State

US Virgin Islands product recalls

73,187 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: 30
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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13726–13750 of 73364

HighFDA (Devices)·Z-0221-2024·2023-11-15
Pendant Patient Alarm Battery Defect Prevents Emergency Alerts
Securitas Healthcare LLC recalls Arial Water Resistant Pendants (Models 59361 and 2560-59361) because premature battery depletion may prevent emergency alarms from reaching the wireless alert system. Affected patients may not receive emergency assistance when needed.
Product
Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0255-2024·2023-11-15
Stryker Disposable Bipolar Forceps Recall for Incorrect Expiration Date Labeling
Stryker Corporation recalls Disposable Spetzler-Malis Bipolar forceps due to labeling error. Products are labeled for 54-month shelf life but have actual 36-month shelf life, risking use of expired sterile surgical equipment.
Product
Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 0.5MM, Catalog Number 6780-230-005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0240-2024·2023-11-15
Stryker Surgical Forceps Recalled for Incorrect Expiration Date Label
Stryker Corporation is recalling 2,321 units of disposable surgical forceps due to a labeling error. The label indicates a 54-month shelf life, but the products actually expire in 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 18CM SM DISP BAYONET 1.5MM TIP, Catalog Number 6760-180-015
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0243-2024·2023-11-15
Stryker disposable surgical forceps recalled for incorrect expiration date labeling
Stryker Corporation is recalling 2,321 Spetzler-Malis bipolar surgical forceps due to incorrect expiration date labeling. The product label states a 54-month shelf life when the actual shelf life is only 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 23CM SM DISP BAYONET 1.0MM TIP, Catalog Number 6760-230-010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0239-2024·2023-11-15
Disposable Spetzler-Malis Bipolar Forceps Recalled for Incorrect Shelf Life Label
Stryker is recalling 2,321 disposable Spetzler-Malis Bipolar forceps due to a labeling error showing an incorrect shelf life. The product label indicates 54 months, but the actual shelf life is 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 18CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-180-005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0274-2024·2023-11-15
DigitalDiagnost 4 Radiographic Systems Risk of Ceiling Mount Failure
DigitalDiagnost 4 High Performance radiographic systems may fail and fall from ceiling mounts. The FDA recalls 366 units distributed nationwide.
Product
DigitalDiagnost 4 High Performance, used to acquire, process, store, display and export digital radiographic images.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0241-2024·2023-11-15
Stryker Disposable Spetzler-Malis Bipolar Forceps Expiration Date Mislabeled
Stryker Corporation recalled disposable surgical forceps with mislabeled expiration dates. The product label incorrectly indicates a 54-month shelf life when the actual shelf life is 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 20CM SM DISP BAYONET 0.5MM TIP, Catalog Number 6760-200-005
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2024·2023-11-15
Stryker Bipolar Surgical Forceps Recalled for Incorrect Expiration Label
Stryker Corporation is recalling 2,321 units of disposable bipolar surgical forceps with incorrect expiration dates on their labels. The devices are labeled with a 54-month shelf life when the actual shelf life is 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 1.0MM TIP, Catalog Number 6770-180-010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0229-2024·2023-11-15
Azurion medical imaging systems recalled for missing safety spacer and warning label
Philips Azurion IGTS Fixed Systems delivered to U.S. territories lack required safety components. The Source-to-Skin Distance Spacer and warning label are missing from affected units.
Product
Azurion IGTS Fixed Systems
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0133-2024·2023-11-15
Medical administration set for radiation therapy recalled due to leakage risk
B. Braun Medical recalls THERASPHERE ADMIN SET due to manufacturing defects causing potential leakage. Leakage may delay therapy, increase bloodstream infection risk, and expose patients and healthcare workers to hazardous medication.
Product
THERASPHERE ADMIN SET, Article No. 7M2650. Canada only. Sterile, single use administration set used to deliver Yttrium-90 glass microspheres for internal radiation therapy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0095-2024·2023-11-15
FDA Recalls Deferasirox Tablets for Failed Dissolution Specifications
Glenmark Pharmaceuticals is recalling Deferasirox 500mg tablets nationwide due to failed dissolution specifications affecting approximately 5,856 bottles across multiple lots.
Product
DEFERASIROX — DEFERASIROX (DEFERASIROX)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0227-2024·2023-11-15
Medical imaging systems recalled for missing safety spacer and warning label
Philips is recalling Integris-Allura IGTS Fixed Systems delivered to Puerto Rico, Guam, and the Virgin Islands due to missing Source-to-Skin Distance Spacers and required warning labels.
Product
