State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28876–28900 of 73774

HighFDA (Devices)·Z-2019-2020·2020-05-27
K2M Aleutian Lordotic Spreader Recalled for Tip Breakage Risk
K2M, Inc. is recalling Aleutian Lordotic Spreader systems because the welded tips may break off during spinal procedures.
Product
K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90139, UDI # 10888857108523, Size 24x8mm, 18 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2043-2020·2020-05-27
Medline Silicone Foley Catheter Recalled Due to Loose Silicone Particulate
Medline Industries is recalling specific lots of silicone Foley catheters because loose silicone particulate was found on the device shaft.
Product
SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml - Product Usage: Medline Silicone Foley catheter is a flexible tubular device that is inserted through the urethra and used to drain urine into a collection device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2061-2020·2020-05-27
Bovie Medical Recalls Renuvion J-Plasma Precise Handpieces Due to Fracture Risk
Bovie Medical Corporation is recalling Renuvion/J-Plasma Precise Handpieces because unexpected stress fractures may cause the shaft to fragment during clinical use.
Product
Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B, BVX-270B, BVX-330B, BVX-270BPP, BVX- 330BPS, APYX-150B, APYX-270B, APYX-330B, APYX- 270BPP, and APYX-330BPS. Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2065-2020·2020-05-27
BD Posiflush SF Saline Flush Syringe Recalled for Packaging Holes
Becton Dickinson is recalling BD Posiflush SF Saline Flush Syringes because holes in the packaging may compromise the sterile field.
Product
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2040-2020·2020-05-27
Medline Recalls Surgical Kits Due to Potential Loss of Sterility
Medline is recalling 92,902 custom surgical convenience kits because packaging seal voids may have caused a loss of sterility on the outside of the foil pouch.
Product
Custom convenience kits containing Medline brand Sterile Pre-Saturated Povidone Iodine Sponge Products, labeled as follows: Part Description Part Number ABDOMINAL HYSTERECTOMY DYNJ906478 ABDOMINAL HYSTERECTOMY DYNJ906478A ACCESSORY HIP PACK-LF DYNJ0781865M ARTHRO/SHOULDER…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2050-2020·2020-05-27
Cardinal Health Recalls Urine Drug Controls Due to Temperature Abuse
Cardinal Health is recalling Alere Professional Urine Drug Controls (Lot KN00146) because they were stored outside approved temperature ranges, which may result in patient misdiagnosis.
Product
Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere Professional Cup Urine Drug Controls are compatible with all quantitative and qualitative drug detection procedures which are sufficiently sensitive to detect the control constituents.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2048-2020·2020-05-27
BD BBL Gram Stain Kit Recalled for Potential False-Positive Results
Becton Dickinson is recalling 1,469 BD BBL Gram Stain Kits because increased artifacts may be mistaken for bacteria, leading to false-positive results.
Product
BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For the differential staining of bacteria, Catalog Number: 212539 - Product Usage: Gram Stain Kits and Reagents are used to stain microorganisms from cultures or specimens by the differential Gram method.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2054-2020·2020-05-27
Skeletal Kinetics Recalls Cranio/Sculpt C Bone Void Filler Due to Sterilization Concerns
Skeletal Kinetics is recalling 125 units of Cranio/Sculpt C bone void filler because one unit may have been mispackaged and not sterilized.
Product
Cranio/Sculpt C, 10cc, Bone Void Filler, UDI: 00813845021129 - Product Usage: CRANIO/SCULPT C is a calcium phosphate bone void filler indicated for the repair or filling of neurosurgical burr holes, other cranial bone defects and craniotomy cuts with a surface area no larger…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2044-2020·2020-05-27
Medline Recalls Silicone Foley Catheters Due to Loose Particulate
Medline Industries is recalling specific lots of silicone Foley catheters because loose silicone particulate was found on the device shaft.
Product
SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml - Product Usage: Medline Silicone Foley catheter is a flexible tubular device that is inserted through the urethra and used to drain urine into a collection device.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20E033000·2020-05-27
Horizon Recalls Tekonsha Prodigy Electronic Brake Control Kits
Horizon Global is recalling certain Tekonsha Prodigy electronic brake control kits because they do not adequately warn drivers that foot pedal trailer braking is unavailable when hazard signals are active.
Product
ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2051-2020·2020-05-27
Cardinal Health Recalls Strep B Carrot Broth Due to Temperature Abuse
Cardinal Health is recalling Strep B Carrot Broth One-Step tubes because they were stored outside approved temperature ranges, which may lead to patient misdiagnosis.
Product
Strep B Carrot Broth One-Step, 16x100mm Tube, 6ml, Item code Z46BX - Product Usage: Intended to detect Group B Streptococcus (GBS) from anovaginal specimen collected from pregnant women. If pregnant woman is positive for GBS colonization, this will indicate a need for treatment…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V308000·2020-05-27
Thor Motor Coach Recalls 2020 Motorhomes Due to Manual Error
Thor Motor Coach is recalling 566 2020 motorhomes because the owner's manual incorrectly describes the automatic parking function, which could lead to vehicle rollaway.
Product
THOR MOTOR COACH — THOR MOTOR COACH, THOR SIESTA, SYNERGY, GEMINI, DELANO
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1282-2020·2020-05-27
West-Ward Recalls Ethacrynic Acid Tablets for Impurity Failures
West-Ward Columbus Inc is recalling Ethacrynic Acid Tablets USP, 25 mg, because the product failed impurity and degradation specifications.
Product
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·20127·2020-05-27
Primark Recalls Kitten Heel Court Shoes Due to Chromium Levels
Primark is recalling Wide Fit Kitten Heel Court Pumps because the leather insoles contain elevated levels of Chromium VI, posing a risk of skin irritation.
Product
Wide Fit Kitten Heel Court Pumps
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2064-2020·2020-05-27
Philips HeartStart MRx Processor Board Replacement Kits Recalled for Damaged Bags
Philips is recalling HeartStart MRx Processor Board PCA Replacement Kits because damaged ESD bags were used for storing components.
Product
HeartStart MRx Processor Board PCA Replacement Kits 453563478461, a component of the Philips HeartStart MRx Monitorl/Defibrillator - Product Usage: is intended for use in hospital and prehospital settings by qualified medical personnel trained in the operation of the device and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2045-2020·2020-05-27
Boston Scientific Recalls AMS 700 Reservoirs Due to Labeling Error
Boston Scientific is recalling five AMS 700 100 mL Spherical Reservoirs with InhibiZone because they were incorrectly labeled as a different model.
Product
AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the treatment of chronic, organic, male erectile dysfunction (impotence).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2067-2020·2020-05-27
DFINE Vertebral Hydraulic Assemblies Recalled for Incorrect Expiration Dates
Merit Medical Systems is recalling 228 DFINE Vertebral Hydraulic Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Hydraulic Assemblies: Hydraulic Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 1402 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological fractures…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2073-2020·2020-05-27
Capso Vision Recalls CapsoCam Plus Capsule Endoscopy Systems Due to Labeling Errors
Capso Vision, Inc. is recalling 44 CapsoCam Plus video capsule systems because incorrect serial number labels may lead to patient misdiagnosis.
Product
CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2020·2020-05-27
Merit Medical Recalls DFINE Vertebral Assemblies Due to Incorrect Expiration Dates
Merit Medical Systems is recalling 63 DFINE Vertebral Assemblies because the labels display a five-year expiration date instead of the correct two-year shelf life.
Product
DFINE Vertebral Assemblies: Hydraulic-Master Syringe Assembly, StabiliT Vertebral Augmentation System, Reference/Catalog number 3427 - Product Usage: is intended for percutaneous delivery of StabiliT ER2 Bone Cement in kyphoplasty procedures in the treatment of pathological…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1271-2020·2020-05-27
Mylan Recalls Aloprim Injection Vials Due to Discoloration
Mylan Institutional LLC is recalling 3,010 vials of Aloprim (allopurinol sodium) for Injection due to out-of-specification appearance and color results.
Product
ALOPRIM — ALOPRIM (ALLOPURINOL)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1272-2020·2020-05-27
InvaGen Recalls Gabapentin Tablets Due to Impurity Test Failure
InvaGen Pharmaceuticals is recalling 2,202 bottles of Gabapentin 600 mg tablets because they failed an impurity test during stability testing.
Product
GABAPENTIN — GABAPENTIN (GABAPENTIN)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2038-2020·2020-05-27
Pega Medical Recalls SLIM System Handle Due to Lot Number Mismatch
Pega Medical Inc. is recalling three units of the SLIM System handle because the lot number on the instrument does not match the packaging label.
Product
Orthopedic manual Surgical Instrument handle for Simple Locking Intra Medullary (SLIM) System - Product Usage: The SLIM handle is the grip for the SLIM driver in orthopedic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V301000·2020-05-26
Altec Recalls Aerial Devices With Incorrect Tow Hitch Load Ratings
Altec is recalling 2014-2020 Aerial Devices with Class 3 towing hitches that may have incorrect load ratings or damage from overloading, increasing crash risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V302000·2020-05-26
2020-2021 Keystone Cougar travel trailer cooktop fire hazard
Keystone is recalling 2020-2021 Cougar travel trailers because the cooktop may not be properly sealed from the furnace, causing burner flames to invert and increasing fire risk. Dealers will inspect and seal it free of charge.
Product
KEYSTONE — KEYSTONE COUGAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V300000·2020-05-23
AEV TraumaHawk Ambulances Recalled for Rear Brake Line Wear Risk
Halcore Group is recalling 2019-2020 AEV TraumaHawk ambulances because rear brake lines may wear from contact with suspension parts, risking brake loss.
Product
AEV — AEV TRAUMAHAWK
Category
Vehicle
Distribution
Distributed nationwide