State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49276–49300 of 73995

HighFDA (Devices)·Z-1343-2016·2016-04-13
AngioDynamics Recalls NAMIC Convenience Kits Due to Needle Lumen Defect
AngioDynamics is recalling 136 NAMIC Convenience Kits because the needle inner lumen is too small to accept the intended 0.038-inch guidewire.
Product
NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK, REF Catalog No. 651919311, UPN Product No. H7496519193111 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1324-2016·2016-04-13
Fresenius Hemoflow F3 Dialyzer Recalled for Potential Header Leak
Fresenius Medical Care is recalling 1,650 Hemoflow F3 Dialyzers due to a potential header leak caused by improper torque.
Product
Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute and Chronic Hemodialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1317-2016·2016-04-13
Philips Recalls eValueMed Infant Heel Warmers and Transport Mattresses
Philips is recalling eValueMed infant heel warmers and transport mattresses because they lack expiration dates and warnings about overheating risks.
Product
eValueMed Infant Transport Mattress 301-1015, Distributed by Tri-anima A disposable heel warmer for use when circulation needs to be stimulated in the infant heel in order for blood sampling to occur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1344-2016·2016-04-13
AngioDynamics Recalls Renown Regional Medical Center Convenience Kits
AngioDynamics is recalling 100 Renown Regional Medical Center Convenience Kits because the needle inner lumen is too small to accept the intended guidewire.
Product
NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER, REF Catalog No. 65230029, UPN Product No. H965652300290, Product is packed as a box of 30 pieces, box label contains UPN Product No. H965652300291 Product Usage - This needle is intended to be placed over the guidewire to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1348-2016·2016-04-13
Ortho-Clinical VITROS 5600 Integrated System Recalled for Wiring Error
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because a wiring error may leave a module energized when the power cord is unplugged.
Product
VITROS 5600 Integrated System, Unique Device Identifier No. 10758750002740 & 10758750007110. Intended for use in the in vitro measurement of a variety of analytes of clinical interest.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1346-2016·2016-04-13
AngioDynamics Recalls NAMIC Convenience Kits Due to Needle Lumen Defect
AngioDynamics is recalling 45 NAMIC Convenience Kits because the needle inner lumen may be too small to accept a 0.038-inch guidewire.
Product
NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN Product No. H7496013198101 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1017-2016·2016-04-13
PerCoBa Whey Protein Isolate Recalled for Missing Milk Allergen Labeling
Immuno-Dynamics, Inc. is recalling PerCoBa Whey Protein Isolate with Colostrum because the labels fail to state that the product contains milk.
Product
PerCoBa Whey Protein Isolate with Colostrum, Dietary Supplement. Net Weight: 1 kg (2.2 lbs), Colostrum 3,000 mg. UPC 90576-00009. Immuno-Dynamics, Inc., 18000 Dodge Street, Fennimore, WI 53809.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1316-2016·2016-04-13
Recall of eValueMed Infant Heel Warmers and Transport Mattresses
Philips is recalling eValueMed Infant Heel Warmers and Transport Mattresses because they lack expiration dates and warnings about overheating risks after shelf life.
Product
evaluemed Infant Heel Warmer 301-1223; Distributed by Tri-anim A disposable heel warmer for use when circulation needs to be stimulated in the infant heel in order for blood sampling to occur
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16142·2016-04-13
Rollerblade USA Recalls Inline Skating Helmets Due to Head Injury Hazard
Rollerblade USA is recalling about 500 Maxxum inline skating helmets because the plastic shell can crack, causing the helmet to shift and potentially result in head injuries.
Product
Rollerblade inline skating helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1016-2016·2016-04-13
Immuno-Dynamics Recalls PerCoBa Colostrum Supplement for Missing Milk Labeling
Immuno-Dynamics is recalling PerCoBa and Synertek colostrum supplements because the labels fail to state that the products contain milk.
Product
PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 6.4%. Net Contents: 4 oz. Immuno-Dynamics, Inc. , PO Box 544 Perry, Iowa 50220
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16E034000·2016-04-13
Nitrous Outlet Recalls Nitrous Solenoid Valves Due to Welding Defect
Nitrous Outlet is recalling specific .122 Nitrous Solenoid valves due to improper welding that may cause the piston to eject under pressure, posing an injury risk.
Product
FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1326-2016·2016-04-13
Synthes Recalls Titanium Low Profile Neuro Screws Due to Thread Defect
Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, which may affect the device's structural integrity.