Integris-Allura IGTS Fixed Systems
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0288-2024·2023-11-15
EVIS EXERA III Gastrointestinal Videoscope Recalled Due to Sterilization Failures
Olympus Corporation is recalling 1,687 units of the EVIS EXERA III Gastrointestinal Videoscope nationwide due to sterilization failures that may occur when devices are reprocessed without adequate drying time in the endoscope channel.
Product
EVIS EXERA III Gastrointestinal Videoscope
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0090-2024·2023-11-15
Prescription Drug Recalled Due to Failed Dissolution Specifications
Amneal Pharmaceuticals is recalling Extended Phenytoin Sodium capsules nationwide (lot HM03221A) due to failed dissolution specifications, which means the tablets may not dissolve as intended.
Product
EXTENDED PHENYTOIN SODIUM — EXTENDED PHENYTOIN SODIUM (PHENYTOIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0230-2024·2023-11-15
Surgical C-arm Systems Recalled for Missing Warning Labels and Tube-Spacers
Philips recalled surgical C-arm systems in US territories without required warning labels and missing the Source-to-Skin Distance Spacer. Facilities should contact Philips for instructions on obtaining missing components.
Product
Veradius Unity Mobile Surgery C-arm
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0226-2024·2023-11-15
Surgical C-arm systems recalled for missing warning label and spacer
Philips is recalling Zenition 50 & 70 surgical C-arm systems distributed to Puerto Rico, Guam, and the Virgin Islands due to missing warning labels and safety spacers. These missing components may compromise radiation safety during surgical use.
Product
Zenition 50 & 70 Mobile Surgery C-arm
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0228-2024·2023-11-15
X-ray imaging systems recalled for missing warning label and spacer
Philips X-ray imaging systems delivered to Puerto Rico are missing warning labels and Source-to-Skin Distance Spacers. These missing safety components could affect user safety during imaging procedures.
Product
Allura Xper IGTS Fixed Systems
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0272-2024·2023-11-15
DigitalDiagnost 4 Ceiling-Mounted X-Ray Units Recall for Fall Hazard
Philips is recalling 13 DigitalDiagnost 4 Chest/Emergency radiographic imaging units due to a potential for ceiling-mounted units to fail and fall, posing injury risk.
Product
DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0129-2024·2023-11-15
SA3000 intravenous adapters recalled for manufacturing defect causing leakage
B. Braun is recalling SA3000 intravenous adapters due to a manufacturing defect that may cause leakage. This could delay therapy, increase bloodstream infection risk, and expose patients and workers to hazardous medication.
Product
SA3000 VENTED MICRO SPIKE ADAPTER, REF No. 418121, for intravenous use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0132-2024·2023-11-15
IV Injection Set Recall: Risk of Leakage and Bloodstream Infection
B. Braun Medical is recalling 12,800 units of TERUMO IV injection sets (Lot 0061753485) due to a manufacturing defect that may cause leakage, delaying therapy and increasing risk of bloodstream infection.
Product
TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV, Article No. 7S3070. Singapore only. IV injection set.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0290-2024·2023-11-15
Medical device blood oxygenation system recalled due to defective weld
Maquet Medical Systems USA is recalling 1,022 Cardiohelp-i blood oxygenation systems due to an insufficient weld on a critical component that may break under manual force.
Product
Cardiohelp-i, blood oxygenation and carbon dioxide removal system, Part Numbers 701072780 (Cardiohelp-i), 701068550 (Slide Rail Holder)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0250-2024·2023-11-15
Disposable Bipolar Forceps Recalled for Incorrect Expiration Date Labeling
Stryker Corporation is recalling 2,321 units of Disposable Spetzler-Malis Bipolar forceps due to incorrect expiration date labeling. The product label indicates a 54-month shelf life, but the actual shelf life is 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 23CM IM DISP BAYONET 0.5MM TIP, Catalog Number 6770-230-005
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0257-2024·2023-11-15
Stryker Bipolar Forceps Recalled for Incorrect Expiration Date Label
Stryker Corporation is recalling 2,321 units of Disposable Spetzler-Malis Bipolar forceps due to incorrect expiration date labeling. The label states a 54-month shelf life when the actual shelf life is 36 months.
Product
Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 1.5MM, Catalog Number 6780-230-015
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0094-2024·2023-11-15
Oxycodone Tablets Recalled for Lower Potency Than Labeled
OXAYDO oxycodone 7.5 mg tablets distributed nationwide are being recalled because they contain lower potency than labeled. The affected lot is 22W02 with expiration 01/31/2025.
Product
OXAYDO — OXAYDO (OXYCODONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0087-2024·2023-11-15
Buprenorphine HCl Injection Recalled for Crystallization Defect
Buprenorphine HCl injection is being recalled nationwide due to white crystalline agglomeration found in stored product samples during routine inspection.
Product
BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide