State

US Virgin Islands product recalls

73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18001–18025 of 73396

HighFDA (Devices)·Z-0378-2023·2022-12-14
Bipolar Forceps Recalled for Missing Power Supply and Cleaning Instructions
Carefusion 2200 Inc is recalling 203 units of V. Mueller SEMKIN Bipolar Forceps due to incomplete Instructions for Use. The IFU is missing critical content related to power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller" SEMKIN BIPOLAR FORCEPS WITH STOP, 0.7MM TIP OVERALL LENGTH 5-1/2" (140MM), REF F-1040
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2023·2022-12-14
LineSider Spinal System Screws Recalled for Potential Weld Separation
Integrity Implants is recalling 1,702 LineSider Spinal System pedicle screws due to potential weld separation between screw head components that could result in device failure.
Product
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
Carefusion is recalling 418 units of bipolar surgical forceps because the provided instructions lack critical content about power supply interface and maintenance. Complete manufacturer instructions are necessary for safe device operation.
Product
CareFusion V. Mueller SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM) , REF F-1002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0401-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Use and Maintenance Instructions
CareFusion bipolar forceps recalled due to incomplete Instructions for Use. Missing documentation covers power supply interface and cleaning/maintenance procedures.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5016
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0356-2023·2022-12-14
Dover Closed Urethral Tray Recalled for Potential Drainage Blockage Risk
Cardinal Health is recalling Dover Closed Urethral Catheter Trays due to potential blockage of the urinary drainage bag inlet port, which may prevent proper urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0358-2023·2022-12-14
Dover Urinary Catheter Drainage Tray Recall Due to Blockage Risk
Cardinal Health is recalling Dover Closed Urethral Tray urinary drainage systems due to potential blockage of the drainage bag inlet port, which may prevent proper bladder emptying and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 14 Fr/Ch (4.7 mm) Product Code: 3410 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0418-2023·2022-12-14
Spinal Implant Screws Recalled Due to Potential Weld Failure
LineSider Spinal System screws are recalled due to potential weld separation between components that could cause the Tulip Head to detach from the Screw Shank. The recall affects 1,227 screws distributed nationwide.
Product
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0413-2023·2022-12-14
Bipolar Forceps Recall: Incomplete Instructions for Surgical Device
BD recalls CareFusion bipolar forceps (Ref F-5301) due to incomplete Instructions For Use. The IFU is missing information about power supply interface and cleaning and maintenance.
Product
CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.5MM TIP, STRAIGHT, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0359-2023·2022-12-14
Dover Closed Urethral Tray Recalled Due to Drainage Port Blockage Risk
Cardinal Health recalls Dover Closed Urethral Tray due to potential blockage of the urinary drainage bag inlet port that could prevent urine drainage and increase risk of urinary retention if bladders are not emptied timely.
Product
Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0379-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Instructions for Use
Carefusion is recalling bipolar forceps due to missing instructions for use. The corrected instructions address power supply interface, cleaning, and maintenance.
Product
Carefusion V. Mueller SEMKIN BIPOLAR FORCEPS 1.5MM TIP, INSULATED OVERALL LENGTH 6" (150MM), REF F-1045
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0392-2023·2022-12-14
Carefusion Bipolar Forceps Recalled for Incomplete Instructions for Use
Carefusion is recalling the V. Mueller Jewelers Bipolar Forceps due to incomplete Instructions for Use missing power supply interface and cleaning/maintenance instructions. The recall affects 236 units distributed nationwide and internationally.
Product
Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP, STRAIGHT OVERALL LENGTH 4" (100MM), REF F-3000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0186-2023·2022-12-14
Betty Buzz Sparkling Grapefruit Recalled for Off-Odor
Betty Buzz LLC is recalling Betty Buzz Sparkling Grapefruit non-alcoholic beverage nationwide due to detected off-odor in the product. The recall affects 939 cases containing 22,536 bottles.
Product
Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container Description: 4 x 9oz Bottles in Pack 24 units per case
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0399-2023·2022-12-14
CareFusion Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion is recalling the V. Mueller Neuro/Spine Titanium Bipolar Forceps due to missing Instructions for Use content covering device power supply interface, cleaning, and maintenance procedures.
Product
CareFusion V. Mueller Neuro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 9-1/2" (240MM), REF F-5010
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0384-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Power Supply and Maintenance Instructions
Carefusion recalls bipolar forceps due to incomplete Instructions for Use missing power supply interface and maintenance guidance. No injuries reported.
Product
Carefusion V. Mueller CUSHING BAYONET BIPOLAR FORCEPS, 0.7MM TIP, INSULATED IRRIGATING OVERALL LENGTH 7-1/2" (190MM), REF F-1300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0412-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Missing Instruction Manual Content
CareFusion bipolar forceps recalled due to missing instructions on power supply interface and cleaning/maintenance procedures. Corrected documentation is now available.
Product
CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL LENGTH 6" (150MM) , REF F-5128
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0411-2023·2022-12-14
Bipolar Forceps Recall: Missing Power Supply and Cleaning Instructions
Carefusion is recalling bipolar forceps due to incomplete Instructions for Use. The IFU is missing content about power supply interface and cleaning procedures.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 0.5MM TIP, ANGLED-UP FINE OVERALL LENGTH 8-3/4" (225MM), REF F-5127
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0398-2023·2022-12-14
CareFusion Bipolar Surgical Forceps Recalled by FDA Class II Voluntary Action
CareFusion initiated a voluntary recall of bipolar forceps surgical instruments. The recall affects 4 units distributed nationwide and internationally.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0391-2023·2022-12-14
Surgical Bipolar Forceps Recalled for Incomplete Operating Instructions
Carefusion is recalling bipolar surgical forceps due to incomplete Instructions for Use. The missing instructions cover power supply interface and cleaning procedures.
Product
Carefusion V. Mueller" CUSHING BAYONET BIPOLAR FORCEPS, 2.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-2004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0396-2023·2022-12-14
CareFusion Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar forceps are recalled due to incomplete manufacturer instructions for use. Missing content covers power supply interface and device maintenance and cleaning procedures.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5002
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0417-2023·2022-12-14
CareFusion Bipolar Surgical Forceps Recalled for Incomplete Operating Instructions
CareFusion bipolar surgical forceps recalled for incomplete Instructions for Use. Documentation is missing information on power supply interface and cleaning procedures.
Product
CareFusion V. Mueller CUSHING MICRO BIPOLAR FORCEPS 0.7MM TIP, OVERALL LENGTH 6" (150MM), REF F-52000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0400-2023·2022-12-14
Bipolar forceps recalled for incomplete instructions for use
Carefusion V. Mueller bipolar forceps are recalled because their instructions are missing information on power supply interface and cleaning procedures. Users should obtain the complete manufacturer instructions.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 9-1/2" (240MM), REF F-5014
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0403-2023·2022-12-14
CareFusion Bipolar Forceps Recalled: Incomplete Instructions for Power Supply
CareFusion is recalling bipolar forceps units due to incomplete instructions for power supply interface and device maintenance. The recall affects devices distributed worldwide.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5022
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0381-2023·2022-12-14
Bipolar forceps recalled for incomplete instructions for use
Carefusion recalled certain bipolar forceps due to incomplete Instructions For Use. The IFU was missing content about the device's power supply interface and cleaning and maintenance procedures.
Product
Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, OVERALL LENGTH 7-1/2" (190MM), REF F-1111
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0389-2023·2022-12-14
Carefusion Bipolar Surgical Forceps Recalled for Missing Instructions
Carefusion 2200 Inc. is recalling 41 units of Hardy Bayonet Irrigating Bipolar Forceps due to incomplete instructions for use. The supplied instructions lack content about device power supply interface and maintenance procedures.
Product
Carefusion V. Mueller HARDY BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 0.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-1335
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0383-2023·2022-12-14
Bipolar Forceps Recall Due to Incomplete Instructions for Use
Carefusion is recalling 259 surgical bipolar forceps units because the Instructions for Use are missing critical information about power supply interface and maintenance procedures.
Product
Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-1113
Category
Medical Device
Distribution
Distributed nationwide