State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56651–56675 of 74005

HighFDA (Devices)·Z-0105-2015·2014-10-29
Philips Avalon Fetal Monitors Recalled for Software Measurement Error
Philips is recalling Avalon fetal monitors with specific software because automatic blood pressure measurements stop in certain modes.
Product
Philips Avalon Monitors with software revision J.30.58: Model Product FM20 M2702A ; FM30 M2703A ; FM50 M2705A Intended for: " Monitoring the physiological parameters of pregnant women " Non-invasive monitoring of fetal heart rates and movements.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0104-2015·2014-10-29
Philips IntelliVue Monitors Recalled for NBP Measurement Stoppage
Philips is recalling IntelliVue monitors with specific software revisions because the automatic blood pressure measurement series stops in time-synchronized mode.
Product
Philips IntelliVue Monitors with software revisions J.21.03, J.21.19. Model Product MP5 M8105A; MP5SC M8105AS; MP5T M8105AT; MP5 Upgrade M8105AU ; MP5SC Upgrade 866327 The monitors are intended to be used for monitoring and recording of, and to generate alarms…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0094-2015·2014-10-29
Zimmer Recalls 19 Hip Prosthesis Shells Due to Missing Threads
Zimmer, Inc. is recalling 19 Continuum Acetabular System hip prosthesis shells because they are missing polar boss threads.
Product
Continuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous 68mm, Prosthesis, Hip, Semi-Constrained, Metal/Polymer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0119-2015·2014-10-29
Aerogen Recalls FRIWO Power Adapters for Aeroneb Nebulizer Systems
Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.
Product
The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0057-2015·2014-10-29
Plum Organics Little Cremes Recalled for Choking Hazard
Plum, Inc. is recalling Little Cremes organic rice milk snacks because they are not softening as intended, posing a choking hazard to babies and young children.
Product
Plum Organics Little Cremes: Organic Rice Milk Snacks; Super Purples: Acai, Blackberry and Purple Carrot; Net Wt. 1 oz. (28 grams) 8 CT. USDA Organic; Dairy Free. Ingredients: ORGANIC SWEET POTATO PUREE, ORGANIC BLACKBERRY PUREE, ORGANIC APPLE PUREE, ORGANIC ACAI PUREE…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0044-2015·2014-10-29
Hospira Recalls Hydromorphone Hydrochloride Injection Due to Broken Vials
Hospira Inc. is recalling 145,600 vials of Hydromorphone Hydrochloride Injection because customer complaints confirmed that some glass vials may be broken or cracked, compromising sterility.
Product
HYDROMORPHONE HYDROCHLORIDE — HYDROMORPHONE HYDROCHLORIDE (HYDROMORPHONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0106-2015·2014-10-29
Ad-Tech Cueva Electrode Kits Recalled for Potential Wand Malfunction
Ad-Tech Medical Instrument Corporation is recalling Cueva Electrode Kits because the applicator wand may malfunction, potentially preventing monitoring of the VII cranial nerve.
Product
Box Label: 3 mm Cueva Electrode Kit, Sterile EO, Rx Only, REF. CNE1-3KDINX . Pouch labels: Each kit contains 3 pouches. 3 mm Cueva Electrode CNE-3X, Cueva Electrode Applicator Wand CNE-100X, Cueva Electrode Leadwire CNE-LW-2DINX. Box Label: 2 mm Cueva Electrode Kit, Sterile…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0121-2015·2014-10-29
Aerogen Nebulizer Power Adapter Recall Due to Broken Cover
Aerogen is recalling 323 FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover broke and dislodged from the adapter body.
Product
The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0061-2015·2014-10-29
Michael Foods Recalls Papetti's Pre-cooked Scrambled Eggs Due to Spoilage Risk
Michael Foods is recalling Papetti's Table Ready Refrigerated pre-cooked scrambled eggs because the product may be contaminated with a spoilage microorganism.
Product
Papetti's Table Ready Refrigerated pre-cooked scrambled eggs. Keep refrigerated 33 - 40 degrees F. Packaged in two different size configurations: (1) 12- 1.85 pound bags, Net Wt. 22.2 lbs (10.06 kg). Product code: 46025-85878. UPC Code: 1 07 46025 85878 9, and (2) 8…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0060-2015·2014-10-29
Michael Foods Recalls Papetti's Scrambled Eggs for Microbial Contamination
Michael Foods is recalling Papetti's Table Ready scrambled eggs due to potential contamination with a spoilage microorganism. The product was distributed nationwide.
Product
Papetti's Table Ready Refrigerated pre-cooked scrambled eggs with butter flavor. Keep refrigerated 33 - 40 degrees F. Packaged in 12- 1.85 pound bags with Net Wt. 22.2 lbs (10.06 kg). Product code: 46025-85877. UPC Code: 1 07 46025 85877 2.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0120-2015·2014-10-29
Aerogen Nebulizer Power Adapter Recall Due to Broken Cover
Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.
Product
The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0111-2015·2014-10-29
Signal Medical Recalls Total Knee Femoral Components Due to Packaging Compromise
Signal Medical Corporation is recalling 41 Symmetric Total Knee Femoral Components because their packaging was compromised. The components were distributed in Missouri and Panama.
