State

US Virgin Islands product recalls

73,190 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 30
Most recent: 2026-09-23

Of the 177 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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14951–14975 of 73367

SevereFDA (Food)·F-1271-2023·2023-07-26
Seasons Choice Mixed Fruit Recalled for Potential Listeria Contamination
Aldi's Seasons Choice Mixed Fruit is being recalled nationwide due to potential contamination with Listeria monocytogenes. Affected lot codes are FMX227603, FMX227604, and FMX227605.
Product
Seasons Choice Mixed Fruit, Strawberries, Pinneapple, Peaches & Mango, Net Wt 32 oz (2lb) 907g. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2150-2023·2023-07-26
Intra-Aortic Balloon Pump may fail to charge batteries, interrupting therapy
The Cardiosave Rescue Intra-Aortic Balloon Pump may lose battery charging ability in one or both bays, potentially interrupting therapy if disconnected from power. Low battery alarms may alert users before therapy stops.
Product
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2114-2023·2023-07-26
Abiomed Impella 5.5 pump recalled due to impeller blade damage risk
Abiomed is recalling the Impella 5.5 with SmartAssist pump due to a risk of impeller blade destruction when used with aortic valve replacement devices. Damage can result in low blood flow and systemic embolization, where broken pump pieces may enter the bloodstream.
Product
Impella 5.5 with SmartAssist intravascular micro axial blood pump, Product Numbers 0550-0008 and 1000100
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1269-2023·2023-07-26
Frozen Mixed Fruit Blend Recalled for Potential Listeria Contamination
SunOpta's Good & Gather brand frozen mixed fruit blend is recalled nationwide due to potential Listeria monocytogenes contamination. Affected consumers should not consume this product and should return it to the retailer.
Product
Good & Gather Mixed Fruit Blend Pineapple Chunks, Sliced Strawberries, Mango Chunks & Sliced Peaches. Net Wt 48 oz (3lb) 1.36kg. UPC 0 85239-04821 4. Keep Frozen. Dist. By Target Corp, Minneapolis, MN 55403
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1255-2023·2023-07-26
Frozen Pineapple Products Recalled Due to Listeria Contamination
Scenic Fruit Company recalls Cadia and Trader Joe's frozen pineapple products due to potential Listeria monocytogenes contamination. Consumers should not consume the recalled items.
Product
Cadia - Organic Pineapple Frozen Fruit, packaged in stand-up pouch, net wt. 10oz. Each case consists of 12 bags. Product of Mexico. UPC on Retail Bag: 815369014540 UPC on Case: 10815369014547 Cadia FS - Organic Frozen Pineapple Chunks, net wt. 5lbs. Each case consists of…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2111-2023·2023-07-26
Impella 2.5 blood pump recalled due to impeller blade damage risk
Impella 2.5 intravascular blood pumps may experience unintended interaction with aortic valve replacement stents, damaging impeller blades and reducing blood flow. Fragments may circulate through the bloodstream.
Product
Impella 2.5 intravascular micro axial blood pump, Product Number 005042
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2015-2023·2023-07-26
Olympus BRONCHOVIDEOSCOPE Model BF-Q170 Recalled Due to Combustion Risk
Olympus BRONCHOVIDEOSCOPE Model BF-Q170 is recalled nationally due to complaints of endobronchial combustion during therapeutic laser procedures, classified as FDA Class I.
Product
Olympus BRONCHOVIDEOSCOPE, Model Numbers BF-Q170
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1265-2023·2023-07-26
Frozen Triple Berry Blend Recalled for Potential Listeria Contamination
Good & Gather Triple Berry Blend, sold at Target, is being recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected product.
Product
Good & Gather Triple Berry Blend. Blueberries, Blackberries, & Red Raspberries. Net Wt 48 oz (3lb) 1.36kg, UPC 0 85239-04806 1. Keep Frozen. Dist By Target Corp. Minneapolis, MN 55403
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1254-2023·2023-07-26
Trader Joe's Organic Tropical Fruit Blend recalled for potential Listeria contamination
Trader Joe's Organic Tropical Fruit Blend is recalled due to potential contamination with Listeria monocytogenes from pineapple ingredients. The 16 oz. bags were distributed nationwide.
