State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

60726–60750 of 74011

HighFDA (Devices)·Z-0414-2014·2013-12-04
DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 4-7 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14037·2013-12-04
K2 Revo Kick Kickboards Recalled for Handle Detachment Hazard
K2 Sports is recalling K2 Revo Kick kickboards/scooters because the front assembly can break, causing the handle to detach and posing a fall hazard to riders.
Product
K2 Revo Kick kickboards/scooters
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0375-2014·2013-12-04
Plum Organics Baby Food Recalled for Post-Process Contamination
Plum Inc is recalling Kale, Apple & Greek Yogurt baby food pouches due to a manufacturing defect causing post-process contamination.
Product
Plum Organics Kale, Apple & Greek Yogurt Organics Baby Food- 3.5 oz. Pouch Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0350-2014·2013-12-04
MRM Recalls Gluten Free 60 vcaps Due to Chloramphenicol Contamination
Metabolic Response Modifier is recalling Gluten Free 60 vcaps because the product may contain trace amounts of the antibiotic chloramphenicol.
Product
Gluten Free 60 vcaps, sku#609492310194. 12 units per shipping carton/case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0388-2014·2013-12-04
Synthes Tensioning Device Recalled Due to Potential Mechanical Failure
Synthes USA HQ, Inc. is recalling 369 Tensioning Devices because the reaction fork may come loose, preventing the device from applying tension or releasing the wire.
Product
Synthes Tensioning Device The Synthes Osteogenesis System, MR Conditional is intended for fracture fixation (open and closed), pseudoarthrosis or non-unions of long bones, limb lengthening by epiphyseal or metaphyseal distraction, correction of bony or soft tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0418-2014·2013-12-04
DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2014·2013-12-04
DePuy Recalls Knee Instruments Due to Potential Tab Fracture
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs may fracture and remain in patients.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0377-2014·2013-12-04
Plum Inc Recalls Parsnip, Blueberry & Buckwheat Pouches for Contamination
Plum Inc is recalling Parsnip, Blueberry & Buckwheat pouches due to a manufacturing defect that led to post-process contamination.
Product
Parsnip, Blueberry & Buckwheat Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST COLLECTIVE, INC. EMERYVILLE, CA…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·13V608000·2013-12-04
Triumph Recalls 2013 Trophy SE Motorcycles Due to Center Stand Defect
Triumph is recalling 416 model year 2013 Trophy SE motorcycles because the left-hand center stand mount may fracture, potentially causing the bike to fall over while parked.
Product
TRIUMPH — TRIUMPH TROPHY SE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0405-2014·2013-12-04
Synthes Implant Holder Recalled Due to Breakage During Orthopedic Surgery
Synthes USA HQ, Inc. is recalling 548 Synfix (TM)-LR Implant Holders because they may break at the interface between the implant and the holder.
Product
Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder for Synfix (TM)-LR is a non-powered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0391-2014·2013-12-04
Synthes Matrix Coronal Bender Recall Due to Tip Breakage
Synthes USA is recalling 209 Matrix 5.5mm Coronal Benders because tips broke during use. The devices are used for spinal stabilization.
Product
Synthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: The Matrix 5.5.mm Left and Right Coronal Bender are used together to bend the 5.5 Matrix Rods in the coronal plane, and is intended for stabilization of the thoracic, lumbar, sacral, and/or iliac spine…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0412-2014·2013-12-04
DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2014·2013-12-04
Siemens Fluoroscopic X-Ray Systems Recalled for Radiation Malfunction
Siemens is recalling specific fluoroscopic x-ray systems due to a software defect that may cause radiation to continue longer than required, resulting in overexposed images.
Product
(Siemens Rad Fluoro Uro Systems) Ysio, Luminos Agile, Luminos dRF, and Uroskop Omnia systems with software version VC10 Image intensified fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0361-2014·2013-12-04
Plum Organics Baby Food Recalled for Post-Process Contamination Risk
Plum Inc is recalling specific lots of Plum Organics Raspberry, Spinach & Greek Yogurt Organic Baby Food due to a manufacturing defect that could lead to post-process contamination.
