State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55076–55100 of 74002

HighFDA (Devices)·Z-1281-2015·2015-03-25
Synthes Thumb Screws Recalled Due to Incorrect Stainless Steel Material
Synthes, Inc. is recalling 183 thumb screws for orthopedic aiming arms because incorrect raw material was used, which may lead to stress-corrosion cracking.
Product
Thumb Screw for the Synthes Recon Locking Aiming Arm for Lateral Entry Femoral Nails-EX (part number 03.010.048) and the Thumb Screw for the Aiming Arm for Titanium Cannulated Tibial Nails-EX (part number 03.010.052). The Recon Locking Aiming Arm for Lateral Entry Femoral…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1300-2015·2015-03-25
CooperSurgical Recalls MediChoice Infant Heel Warmers for Burn Risk
CooperSurgical is recalling MediChoice Infant Heel Warmers because products without expiration dates have a remote potential for minor burns.
Product
MediChoice WarmGel Infant Heel Warmer, Item # 1643069911 MediChoice Liquid Infant Heel Warmer, Item # 1643069912 Single Use and Disposable. Distributed by: Owens & Minor. To provide gentle heat to increase blood flow and enhance infant blood sample collection
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1450-2015·2015-03-25
Goya Recalls Kirby Black Beans and Goya Black Bean Soup for Peanut Contamination
Goya Foods is recalling Kirby Black Beans Creole Seasoning and Goya Black Bean Soup due to possible peanut contamination.
Product
Kirby Black Beans Creole Seasoning Net Wt. 29 oz. Packed for Kirby Foods Inc., Miami, Florida 33172 Product of Dominican Republic UPC 0 7738512346 4
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1273-2015·2015-03-25
Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes because some packages may have open seals, potentially compromising sterility.
Product
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: SafeStep Port Access Kit 22G x 0.75in , SafeStep Port Access Kit 22G x 0.75in with Y-Site, SafeStep Port Access Kit 22G x 1 in , SafeStep Port Access Kit 20G x 0.75in , SafeStep Port Access Kit…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1280-2015·2015-03-25
Mindray Recalls Passport V Monitors Due to Inaccurate Blood Pressure Readings
Mindray is recalling 519 Passport V Monitors because the invasive blood pressure function may provide incorrect measurements.
Product
Passport V Monitor, Multiparameter Patient Monitor(with Arrhythmia Detection and Alarms) Intended for intra hospital use under the direct supervision of a licensed healthcare practitioner.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1272-2015·2015-03-25
Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals
Bard Access Systems is recalling 16,410 units of BD PosiFlush Saline Flush Syringes included in various device kits because open seals may impact product sterility.
Product
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerLoc Port Access Kit 19G x 1 in, PowerLoc Port Access Kit 20G x 1 in, , , PowerLoc Port Access Kit 20G x 1.5in, PowerLoc Port Access Kit 20G x 0.75in, , , PowerLoc Port Access Kit 22G x 1 in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2015·2015-03-25
Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain catheter kits because open seals may compromise product sterility.
Product
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerGlide Midline Catheter Full Kit (20G) (8cm), PowerGlide Midline Catheter Maximal Barrier Tray (20G) (8cm), PowerGlide Midline Catheter Full Kit (20G) (10cm), The syringe is used to pre-flush…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1271-2015·2015-03-25
Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in various catheter kits because open seals may compromise product sterility.
Product
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Bard Poly Midline 3F Full Tray (Single-Lumen) (with Microintroducer), Bard Poly Midline 3F Maximal Barrier Tray (Single-Lumen), Bard Poly Midline 4F Maximal Barrier Tray (Single-Lumen) (with…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15E024000·2015-03-25
Gillig Recalls One Recaro Bus Driver Seat Due to Seat Belt Defect
Gillig is recalling one Recaro bus driver seat because a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in a crash.
Product
SEAT BELTS recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1270-2015·2015-03-25
GE Healthcare Ventilators Recalled for Caster Mounting Hardware Failure Risk
GE Healthcare is recalling specific ventilator models due to a potential failure of the caster mounting hardware that could cause the device to fall or tip over.
Product
GE Healthcare Engstrom Carestation, Engstrom Pro, Cart Only S/5 EC. GE model numbers 1505-8538-000, 1505-9000-000, and 1505-9003-000. Ventilators.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1269-2015·2015-03-25
Baxter MiniCap with Povidone-Iodine Solution Recalled for Sponge Defects
Baxter Healthcare is recalling MiniCap with Povidone-Iodine Solution units for hemodialysis because the product may have separating or protruding sponges.
Product
MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1279-2015·2015-03-25
GE Healthcare Recalls Nuclear Medicine Systems Due to Collimator Detachment Risk
GE Healthcare is recalling 472 nuclear medicine systems worldwide because a collimator may fall off during rotation. No injuries have been reported.
Product
GE Healthcare Millennium VG, Discovery VH and VariCam Nuclear Medicine systems, all configurations. Product Usage: The intended use of the system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1295-2015·2015-03-25
Transonic Hemodialysis Monitor Recall Due to Inaccurate Flow Measurements
Transonic Systems Inc is recalling Hemodialysis Monitors that may display zero or low flow values, preventing accurate measurements during dialysis.
Product
Transonic Hemodialysis Monitor, Model HD03 -- Product Usage: The Hemodialysis Monitor is intended for use by trained medical personnel to measure delivered blood flow, vascular access recirculation, vascular access blood flow and cardiac output on patients receiving…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1299-2015·2015-03-25
Fisher Brand Infant Heel Warmers Recalled for Burn Risk
CooperSurgical is recalling Fisher Brand Gel and Liquid Infant Heel Warmers because products without expiration dates pose a remote potential for minor burns.
Product
Fisher Brand Gel Infant Heel Gel Warmers, Cat. No.: 22-024647 Fisher Brand Liquid Infant Heel Warmer, Cat. No: 22-024646 To provide gentle heat to increase blood flow and enhance infant blood sample collection
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1451-2015·2015-03-25
Goya Black Bean Soup Recalled for Possible Peanut Contamination
Goya Foods is recalling 29-ounce cans of Black Bean Soup and Kirby brand black beans due to possible peanut contamination.
Product
Goya Black Bean Soup Net Wt. 29 oz. Goya Foods, Secaucus, NJ 07096 Product of Dominican Republic UPC 0 4133102081 7
Category
Food
Distribution
Distributed nationwide
HighNHTSA·15V175000·2015-03-25
Ford Recalls 2011-2015 F-Series Trucks With Emergency Vehicle Packages
Ford is recalling 6,322 model year 2011-2015 F-350, F-450, and F-550 trucks equipped with ambulance or fire engine packages due to a software defect that may cause the engine to shut down unexpectedly.
Product
FORD — FORD F-550 SD, F-450 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1292-2015·2015-03-25
Baxter HomeChoice Pro APD System Recalled for Occluder Defect
Baxter Healthcare is recalling 75 HomeChoice Pro APD systems because the occluder may have sharp edges or separate, causing system errors or therapy termination.
Product
The HomeChoice Pro APD System is a peritoneal dialysis system. The HomeChoice Pro Automated Personal Cycler peritoneal dialysis system is intended for automatic control of dialysate solution exchange in the treatment of pediatric and adult renal failure patients undergoing…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1286-2015·2015-03-25
Smiths Medical Recalls CADD Medication Cassette Reservoirs Due to Leak Risk
Smiths Medical is recalling specific lots of 50mL CADD Medication Cassette Reservoirs because they may leak at the sealing area. No serious injuries or deaths have been reported.
Product
CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1297-2015·2015-03-25
Siemens E.CAM Systems Recalled for Incorrectly Assembled Radial Motor Drives
Siemens Medical Solutions is recalling E.CAM emission computed tomography systems because radial motor drives replaced during service were assembled backwards.
Product
E.CAM emission computed tomography system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1301-2015·2015-03-25
CooperSurgical Recalls NovaPlus Infant Heel Warmers Due to Burn Risk
CooperSurgical is recalling NovaPlus infant heel warmers because products without expiration dates may cause minor burns.
Product
NovaPlus Brand Warm Gel Infant Heel Gel Warmer, Item # V6391 NovaPlus Brand Liquid Heal Warmer. Item #V6393 Single Use and Disposable To provide gentle heat to increase blood flow and enhance infant blood sample collection
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0413-2015·2015-03-25
Mylan Recalls Subpotent Nicardipine Hydrochloride Injection Vials
Mylan Institutional LLC is recalling specific lots of Nicardipine Hydrochloride Injection because the product failed potency and impurity specifications.
Product
Nicardipine Hydrochloride Injection, 25 mg/10 ml (2.5 mg/mL),10 mL single dose vial, Rx only, Manufactured in India for: Mylan Institutional LLC, Rockford, IL 61103, NDC 67457-224-10
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0419-2015·2015-03-25
Tarmac Recalls Antacid Liquid Due to Microbial Contamination
Tarmac Products is recalling specific lots of Antacid Liquid Regular Strength because they failed microbiological testing at the 12-month time point.
Product
Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200 mg, Magnesium hydroxide 200 mg, Simethicone 20 mg (in each 5 mL, 1 teaspoon), Mint flavor, 12 fl oz (355 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0073-02…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1275-2015·2015-03-25
Bard Access Systems Recalls BD PosiFlush Saline Flush Syringes Due to Open Seals
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain device kits because open seals may compromise product sterility.
Product
BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Groshong Midline Bard MYPICC Kit 4F (Single-Lumen) The syringe is used to pre-flush the catheter prior to placement and may also be used to verify patency post-placement.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1296-2015·2015-03-25
Siemens Symbia E SPECT Systems Recalled for Incorrect Radial Motor Assembly
Siemens Medical Solutions is recalling 419 Symbia E SPECT systems worldwide because radial motor drives were incorrectly assembled backwards during a customer service action.
Product
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1284-2015·2015-03-25
St Jude Medical Recalls TactiSys Quartz Pack for Configuration Update
St Jude Medical is recalling 89 TactiSys Quartz Packs because a configuration update is needed to ensure the device appropriately recognizes all TactiCath catheters.
Product
TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias that allows visualization of the contact force between TactiCath quartz catheter tip and the heart wall. Product Usage: This device is indicated for…
Category
Medical Device
Distribution
Distributed nationwide