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.

58426–58450 of 74005

SevereFDA (Devices)·Z-1567-2014·2014-05-21
CareFusion Recalls Alaris Pump 8100 Due to Software Delay Issue
CareFusion is recalling Alaris Pump model 8100 units with specific software versions because a defect may prevent the pump from properly delaying infusions.
Product
Alaris Pump model 8100 with software version 9.1.18 and software upgrade kits with "Delay Until" Option and "Multidose" Feature The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1612-2014·2014-05-21
Medline Mucus Specimen Traps Recalled for Potential Sterility Issues
Medline Industries is recalling 1,610 mucus specimen traps because they may not be sterile, which could contaminate patient specimens.
Product
Mucus Specimen Trap 40 cc, Specimen Trap 40 cc with additional transport cap; Product number DYND44140 (pack of 50), Product number DYND44140H (individual). Mucus Specimen Trap 80 cc, Specimen Trap 80 cc w/ additional transport cap; Product number DYND44180 (pack of 50).…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1616-2014·2014-05-21
Roche Recalls ACCU-CHEK Compact Plus Test Strips Due to Ceftriaxone Interference
Roche is recalling ACCU-CHEK Compact Plus test strips because they may produce erroneously low blood glucose readings in patients taking Ceftriaxone.
Product
ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus Meters; 17 count sample strip 51 count retail strip; 102 count retail strip; 51 count MedBen strip 51 count Mail Order strip; Sample Kit 16 per case. The ACCU-CHEK Compact Plus Test Strips are for use…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2014·2014-05-21
Zimmer Recalls Neoprene Tennis Elbow Supports Due to Latex Contamination
Zimmer, Inc. is recalling 649 units of Neoprene Tennis Elbow Supports because raw material labeled as latex-free actually contained latex.
Product
Tennis Elbow Support, Neoprene***LATEX FREE" Product Usage: Provides compression and warmth for mild to moderate elbow strains and sprains.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1615-2014·2014-05-21
Biomet ExploR Radial Stem Recalled for Missing Threads
Biomet is recalling eight ExploR 7x26mm Modular Radial Stem implants because missing wedge ramp threads may cause set screw loosening, potentially requiring revision surgery.
Product
ExploR 7x26mm Modular Radial Stem, Catalog number 11-210062. Elbow prosthesis orthopedic implant.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1605-2014·2014-05-21
Zimmer Hinged Knee Support Recalled Due to Latex Contamination
Zimmer, Inc. is recalling 546 units of Hinged Knee Supports because raw material labeled as latex-free actually contained latex.
Product
Hinged Knee Support***LATEX FREE" Product Usage: Provide added lateral stability and allows the knee to tolerate more strenuous activity during recuperation.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14187·2014-05-21
Nest Labs Recalls Nest Protect Smoke and Carbon Monoxide Alarms
Nest Labs is recalling Nest Protect Smoke + CO alarms because the Nest Wave feature can prevent the alarm from sounding during a fire. No injuries or property damage have been reported.
Product
Nest Protect: Smoke + CO Alarm
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1604-2014·2014-05-21
Zimmer Cartilage Knee Brace Recalled Due to Latex Contamination
Zimmer, Inc. is recalling 2,222 units of Cartilage Knee Braces because raw material labeled as latex-free actually contained latex.
Product
Cartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment and support of many types of knee injuries or following surgical and nonsurgical correction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1613-2014·2014-05-21
Siemens Syngo Dynamics PACS Recalled for Patient Demographics Display Error
Siemens Medical Solutions is recalling 50 Syngo Dynamics v9.5 systems due to a software error that may cause incorrect patient demographics to be displayed.
Product
Syngo Dynamics v9.5 system. A Picture Archiving and Communication System (PACS) intended for acceptance, transfer, display, storage, archive and manipulation of digital medical images, including quantification and report generation.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V268000·2014-05-21
Stoughton Trailers Recall 2014 Models for Suspension Pivot Bolt Failure
Stoughton is recalling 879 specific 2014 trailers because suspension pivot bolts may fail, potentially causing the axle to separate and increasing crash risk.
Product
STOUGHTON — STOUGHTON AVW, ZGPVW, AHV, AVXW
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V269000·2014-05-21
Eldorado Aerotech 240 Recalled for Wheelchair Lift Cable Fire Risk
Eldorado is recalling 2012-2014 Aerotech 240 vehicles because a wheelchair lift cable may not clear the lift, potentially causing a short circuit and fire.
Product
ELDORADO — ELDORADO AEROTECH 240
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1618-2014·2014-05-21
Fresenius Hemodialysis Machines Recalled for Potential UF Pump Detection Failure
Fresenius Medical Care is recalling 79 hemodialysis machines and replacement parts because they may fail to detect a disconnected Ultrafiltration (UF) Pump.
Product
Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards and also sold as replacement parts for use with Fresenius 2008-Series Hemodialysis Machines (2008K, 2008K2, 2008K@home and 2008T). Part Number: 190234 Revision K
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1603-2014·2014-05-21
Zimmer Drop Lok Knee Brace Recalled Due to Latex Contamination
Zimmer, Inc. is recalling Drop Lok Knee Braces because raw material labeled as latex-free was found to contain latex. The recall affects 131 units distributed in the US and internationally.
Product
DROP LOK" Knee Brace***LATEX FREE" Product Usage: Used in the treatment, support, and rehabilitation of many types of knee injuries or following surgical correction.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D1292-2014·2014-05-21
Teva Recalls Methyldopa Tablets Due to Manufacturing Deviations
Teva Pharmaceuticals USA is recalling Methyldopa Tablets USP, 500 mg, due to CGMP deviations and laboratory testing not following GMP requirements.
Product
METHYLDOPA Tablets USP, 500 mg, 100 count bottle, Rx only, Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-2932-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1610-2014·2014-05-21
Ortho Development Recalls PS-C Femoral Knee Implant Components
Ortho Development Corporation is recalling five PS-C Femoral Nonporous Rt Sz 6 knee implant components because pegged versions were found in boxes labeled for the pegless version.
Product
PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision System, for total knee arthroplasty procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2014·2014-05-21
Mindray DPM 6 Patient Monitor Recalled for Uncleared ST/Arrhythmia Feature
Mindray DS USA is recalling four DPM 6 patient monitors in Ohio because the included Multi Parameter Module contains a cardiac ST/Arrhythmia analysis feature that is not cleared for marketing.
Product
DPM 6 Monitor in use with a Multi Parameter Module (MPM). Patient monitor used for monitoring, displaying, reviewing, storing, and alarming of multiple physiological parameters including ECG, arrhythmia detection, ST segment analysis, heart rate (HR), respiration rate (RESP)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1614-2014·2014-05-21
Greatbatch Recalls Coaxial Micro-Introducer Kits Due to Shelf Life Documentation Issues
Greatbatch Medical is recalling Coaxial Micro-Introducer Kits because documentation does not support the claimed five-year shelf life.
Product
Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems Order Number/Part Description 10636-001 8004011 Kit Coax 10 Pack 4FR Bard 10636-002 8005011 Kit Coax 10 Pack 5FR Bard 10636-007 8004012 Kit Coax 10 Pack 4FR Bard 10636-008 8005012 Kit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1574-2014·2014-05-21
Anspach Cutting Bur Recall Due to Incorrect Product Code Labeling
The Anspach Effort, Inc. is recalling 30 Anspach Cutting Burs (REF L-3SD) because the product code S-3SD was included, which is shorter than the labeled product.
Product
ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length. REF L-3SD Use with LONG Attachments. Used for cutting and shaping bone, including the spine and cranium.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1323-2014·2014-05-21
First Aid Only Recalls Ibuprofen Dispenser Boxes Containing Aspirin
First Aid Only is recalling Smart Tab First Aid ezRefill System Ibuprofen boxes that were accidentally filled with aspirin packs.
Product
Smart Tab First Aid ezRefill System Ibuprofen dispenser boxes (Item Number FAE 7014), 20 count boxes, First Aid Only Inc., Vancouver, WA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1316-2014·2014-05-21
Flawless Beauty LLC Recalls Laroscorbine Platinium Injectable Solution
Flawless Beauty LLC is recalling Laroscorbine Platinium injectable solution because it was marketed without an approved NDA/ANDA and includes drug claims to act as an antidote.
Product
Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution, 1 gm/0.35 gm, 5 mL ampoules, packaged in 10-count ampoules per box, Laboratories Roche Nicholas S.A., F-74240 Gaillard, - Tel.: 04 50 87 70 70, Fabricant : Produits Roche, 52, Bld du Parc, 92521 Neulilly…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1617-2014·2014-05-21
McKesson Radiology-PACS software recall for missing high-priority alert icon
McKesson Medical Imaging is recalling 45 units of McKesson Radiology-PACS software because the high-priority alert icon was not displayed when no Stat studies were present.
Product
McKesson Radiology-PACS. McKesson Radiology is a medical image and information application that is intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from various medical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1294-2014·2014-05-21
Teva Recalls Indomethacin Capsules Due to Manufacturing Quality Deviations
Teva Pharmaceuticals USA is recalling 7,694 bottles of Indomethacin Capsules USP, 25 mg, due to CGMP deviations and laboratory testing failures.
Product
INDOMETHACIN Capsules USP, 25 mg 100 count bottle, Rx only , Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-4029-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1295-2014·2014-05-21
Teva Recalls Indomethacin Capsules Due to Manufacturing Quality Deviations
Teva Pharmaceuticals USA is recalling Indomethacin Capsules USP, 50 mg, because laboratory testing was not conducted in accordance with Good Manufacturing Practice (GMP) requirements.
Product
INDOMETHACIN Capsules USP, 50 mg, a) 100 count bottle, (NDC 0093-4030-01), b) 500 count bottle, (NDC 0093-4030-05), Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1293-2014·2014-05-21
Teva Recalls Glyburide and Metformin Tablets Due to GMP Deviations
Teva Pharmaceuticals USA is recalling specific bottles of Glyburide and Metformin Hydrochloride tablets due to laboratory testing deviations from GMP requirements.
Product
GLYBURIDE and METFORMIN HYDROCHLORIDE Tablets USP, 5mg/500mg, 500 count bottle, Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC: 0093-5712-05
Category
Drug
Distribution
Distributed nationwide
CriticalCPSC·14185·2014-05-20
Bed Handles Inc. Recalls Portable Bed Handles Due to Entrapment Deaths
Bed Handles Inc. is recalling about 113,000 portable bed handles sold without safety retention straps. Three deaths were reported after users became entrapped between the mattress and the shifting handles.
Product
Portable bed handles
Category
Consumer Product
Distribution
Distributed nationwide