Product
Plum Organics Raspberry, Spinach & Greek Yogurt Organic Baby Food, 4 oz. pouch. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0420-2014·2013-12-04
DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 4-7 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0363-2014·2013-12-04
Plum Organics Baby Food Recalled for Manufacturing Defect
Plum Inc is recalling Spinach, Peas & Pear Organic Baby Food due to a manufacturing defect that led to post-process contamination.
Product
Plum Organics Spinach, Peas & Pear Organic Baby Food, 4 oz. pouch.. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0381-2014·2013-12-04
Biomet Recalls Oversized Security Blades for Carpal Tunnel Surgery
Biomet, Inc. is recalling 1,130 Security Blades for carpal tunnel surgery because they were manufactured oversized and may be difficult to advance through the mating clip.
Product
REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Use Only. Designed to release the transverse carpal ligament.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0396-2014·2013-12-04
Synthes Titanium Spinal Locking Caps Recalled for Post-Operative Loosening
Synthes USA is recalling 745 Titanium Minimally Invasive Reduction Screw System Locking Caps due to a risk of post-operative loosening if the construct is mis-aligned during final tightening.
Product
Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap, Part Number 04.631.502 Non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0408-2014·2013-12-04
Synthes Slipped Capital Femoral Epiphysis System Recalled for Drill Bit Breakage
Synthes USA is recalling 166 units of the Slipped Capital Femoral Epiphysis System because guide wires may stick and drill bits may break during surgery.
Product
Slipped Capital Femoral Epiphysis System Product Usage: Intended for fracture fixation of large bones and large bone fragments and for slipped capital femoral epiphysis, pediatric femoral neck fractures, intercondylar femur fractures and sacroiliac joint disruptions.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14038·2013-12-04
SRAM Recalls Bicycle Derailleurs Due to Fall Hazard
SRAM is recalling specific RED WiFLi rear derailleurs because a pivot pin can loosen, causing the derailleur to jam and posing a fall hazard.
Product
Bicycle chain derailleurs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0422-2014·2013-12-04
DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk
DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.
Product
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 2-3 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0357-2014·2013-12-04
Plum Organics Yogurt Mish Mash Recalled for Contamination
Plum Inc is recalling Plum Organics Tots Purple Roots and Fruits Yogurt Mish Mash due to a manufacturing defect that led to post-process contamination.
Product
Plum Organics Tots Purple Roots and Fruits Yogurt Mish Mash; 3.17 oz. Pouch; Also 12.69 oz. box. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0380-2014·2013-12-04
Plum Inc Recalls Kale, Apple & Greekstyle Yogurt Pouches
Plum Inc is recalling Kale, Apple & Greekstyle Yogurt pouches due to a manufacturing defect that led to post-process contamination.
Product
Kale, Apple & Greekstyle Yogurt Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST COLLECTIVE, INC. EMERYVILLE, CA 94608…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0401-2014·2013-12-04
Kraft and Polly-O String Cheese Recalled for Potential Spoilage
Kraft Foods Group is recalling specific varieties of Kraft and Polly-O String Cheese and String Cheese Twist products because they may spoil before their expiration dates, causing discoloration.
Product
Low-Moisture Part-Skim Mozzarella String Cheese, sold under Kraft brand or Polly-O brand and packaged with either 12, 16, 24, or 48 pieces of mozzarella cheese individually wrapped in plastic and sold in a plastic bag with a net weight respectively of 12 oz. (340g), 16 oz. (1…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0404-2014·2013-12-04
Kraft and Polly-O String Cheese Recalled for Potential Spoilage
Kraft Foods Group is recalling certain Kraft and Polly-O String Cheese products that may spoil before their expiration dates, causing discoloration.
Product
Low-Moisture Part-Skim Mozzarella String Cheese With Jalapeno Peppers, sold under Kraft brand or Polly-O brand and packaged with 12 pieces of mozzarella cheese with jalapeno peppers individually wrapped in plastic and sold in a plastic bag with a net weight of 10 oz. (283g).
Category
Food
Distribution
Distributed nationwide