.
Product
Gluma Desensitizer Power Gel Product Usage: Usage: This is a class 2 medical device. For reduction or elimination of pain in exposed cervical areas that do not require restoration. It is also used for alleviation or reduction of dentinal sensitivity after preparation of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1649-2014·2014-05-28
Medline Esmark Elastic Bandages Recalled for Sterilization Failure
Medline Industries is recalling 2,860 Esmark Elastic Bandages because they may not have been properly sterilized.
Product
Esmark Elastic Bandage (Sterile), 4" x 9'. Item DYNJ05116A, Individually wrapped, 20 bandages per case. Packaged by Medline Industries Inc. This product is used as an elastic bandage to support and compress a part of a patient's body. It is also used as a tourniquet to restrict…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14193·2014-05-28
Hamilton Beach Recalls Baby Food Makers Due to Small Parts Hazard
Hamilton Beach is recalling bébé brand baby food makers because a stainless steel pin can loosen and fall into food. No injuries have been reported.
Product
Baby food processor
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1344-2014·2014-05-28
SigmaPharm Recalls Liothyronine Sodium Tablets Due to Cross-Contamination
SigmaPharm is recalling four lots of Liothyronine Sodium Tablets 5 mcg due to potential cross-contamination with trace amounts of a previously manufactured product.
Product
LIOTHYRONINE SODIUM — LIOTHYRONINE SODIUM (LIOTHYRONINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1325-2014·2014-05-28
Teva Recalls Buprenorphine Hydrochloride Tablets Due to Impurity Test Failures
Teva Pharmaceuticals is recalling 53,452 bottles of 8 mg Buprenorphine Hydrochloride sublingual tablets because stability testing revealed high out-of-specification impurity levels.
Product
BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 8 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-5379-56, UPC 3 0093-5379-56 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1630-2014·2014-05-28
SCM True Air Technologies Recalls JK Bariatric Beds for Design Control Failures
SCM True Air Technologies is recalling 24 JK Bariatric Beds nationwide due to lack of design controls, missing Device Master Records, and unapproved vendors.
Product
JK Bariatric Beds, True Air Technologies, Inc.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1648-2014·2014-05-28
Ortho-Clinical VITROS TT4 Calibrator Recalled for Calibration Failures
Ortho-Clinical Diagnostics is recalling VITROS TT4 Calibrators due to potential calibration failures or low quality control results.
Product
VITROS TT4 Calibrator For the quantitative measurement of total thyroxine (T4) in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System to aid in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1625-2014·2014-05-28
Hospira Recalls Cystoscopy Sets Due to Potential Sterile Package Seal Defect
Hospira Inc. is recalling specific cystoscopy and irrigation sets because the Tyvek cover may not be completely sealed, potentially compromising the sterile package.
Product
LATEX-FREE; CYSTOSCOPY/IRRIGATION SET; Nonvented, 77 inch (195 cm) for Constant or Intermittent Bladder Irrigation; For Use with Flexible Irrigation Container System; List No. 6544-01; Hospira Product Usage: For Constant or Intermittent Bladder Irrigation
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1348-2014·2014-05-28
Forest Pharmaceuticals Recalls Bystolic Tablets for Dissolution Failures
Forest Pharmaceuticals is voluntarily recalling one lot of Bystolic (nebivolol hydrochloride) tablets because dissolution test results failed to meet specifications.
Product
BYSTOLIC — BYSTOLIC (NEBIVOLOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1632-2014·2014-05-28
SCM True Air Technologies Recalls MaXair Mattress Replacement Systems
SCM True Air Technologies is recalling 83 MaXair True Low Air Loss Mattress Replacement Systems due to design control and documentation deficiencies.
Product
MaXair True Low Air Loss Mattress Replacement System, True Air Technologies, Inc.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1623-2014·2014-05-28
Hospira Recalls Latex-Free Extension Sets Due to Packaging Seal Defect
Hospira is recalling specific latex-free extension sets because the Tyvek cover may not be completely sealed, potentially compromising the sterile package.
Product
LATEX-FREE; EXTENSION SET; For Bladder Irrigation or Urinary Drainage, Compatible with T-U-R FLOW-POUCH RESERVOIR, list 6542, 71 inch (180 cm) Nominal Length; List No. 4693-01; single use; Hospira Product Usage: Bladder irrigation or urinary drainage
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1622-2014·2014-05-28
Siemens syngo Imaging XS Software Recall Due to Data Deletion Risk
Siemens Medical Solutions is recalling 64 syngo Imaging XS systems because a software change may have caused the deletion of archived medical images.
Product
syngo Imaging XS Syngo Imaging XS is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo Imaging…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1629-2014·2014-05-28
Anspach Irrigation Clip 40 Recalled Due to Incorrect Assembly
The Anspach Effort, Inc. is recalling 150 Anspach Irrigation Clip 40 units because they were assembled with incorrect, smaller clips.
Product
Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a method of supplying controlled, cooling irrigation during cutting, shaping, and removal of bone, including bones of the skull and spine.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2014·2014-05-28
SCM True Air Technologies Recalls ECATS E 850 Bariatric Beds
SCM True Air Technologies is recalling 48 ECATS E 850 Bariatric Beds due to manufacturing documentation and vendor approval failures.
Product
ECATS E 850 Bariatric Bed, True Air Technologies, Inc.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1347-2014·2014-05-28
Oasis Tears Lubricant Eye Drops Recalled for Missing Bottle Labels
Oasis Medical Inc. is recalling 10,549 bottles of Oasis Tears Lubricant Eye Drops because the label on the immediate bottle is missing.
Product
Oasis TEARS, Lubricant Eye Drops, 10mL/0.3 fl. oz. Bottle, OTC Only. Distributed by: OASIS, OASIS Medical, Inc., Glendora, CA 91741. UPC: 8 54819 00002 3.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·14V281000·2014-05-27
Mitsubishi Recalls 2014 Lancer Models for Power Steering Tube Clearance Issue
Mitsubishi is recalling 2014 Lancer Evolution and Ralliart vehicles because insufficient clearance between the power steering tube and crossmember brace may cause fluid leaks, increasing crash and fire risks.
Product
MITSUBISHI — MITSUBISHI LANCER EVOLUTION, LANCER RALLIART
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V280000·2014-05-27
Lotus Recalls 2008-2011 Models Due to Oil Cooler Hose Defect
Lotus is recalling 860 Elise, Exige, and Evora vehicles because the oil cooler hose may detach, posing fire and crash risks.
Product
LOTUS — LOTUS EXIGE, ELISE, EVORA
Category
Vehicle
Distribution
Distributed nationwide