State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59576–59600 of 74011

SevereFDA (Drugs)·D-1038-2014·2014-02-05
Mentholatum Recalls Rohto Eye Drops Due to Sterility Concerns
The Mentholatum Company is recalling Rohto eye drops because of concerns about the quality assurance of sterility controls.
Product
ROHTO Redness Relief, ice, Redness Reliever, Lubricant, Astringent Eye Drops, Sterile, Net. Wt. 0.4 FL OZ (13 mL). UPC 3 10742 01086 2, Manufactured by Rohto-Mentholatum (Vietnam) Co., Ltd. for The Mentholatum Company, Orchard Park, NY 14127. Made in Vietnam.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0862-2014·2014-02-05
Codman Certas Programmable Valves Recalled for Potential Malfunction
Codman & Shurtleff is recalling 369 Certas Programmable Valves used for hydrocephalus because they may not operate properly.
Product
Codman Certas Programmable Valve In Line Valve with SiphonGuard Device, Catheter and Accessories Product Code: 82-8805 Product Usage: The CODMAN CERTAS Programmable Valve is an implantable device that provides constant intraventricular pressure and drainage of CSF…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0860-2014·2014-02-05
Codman Certas Programmable Valves Recalled for Potential Malfunction
Codman & Shurtleff, Inc. is recalling 431 Codman Certas Programmable Valves because they may not operate properly. These implantable devices are used to manage hydrocephalus.
Product
Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal Catheter and Accessories Product Code: 82-8803 Product Usage: The CODMAN CERTAS Programmable Valve is an implantable device that provides constant intraventricular pressure and drainage of CSF…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1035-2014·2014-02-05
Hospira Recalls Aminosyn 3.5% Bags Due to Sterility Concerns
Hospira Inc. is recalling 15,258 bags of Aminosyn 3.5% M Sulfite-Free due to a lack of assurance of sterility and potential leakage from the administrative port.
Product
Aminosyn 3.5% M Sulfite-Free, A Crystalline Amino Acid Solution* with Maintenance Electrolytes with Phosphorus, 1000 mL bag, Rx only. Hospira Inc, Lake Forest, IL, 60045. NDC: 0409-4196-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1036-2014·2014-02-05
Hospira Recalls Heparin Sodium Bags Due to Sterility Concerns
Hospira is recalling 27,780 bags of Heparin Sodium 2000 USP Units per 1000 mL due to a lack of assurance of sterility and potential leakage from the administrative port.
Product
HEPARIN SODIUM — HEPARIN SODIUM (HEPARIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0835-2014·2014-02-05
DeRoyal Aquarius Hot/Cold Therapy Unit Recalled for Temperature Control Failure
DeRoyal Industries is recalling 121 Aquarius Hot/Cold Therapy Combo Units because they fail to monitor water temperature, posing a risk of temperature injuries and electric shock.
Product
DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit, w/ Knee/Shoulder Blanket NS, REF T652NS, Rx only, Manufacturer DeRoyal Industries, Inc. 200 DeBusk Lane, Powell, TN 37849. Physical Therapy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0885-2014·2014-02-05
Synergetics Recalls 25ga Endo Illuminator Due to Faulty Seals
Synergetics Inc is recalling 96 units of 25ga Endo Illuminator devices because faulty seals on the outer pouch could fail, potentially compromising sterility.
Product
25ga Endo Illuminator, Synergetics, inc., length 7.0 ft, sterile / EO, 56.02.25 Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2014·2014-02-05
Synergetics Recalls 25ga Aspirating Endo Illuminator Due to Seal Failure
Synergetics is recalling 25ga Aspirating Endo Illuminators because faulty seals on the outer pouch could fail, compromising the sterile status of the ophthalmic devices.
Product
25ga Aspirating Endo Illuminator, Synergetics, length 7.5 ft, sterile / EO, 56.24.25P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0877-2014·2014-02-05
Synergetics Recalls 25ga Awh Chandelier Due to Faulty Sterile Seals
Synergetics Inc. is recalling 36 units of 25ga Awh Chandeliers because faulty seals on the outer pouch could fail, compromising the sterile status of the ophthalmic devices.
Product
25ga Awh Chandelier, Synergetics, inc., length 8.0 ft, sterile / EO, 56.50.25P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0886-2014·2014-02-05
Synergetics Recalls Stiff 25ga Endo Illuminator Due to Faulty Seals
Synergetics Inc is recalling 48 units of Stiff 25ga Endo Illuminators because faulty seals on the outer pouch could result in seal failure.
Product
Stiff 25ga Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.02.25PS. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0888-2014·2014-02-05
Synergetics Recalls Corona Shielded Wide Field Endo Illuminator Due to Seal Failure
Synergetics Inc. is recalling specific lots of Corona Shielded Wide Field Endo Illuminators because faulty seals on the outer pouch could fail, compromising sterility.
Product
"The Corona" Shielded Wide Field Endo Illuminator, Synergetics, inc. 20ga, length 7.0 ft, sterile / EO, 56.12. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1435-2014·2014-02-05
Lambs Farm Banana Nut Bread Recalled for Undeclared Soy Allergen
The Lambs Farm, Inc. is recalling Banana Nut Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.