Product
Trader Joe s Organic Tropical Fruit Blend Pineapple, Banana, Strawberry, Mango, SKU #051191, packaged in pillow bags. Each case consists of 24 bags and each bag is 16 oz. UPC on retail bag: 00511919
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1256-2023·2023-07-26
Frozen Pineapple Chunks Recalled Due to Listeria Contamination Risk
SunOpta Grains and Foods Inc. is recalling nationwide frozen pineapple chunks sold under the 365 Whole Foods Market and Bulk Organic brands due to potential Listeria monocytogenes contamination.
Product
Pineapple Chunks packaged under the following brand names and sizes. 1. 365 Whole Foods Market, Net Wt 16 oz (1 lb) 454g UPC 0 99482-40854 1. Keep Frozen. Distributed by: Whole Foods Market, Austin, TX 78703. 2. 365 Whole Foods Market, Net Wt 10 oz (284g) UPC 0…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2115-2023·2023-07-26
Impella CP Blood Pump Recalled for Blade Destruction From Stent Interaction
Abiomed's Impella CP cardiac pump can be damaged by interaction with replacement heart valves, potentially causing blood clots. The FDA classified this as a Class I recall of 9,252 units worldwide.
Product
Impella CP intravascular micro axial blood pump, Product Number 0048-0032
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2011-2023·2023-07-26
Olympus OES Bronchofiberscope Models Recalled for Combustion Risk During Laser Procedures
Olympus is recalling OES Bronchofiberscope models due to reports of combustion during laser procedures. This poses a serious burn injury risk to patients.
Product
Olympus OES BRONCHOFIBERSCOPE BF Type, Model Numbers BF-XT40, BF-P60, BF-MP60, BF-1T60
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2014-2023·2023-07-26
Olympus EVIS EXERA Bronchoscope Recalled for Combustion Risk During Laser Procedures
The FDA recalls 284 Olympus EVIS EXERA bronchoscopes due to complaints of combustion during therapeutic laser procedures. Users should stop using affected models immediately.
Product
Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE, Model Number BF-XT160
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1262-2023·2023-07-26
Good & Gather Organic Frozen Cherries & Berries Recalled for Listeria Risk
SunOpta Grains and Foods is recalling Good & Gather Organic frozen cherries and berries distributed nationwide by Target due to potential Listeria monocytogenes contamination.
Product
Good & Gather Organic cherries & berries fruit blend. Blueberries, dark sweet pitted cherries, tart pitted cherries & Strawberry slices. Net Wt 32 oz (2 lb) 907g, UPC 0 85239-04782 8. Keep Frozen. Distributed by Target Corporation Minneapolis, MN 55403
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1293-2023·2023-07-26
Organic Asian Chopped Salad Kits Recalled for Undeclared Milk and Egg
Braga Fresh Foods is recalling 673 cases of 365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits due to undeclared milk and egg allergens. Consumers with allergies to these allergens should not consume these products.
Product
365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits 12 oz plastic bags 9 bags per case UPC: 9948246932 Item#: 9770522
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1266-2023·2023-07-26
Good & Gather Mango Strawberry Blend recalled for Listeria contamination risk
Target's Good & Gather Mango Strawberry Blend is being recalled nationwide due to potential Listeria monocytogenes contamination. Listeria can cause serious illness.
Product
Good & Gather Mango Strawberry Blend. Whole Strawberries, Mango chunks & Pineapple Chunks. Net Wt 48 oz (3lb) 1.36kg, UPC 0 85239-04803 0. Keep Frozen. Dist. By Target Corp, Minneapolis, MN 55403
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2152-2023·2023-07-26
Cardiosave Rescue IABP Recalled Due to Unexpected Shutdown Risk
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to capacitor failures that may cause unexpected device shutdown. The devices may stop delivering therapy without warning.