Product
Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee Femoral Component is intended for use with Signal Medical Corp. Total Knee System for cemented use INA Total Knee Replacement. The femoral component is made of cobalt chromium alloy (ASTM F75).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0093-2015·2014-10-29
McKesson Cardiology Hemo Software Recall Due to Insufficient Maintenance Communication
McKesson Information Solutions LLC is recalling 625 McKesson Cardiology Hemo devices because communication regarding required annual maintenance testing was insufficient.
Product
McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0028-2015·2014-10-29
Bio-Pharm Recalls Acetaminophen Oral Suspension Due to Assay Failure
Bio-Pharm, Inc. is recalling one lot of Acetaminophen Oral Suspension Liquid 160mg/5mL because the product failed the assay at the 6-month timepoint.
Product
Rugby Children's Pain and Fever Acetaminophen Oral Suspension 160 mg/5 mL, Cherry Flavor, 2 FL. oz bottle, OTC, Distributed by: Rugby Laboratories Livonia, MI 48150, NDC 0536-3606-96 Major Children's Mapap Suspension Liquid, Cherry Flavor, 4 FL OZ bottle, OTC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0107-2015·2014-10-29
Mindray V-Series Patient Monitor Recalled for Drug Calculator Function Issue
Mindray DS USA is voluntarily recalling V-Series Patient Monitors due to a software issue with the Drug Calculator function.
Product
Mindray V21, Size: 515 mm X 335 mm X 685 mm, N.W.: 8 kg, G.W.: 11 kg, Qty:1 The V-Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for use include the monitoring of ECG waveform derived from…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0036-2015·2014-10-29
Forest Pharmaceuticals Recalls Bystolic Tablets for Dissolution Failure
Forest Pharmaceuticals is recalling Bystolic (nebivolol) 20 mg tablets because they failed a dissolution specification at a 6-month stability time point.
Product
Bystolic (nebivolol) tablets, 20 mg/tablet, packaged as 7 tablets/bottle/carton, and 12 bottles/trays, Professional Sample, Rx only, Forest Pharmaceuticals, Inc., St. Louis, MO. --- NDC 0456-1420-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0108-2015·2014-10-29
St. Jude Medical Recalls Fast-Cath Trio Hemostasis Introducer Due to Dilator Defect
St. Jude Medical is voluntarily recalling 220 units of the Fast-Cath Trio Hemostasis Introducer because the dilator is too small to allow guidewire advancement, potentially causing procedural delays.
Product
St Jude Medical, 10F Fast-Cath Trio" Hemostasis Introducer, REF # 406308, Sterile EO. The Fast-Cath Trio" Hemostasis Introducer consists of the following components: Port hemostasis adapter (3), Sheath (10F Cath-Lock"), dilator (10F) and 0.038 guidewire. See product…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0099-2015·2014-10-29
Intra Pump Infusion Systems Recalls CRN Crono Syringes Due to Needle Debris
Intra Pump Infusion Systems is recalling CRN Crono Syringes because the needle tips may contain clear debris. The recall affects 25,440 units distributed in the US and Canada.
Product
CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle"
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0118-2015·2014-10-29
Aerogen Recalls FRIWO Power Adapters for Aeroneb Nebulizer Systems
Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.
Product
The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0041-2015·2014-10-29
ZEE Aspirin Recalled for Incorrect Inactive Ingredient Labeling
ZEE Medical is recalling ZEE Aspirin 325mg tablets because the product label incorrectly lists inactive ingredients.
Product
ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0122-2015·2014-10-29
Siemens IMMULITE 1000 Cortisol Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling specific lots of IMMULITE 1000 Cortisol Assay reagents due to confirmed positive bias on controls.
Product
IMMULITE /IMMULITE 1000 Systems COR Cortisol, REF/Catalog Number LKC01, SMN 10381388, IVD. For in vitro diagnostic use with the IMMULITE 1000 Systems Analyzers for the quantitative measurement measurement of cortisol (hydrocortisone, Compound F) in serum, as an aid in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0101-2015·2014-10-29
Estill Medical Recalls Ultra Battery 1 for Insufficient Charging Capacity
Estill Medical Technologies is recalling 6,886 Ultra Battery 1 units because they may not reach full charge capacity within the standard 60-minute charging period.
Product
Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery 1 (TA-UB1) is a rechargeable power source for the Thermal Angel Blood and IV Fluid Infusion Warmer. The TA-UB1 battery was designed to provide sufficient power for the Thermal Angel to warm and deliver one…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0043-2015·2014-10-29
American Health Packaging Recalls Subpotent Methylprednisolone Tablets
American Health Packaging is recalling 2,005 cartons of Methylprednisolone 4 mg tablets because they failed to meet potency standards at a 6-month stability time point.
Product
METHYLPREDNISOLONE — METHYLPREDNISOLONE (METHYLPREDNISOLONE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·14V679000·2014-10-28
Spartan Recalls School Bus Chassis Due to Reversed ABS Connectors
Spartan is recalling 2011-2015 school bus chassis because reversed rear ABS connectors may cause wheels to lock up during braking.
Product
SPARTAN — SPARTAN SB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14E070000·2014-10-28
Meritor Wabco Recalls Quick Release Valves Due to Air Pressure Loss
Meritor Wabco is recalling specific Quick Release Valves where damaged rubber diaphragms may reduce air pressure, potentially compromising braking performance.
Product
SERVICE BRAKES, AIR recall
Category
Vehicle
Distribution
Distributed nationwide