State

US Virgin Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28226–28250 of 73762

SevereFDA (Devices)·Z-2613-2020·2020-07-22
Skeletal Kinetics Recalls Osteovation EX Bone Void Filler Kits
Skeletal Kinetics is recalling Osteovation EX bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.
Product
OSTEOVATION EX, 5CC, IMPACT FORMULA. Product Number: 390-0205, UDI: 813845020047 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2605-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt Flow Bone Void Filler Kits
Skeletal Kinetics is recalling 125 units of Craniosculpt Flow bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
CRANIOSCULPT, FLOW 5CC. Product Number: C-FLOW5CC, UDI: 813845020337 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2615-2020·2020-07-22
Skeletal Kinetics Recalls Osteovation RMX Bone Void Filler Kits
Skeletal Kinetics is recalling Osteovation RMX bone void filler kits because they may not maintain setting characteristics for the labeled shelf life, potentially increasing surgical time or causing bone formation issues.
Product
OSTEOVATION RMX 10CC. Product Number: 390-6002, UDI: 813845021099 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1386-2020·2020-07-22
Granules Pharmaceuticals Recalls Metformin Hydrochloride Extended-Release Tablets
Granules Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets due to FDA detection of N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
Product
METFORMIN — METFORMIN (METFORMIN ER 500 MG)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2631-2020·2020-07-22
Skeletal Kinetics Recalls SKAFFOLD RENU FLOW Bone Void Filler Kits
Skeletal Kinetics is recalling SKAFFOLD RENU FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
SKAFFOLD RENU FLOW, 5CC. Product Number: SKMA-FL05, UDI: 813845020849 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2632-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt Flow Bone Void Filler Kits
Skeletal Kinetics is recalling Craniosculpt Flow bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
CRANIOSCULPT FLOW, CAN, 10CC, Product Number: C-FLOW10CC-CAN, UDI: 813845020375 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V422000·2020-07-22
Kia Recalls 2020 Stinger Vehicles for Steering Locking Defect
Kia is recalling 2020 Stinger vehicles with 2.0L Turbo-GDI engines because a steering component may be defective, potentially causing the steering to lock or become difficult while driving.
Product
KIA — KIA STINGER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2610-2020·2020-07-22
Medtronic Bone Void Filler Recalled for Potential Failure to Set
Skeletal Kinetics is recalling Medtronic Bone Void Filler kits because they may not maintain setting characteristics for the labeled shelf life, potentially increasing surgical time or causing bone formation issues.
Product
MEDTRONIC BONE VOID FILLER, LARGE. Product Number: C07B, UDI: 813845020511 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2635-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt Bone Void Filler Due to Setting Defects
Skeletal Kinetics is recalling 51 units of Craniosculpt bone void filler because the product may not maintain its setting characteristics for the labeled shelf life.
Product
CRANIOSCULPT, CMF IMPACT, 10CC, Product Number: C-CMF10CC, UDI: 813845020955 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2594-2020·2020-07-22
Skeletal Kinetics Recalls Acumed Callos Bone Void Filler Kits
Skeletal Kinetics is recalling Acumed Callos bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
ACUMED CALLOS INJECT 5CC. Product Number: 65-0005-S, UDI: 813845020238 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2624-2020·2020-07-22
Skeletal Kinetics Recalls SK Scaffold Impress 10CC Bone Void Filler Kits
Skeletal Kinetics is recalling SK Scaffold Impress 10CC bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.
Product
SK SKAFFOLD IMPRESS 10CC. Product Number: SKAF-IM10, UDI: 813845020795 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2604-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt Flow Bone Void Filler Kits
Skeletal Kinetics is recalling 35 units of Craniosculpt Flow bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
CRANIOSCULPT FLOW, OUS, 5CC Product Number: C-FLOW5CC-OUS, UDI: 813845020351 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2598-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt C Bone Void Filler Kits
Skeletal Kinetics is recalling 48 units of Craniosculpt C bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
CRANIOSCULPT C, 3CC. Product Number: C-C3CC, UDI: 813845021105 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20151·2020-07-22
Greenpan SimmerLite Dutch Ovens Recalled Due to Lid Explosion and Burn Hazards
The Cookware Company is recalling Greenpan SimmerLite Dutch Ovens because the lids can explode in the oven, posing burn and injury risks.
Product
Greenpan SimmerLite Dutch Ovens with Lid
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2621-2020·2020-07-22
Skeletal Kinetics Recalls Osteovationex Bone Void Filler Kits
Skeletal Kinetics is recalling Osteovationex 2cc Inject Formula bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
OSTEOVATIONEX 2CC INJECT FORMULA. Product Number: 390-0002, UDI: 813845020009 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2618-2020·2020-07-22
Skeletal Kinetics Recalls Osteovation Bone Void Filler Kits
Skeletal Kinetics is recalling Osteovation bone void filler kits because they may not maintain setting characteristics for the labeled shelf life, potentially increasing surgical time or causing bone formation issues.
Product
OSTEOVATION, 3CC, IMPACT FORMULA. Product Number: 390-2103, UDI: 813845020078 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2620-2020·2020-07-22
Skeletal Kinetics Recalls Osteovation Bone Void Filler Kits
Skeletal Kinetics is recalling Osteovation bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Product
OSTEOVATION, 5CC, INJECT FORMULA. Product Number: 390-2005, UDI: 813845020054 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2592-2020·2020-07-22
Skeletal Kinetics Recalls Acumed Callos Bone Void Filler Kits
Skeletal Kinetics is recalling Acumed Callos bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Product
ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2595-2020·2020-07-22
Skeletal Kinetics Recalls Acumed Impact Bone Void Filler Kits
Skeletal Kinetics is recalling 40 Acumed Impact bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
ACUMED IMPACT 10CC. Product Number: 65-0110-S, UDI: 813845020269 - Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2548-2020·2020-07-22
DiaSorin Simplexa VZV Direct Recalled for Potential False Negative Results
DiaSorin Molecular LLC is recalling Simplexa VZV Direct test kits due to a software malfunction that may cause false negative results for varicella-zoster virus.
Product
MOL3650 Simplexa VZV Direct - Product Usage: is intended for use on the LIAISON MDX instrument for the qualitative detection of varicella-zoster virus (VZV) DNA in cerebrospinal fluid (CSF) from patients with signs and symptoms of VZV infections of the central nervous system…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20155·2020-07-22
DownEast Recalls Folding Mattresses for Fire Hazard
DownEast Outfitters is recalling Mattress on the Go folding mattresses because they fail to meet federal flammability standards, posing a fire hazard.
Product
Mattress on the Go folding mattresses
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V423000·2020-07-22
Thor Motor Coach Motorhomes Recalled for Electrical System Fire Hazard
Thor Motor Coach is recalling certain 2019-2021 Freedom Elite and 2021 Four Winds motorhomes due to an incorrect converter breaker installation that can cause wiring to overheat and increase fire risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, FOUR WINDS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2612-2020·2020-07-22
Skeletal Kinetics Recalls Osteovation EX Bone Void Filler Kits
Skeletal Kinetics is recalling Osteovation EX bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Product
OSTEOVATION EX, 3CC, IMPACT FORMULA. Product Number: 390-0203, UDI: 813845020030 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2602-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt Flow Bone Void Filler Kits
Skeletal Kinetics is recalling Craniosculpt Flow bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.
Product
CRANIOSCULPT FLOW, CAN, 5CC. Product Number: C-FLOW5CC-CAN, UDI: 813845020344 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2599-2020·2020-07-22
Skeletal Kinetics Recalls Craniosculpt C Bone Void Filler Kits
Skeletal Kinetics is recalling Craniosculpt C bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.
Product
CRANIOSCULPT C, 5CC. Product Number: C-C5CC, UDI: 813845021112 - - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
Category
Medical Device
Distribution
Distributed nationwide