Product
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2160-2023·2023-07-26
Medline Probe Cover Kits Recalled for Inadequate Seam Barriers
Medline is recalling 173,449 sterile probe cover kits due to inadequate seam barriers that may compromise sterility. The affected units were distributed worldwide between December 2017 and May 2023.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) ANGIOGRAPHY DRAPE PACK, Model Number 00-400305R; b) ANGIO HOLLAND PACK-LF, Model Number DYNJ0037936C; c) ANGIO HOLLAND PACK-LF, Model Number DYNJ0037936D; d) ANGIOGRAM, Model Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2183-2023·2023-07-26
Medline Ultrasound Probe Cover Kits Recalled for Seam Defects
Medline is recalling ultrasound probe cover kits containing sterile ultrasound gel due to an inadequate seam barrier. The defect may compromise sterility during diagnostic ultrasound procedures.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) IV SECUREMENT KIT, Model Number DYNDV2407A; b) USG IV START KIT, Model Number DYNDV2435; c) ULTRASOUND GUIDED IV START KIT, Model Number DYNDV2518; d) VI PACK, Model Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2156-2023·2023-07-26
FDA Recalls Medline Probe Cover Kits Due to Seam Defects
Medline is recalling probe cover kits used in diagnostic ultrasound procedures. The probe covers may have an inadequate barrier at the seams, which could compromise sterility during procedures.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) BLOCK PACK, Model Number DYNJ81722; b) PAIN BLOCK TRAY, Model Number DYNJRA0827A; c) PAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881; d) PAIN PREP TRAY W/PROBE COVER, Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2169-2023·2023-07-26
Medline Ultrasound Probe Cover Kits recalled for inadequate seam barrier
Medline is recalling 770,147 ultrasound probe cover kits worldwide due to inadequate barriers at the seams. The defect could allow contamination during diagnostic ultrasound procedures.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) FETAL SURGERY CDS-LF, Model Number CDS840214Q; b) MINOR PROCEDURE TRAY, Model Number DYNDA2418; c) CLOSUREFAST PROCEDURE PACK-LF, Model Number DYNJ0365463J; d) BARIATRIC PACK, Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2210-2023·2023-07-26
RET Distal Probe Recalled Due to Manufacturing Defect in DNA Sequences
FDA recalls RET Distal Probe due to manufacturing defect where DNA sequences used in production were inverted. The defect affects 61 units distributed in California, Florida, Ohio, and South Carolina and may impact diagnostic accuracy.
Product
RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2188-2023·2023-07-26
Medline Ultrasound Probe Cover Kits Recalled for Inadequate Seam Barriers
Medline Industries is recalling ultrasound probe cover kits due to inadequate barriers at the seams. The defect may allow contaminants to reach the patient during diagnostic ultrasound procedures.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: CHN OR DAVINCI PROSTATE, Model Number DYNJ902540N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2164-2023·2023-07-26
Medline Ultrasound Probe Cover Kits Recalled for Inadequate Seam Barrier
Medline is recalling ultrasound probe cover kits containing sterile gel due to inadequate barriers at the seams, which may fail to maintain sterility during diagnostic procedures.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) MHC VASCULAR HYBRID PK-LF, Model Number DYNJ53433K; b) VEIN SPECIALISTS PACK, Model Number DYNJ53616A; c) SUMMIT SKIN AND VEIN PACK, Model Number DYNJ54014B; d) VEIN PACK, Model Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2197-2023·2023-07-26
Medline Probe Cover Kits recalled for inadequate barrier at seams
Medline is recalling Probe Cover Kits (Model MNS10750A) used in diagnostic ultrasound procedures because the probe covers may have an inadequate barrier at the seams, potentially affecting protective effectiveness.
Product
Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: DIALYSIS ACCESSORY PACK W/O CATHETER, Model Number MNS10750A
Category
Medical Device
Distribution
Distributed nationwide