Product
Banana Nut Bread loaf sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 8 oz. This product was only sold as a part of the Bread Trio gift box.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0878-2014·2014-02-05
Synergetics Recalls 29ga Ophthalmic Chandeliers Due to Faulty Seals
Synergetics Inc. is recalling 233 units of 29ga Oshima Dual Chandeliers because faulty seals on the outer pouch could fail, compromising the sterile status of the devices.
Product
29ga Oshima Dual Chandelier, Synergetics, inc., length 7.5 ft, sterile / EO, 56.50.29P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0894-2014·2014-02-05
Synergetics Recalls 23ga Wide Field Endo Illuminator Due to Seal Failure
Synergetics Inc is recalling 568 units of 23ga Wide Field Endo Illuminators because faulty seals on the outer pouch could result in seal failure.
Product
23ga Wide Field Endo Illuminator, Synergetics, inc., length 7.5 ft, sterile / EO, 56.21.23P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V039000·2014-02-05
Nomad Recalls 2013 Dispatch Trailers Due to Door Lock Jamming Risk
Nomad is recalling 2013 Dispatch 14A, 20SS0, and 16AS0 trailers because a door lock defect could jam the deadbolt, trapping occupants inside.
Product
NOMAD — NOMAD DISPATCH 20SS0, DISPATCH 14A, DISPATCH 16AS0
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0896-2014·2014-02-05
Synergetics Recalls 23ga Mid-Field Endo Illuminator Due to Seal Failure
Synergetics Inc is recalling 26 units of 23ga Mid-Field Endo Illuminator devices because faulty seals on the outer pouch could fail, compromising sterility.
Product
23ga Mid-Field Endo Illuminator, Synergetics length 7.5 ft, sterile / EO, 56.22.23P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0856-2014·2014-02-05
Sorin S5/C5 Heart-Lung Machine Recalled for Pump Control Failures
Sorin Group is recalling S5/C5 Heart-lung machines and CP5 centrifugal pump systems due to pump speed control knob failures that result in no response.
Product
S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0857-2014·2014-02-05
Sorin CP5 Centrifugal Pump System Recalled for Control Knob Failures
Sorin Group is recalling 75 CP5 centrifugal pump systems due to reports of pump speed control knob failures that result in no response.
Product
CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0824-2014·2014-02-05
Siemens ACUSON SC2000 Ultrasound System Recalled for Loose User Interface
Siemens Medical Solutions is recalling 843 ACUSON SC2000 ultrasound systems because the user interface assembly may become loose and fall off.
Product
ACUSON SC2000 Ultrasound System; Power Input: 100-240VAC, 1600W Max, 50/60 Hz. Manufacturer: Siemens Medical Solutions USA, Inc. 685 East Middlefield Road Mountain View, CA 94043 SC2000 ultrasound imaging system is intended for Cardiac, neo-natal and fetal cardiac…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0858-2014·2014-02-05
Codman Certas Programmable Valves Recalled for Potential Malfunction
Codman & Shurtleff is recalling 1,460 Certas Programmable Valves used for hydrocephalus because they may not operate properly.
Product
Codman Certas Programmable Valve In Line Valve Only Product Code: 82-8800 Product Usage: The CODMAN CERTAS Programmable Valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for the management of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1431-2014·2014-02-05
Lambs Farm Lemon Butter Cookies Recalled for Undeclared Milk and Wheat Allergens
The Lambs Farm, Inc. is recalling Lemon Butter Cookies because the labels fail to declare milk and wheat allergens.
Product
Lemon Butter Cookies sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 10 oz.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0831-2014·2014-02-05
Philips Brilliance iCT Systems Recalled for Potential Image Artifacts
Philips Medical Systems is recalling Brilliance iCT and iCT SP systems because an artifact resembling a thrombus may appear on images.
Product
Brilliance iCT and Brilliance iCT SP These systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. May include signal analysis and display equipment, patient and equipment…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1048-2014·2014-02-05
Humco Recalls Mercuroclear Antiseptic Anesthetic Due to Microbial Contamination
Humco Holding Group is recalling Mercuroclear Antiseptic Anesthetic First Aid products due to contamination with Burkholderia sp. bacteria.
Product
Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and relieves pain and itching of minor cuts, scrapes, burns and insect bites. Aqueous solution. Active Ingredients Benzalkonium chloride 0.13% - First Aid antiseptic, Lidocaine hydrochloride 2.5% - External…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0882-2014·2014-02-05
Synergetics Recalls 72 Sterile Ophthalmic Laser Probes Due to Seal Failure
Synergetics is recalling 72 sterile ophthalmic laser probes because faulty seals on the outer pouch could fail, potentially compromising sterility.
Product
23ga Straight Fixed Extended Illuminated Laser Probe, Synergetics, length 7.5 ft, sterile / EO, 55.62.23P. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0891-2014·2014-02-05
Synergetics Recalls Two-Port Vitrectomy End Irrigators Due to Seal Failure
Synergetics is recalling specific lots of Two-Port Vitrectomy End Irrigators because faulty seals on the outer pouch could fail, compromising sterility.
Product
Two-Port Vitrectomy (TPV (tm)) Wide Field High Flow End Irrigator, Synergetics, inc., 19ga, length 7.0 ft, sterile / EO, 56.14. Packed 12 units per box. Manufactured for Synergetics, Inc., O'Fallon, MO.
Category
Medical Device
Distribution
Distributed nationwide