Product
Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V212000·2016-04-13
Strick Recalls 2004 Single Axle Van Trailers for Rear Impact Guard Defect
Strick Trailers is recalling 460 model year 2004 single axle van trailers because rear impact guard gussets may increase injury risk in crashes.
Product
STRICK — STRICK SINGLE AXLE VAN TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1347-2016·2016-04-13
GE Medical Systems Recalls SIGNA Pioneer MR Systems Due to Ferrous Material Risk
GE Medical Systems is recalling 16 SIGNA Pioneer MR systems because ferrous material in the Table Control Box could cause unexpected attraction to the magnetic field during servicing, posing a risk of serious injury to personnel.
Product
SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1273-2016·2016-04-13
Focus Diagnostics Recalls Simplexa Direct Amplification Discs for Diagnostic Errors
Focus Diagnostics is recalling Simplexa Direct Amplification Discs because they may cause false test results or error codes.
Product
Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2650, MOL1451, MOL1452, MOL1455
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1328-2016·2016-04-13
MicroAire PAL-R4011XL Cannula Recalled Due to Breakage During Surgery
MicroAire is recalling PAL-R4011XL cannulas because three reports indicated the devices bent or broke during surgical procedures.
Product
MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1345-2016·2016-04-13
AngioDynamics Recalls NAMIC Convenience Kits Due to Needle Lumen Defect
AngioDynamics is recalling 8 NAMIC Convenience Kits because the needle inner lumen is too small to accept the intended guidewire.
Product
NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT, REF Catalog No. 60080094, UPN Product No. H749600800941 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1331-2016·2016-04-13
Applied Medical Resources Recalls Epix Universal Clip Applier Kits
Applied Medical Resources is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.
Product
STD KIT GK213, AME Standard Kit 15 Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1320-2016·2016-04-13
Cardinal Health Recalls Gomco Style Circumcision Clamp Trays Due to Labeling Error
Cardinal Health is recalling Gomco Style Circumcision Clamp Trays because two lots were labeled as containing 1.1cm clamps but actually contained 1.3cm clamps.
Product
Gomco Style Circumcision Clamp Trays is an instrument used to compress the foreskin of the penis during circumcision of a male infant.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1349-2016·2016-04-13
Siemens PACS Software Recall for Incorrect Distance Measurements
Siemens Medical Solutions is recalling 49 PACS systems because they may display incorrect distance measurements when used with certain modalities and syngo Imaging.
Product
A Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images, including digital mammography images.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1014-2016·2016-04-13
PerCoBa Colostrum Capsules Recalled for Incorrect Milk Allergen Labeling
Immuno-Dynamics, Inc. is recalling PerCoBa Colostrum Capsules because the labels failed to state 'contains milk.' The product was distributed nationwide and internationally.
Product
PerCoBa Colostrum Capsules, Dietary Supplement, Colostrum (bovine) 1g. 120 capsules. UPC 90576-00011. Allergen statement: contains dairy. Distributed by: Immuno-Dynamics, Inc., 1800 Dodge Street, Fennimore, WI 53809.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0806-2016·2016-04-13
Meditech Formula 3 Injection Recalled Due to Expired Active Ingredient
Meditech Laboratories is recalling Formula 3 Injection vials because the active ingredient expired before the labeled Beyond Use Date.
Product
Formula 3 (Papaverine 20 mg, Phentolamine 3 mg, Atropine 0.2 mg, PGE 20 mcg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1015-2016·2016-04-13
Immuno-Dynamics Recalls Colostrum Lozenges for Allergen Labeling Error
Immuno-Dynamics, Inc. is recalling PerCoBa and Synertek colostrum lozenges because the labels state 'contains dairy' instead of 'contains milk.'
Product
Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the following sizes and Brand names: 1. PerCoBa, UPC 90576-00006. 100 Lozenges Distributed by: Immuno-Dynamics, Inc., Fennimore, WI 53809; 2.…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1332-2016·2016-04-13
Applied Medical Recalls Epix Universal Clip Appliers Due to Loading Defect
Applied Medical Resources Corp is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.
Product
STD KIT GK260, Standard Set 360 Z Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1329-2016·2016-04-13
Applied Medical Recalls Epix Universal Clip Appliers Due to Loading Mechanism Defect
Applied Medical Resources Corp is recalling CA500 Epix Universal Clip Appliers due to a potential loading mechanism nonconformance. The recall affects 1,771 units distributed in the U.S. and internationally.
Product
CA500 Epix Universal Clip Applier Product Usage: The Epix disposable laparoscopic clip applier is indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide