State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46651–46675 of 73987

SevereFDA (Drugs)·D-1500-2016·2016-09-21
Hospira Recalls Dobutamine Injection Vials Due to Discoloration and Particulates
Hospira Inc. is recalling 24,000 vials of Dobutamine Injection due to reports of product discoloration and particulates. The affected lot was distributed nationwide and to Puerto Rico and the Bahamas.
Product
DOBUTamine Injection, USP 250 mg/20 mL, 20 mL Vial, For IV Use Only, Must be Diluted Prior to Use, (12.5 mg per mL), Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2025-20
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2808-2016·2016-09-21
ICU Medical Recalls Transpac IV Monitoring Kits Due to Leak Risk
ICU Medical is recalling specific Transpac IV Monitoring Kits because of a potential for leaks in the SafeSet Reservoir and blood sampling components.
Product
Transpac IV Monitoring Kit with 2 SafeSet Blood Sampling Ports, 60" TUBING, Disposable Transducer, 3 ML Intraflo Flush, Macrodrip (Pole Mount), Item No. 42619-08 Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2786-2016·2016-09-21
Howmedica Recalls AccuLIF PL Spinal Cages Due to Height Reduction
Howmedica Osteonics Corp. is recalling AccuLIF PL spinal cages because some implants have shown a reduction in height greater than 1 mm after surgery.
Product
AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2198-2016·2016-09-21
National Frozen Foods Recalls Mixed Vegetables for Listeria Risk
National Frozen Foods Corporation is recalling IQF Mixed Vegetables due to potential Listeria monocytogenes contamination. The products were distributed in the US, Canada, and Japan.
Product
Not Ready to Eat, IQF Mixed Vegetables. Products' labels contains Cooking Instructions. Products are sold under various brands and various net weight. Heinz Mixed Vegetables 02521-39698 14902521396989 4902521396982 12/1 KG Heinz Mixed Vegetables 02521-39698…
Category
Food
Distribution
Distributed nationwide
HighCPSC·16268·2016-09-21
Lenny Lamb Buckle Onbu Infant Carriers Recalled for Fall Hazard
Lenny Lamb is recalling Buckle Onbu infant carriers because missing internal stitching creates a fall hazard for children. No injuries have been reported.
Product
Buckle Onbu infant carriers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2820-2016·2016-09-21
ICU Medical Recalls SafeSet Reservoir Kits Due to Leak Risk
ICU Medical is recalling 20 units of Bifurcated SafeSet Kits with 03mL Flush Devices due to a potential for leaks.
Product
Bifurcated SafeSet Kit with 03mL Flush Device, Item No. 46091-75 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2179-2016·2016-09-21
Mars Recalls Combos Pizzeria Pretzels for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Pizzeria Pretzels due to potential undeclared peanut residue. The recall affects 183,678 cases distributed nationwide and in foreign markets.
Product
COMBOS PIZZERIA PRETZEL - Net Wt. 1.80 OZ (51 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419714751
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2165-2016·2016-09-21
Mars Recalls Combos Cheddar Cheese Pretzels for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Cheddar Cheese Pretzels due to the potential for undeclared peanut residue.
Product
COMBOS CHEDDAR CHEESE PRETZEL Net Wt. 6.30 oz (178.6 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419420058
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2171-2016·2016-09-21
Mars Recalls Combos Cheddar Cheese Pretels for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Cheddar Cheese Pretels due to potential undeclared peanut residue. The recall affects 183,678 cases distributed nationwide and abroad.
Product
COMBOS SNACKS CHEDDAR CHEESE PRETZEL - 15 OZ - Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419780480
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2805-2016·2016-09-21
ICU Medical Recalls Transpac IV Monitoring Kits Due to Leak Risk
ICU Medical is recalling 420 Transpac IV Monitoring Kits with SafeSet Reservoirs due to a potential leak. The affected units were distributed nationwide in the US.
Product
Transpac IV Monitoring Kit with SafeSet 84inch Arterial Pressure Tubing, Reservoir, Squeeze Flush and 2 Needleless Valves, Item No. 011-42646-66 Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2122-2016·2016-09-21
Hostess Donettes Glazed Mini Donuts Recalled for Unlabeled Peanut Allergen
Hostess Brands is recalling Donettes Glazed Mini Donuts because the flour used contains peanut allergen, which is not listed on the label.
Product
Hostess Donettes Glazed Mini Donuts, packaged in 9-17-ct and 6-17-ct bags of mini donuts, net wt. 10.50oz, UPC 888109110659;the most responsible firm name on the label is Hostess Brands, LLC, Kansas City, MO 64141.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2119-2016·2016-09-21
Hostess Donettes Powdered Mini Donuts Recalled for Peanut Allergen Mislabeling
Hostess Brands is recalling Donettes Powdered Mini Donuts because they were manufactured with flour containing peanut allergen but are not labeled to contain peanuts.
Product
Hostess Donettes Powdered Mini Donuts, packaged in 9ct and 6-20ct bags of mini donuts, net wt. 10.5oz, UPC 888109150044; packaged in 9ct bag of mini donuts, net wt. 13.16oz, UPC 888109110246; packaged in 6ct single serve packages, net wt. 3oz, UPC 888109050047; the most…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2796-2016·2016-09-21
Merge Healthcare Recalls RadSuite Software Due to Missing Studies
Merge Healthcare is recalling RadSuite software versions where studies may be missing from archives before watermarking.
Product
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2799-2016·2016-09-21
Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Data Mismatch
Siemens Healthcare Diagnostics Inc is recalling 6,786 RAPIDPoint 500 Blood Gas Analyzers because patient names may be printed with data from a different patient.
Product
Siemens RAPIDPoint 500 Blood Gas Analyzer Siemens Material Number (SMN): 10492730, 10696855, 10696857, 10697306
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2176-2016·2016-09-21
Mars Recalls Combos Snacks Cheddar Cheese Pretzels for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Snacks Cheddar Cheese Pretzels due to potential undeclared peanut residue.
Product
COMBOS SNACKS CHEDDAR CHEESE PRETZEL - Net Wt. 1.80 OZ (51 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA 41419714713
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2168-2016·2016-09-21
Mars Recalls Combos Pepperoni Crackers for Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Pepperoni Crackers due to potential undeclared peanut residue. The recall covers 183,678 cases distributed nationwide and abroad.
Product
COMBOS PEPPERONI CRACKER - Net Wt. 1.70 oz. (48.2 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419420089
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2813-2016·2016-09-21
ICU Medical Recalls Transpac IV Monitoring Kits Due to Leak Risk
ICU Medical is recalling 90 units of Transpac IV Trifurcated Monitoring Kits due to a potential for leaks in the SafeSet Reservoir and blood sampling components.
Product
Transpac IV Trifurcated Monitoring Kit with 84" SafeSet Reservoir, 03 ml Squeeze Flush and Needleless Valves, Item No. 42650-66 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2802-2016·2016-09-21
Siemens RAPIDLab 1260 Blood Gas Analyzer Recalled for Data Mismatch
Siemens is recalling 114 RAPIDLab 1260 Blood Gas Analyzers because patient names may be printed with data from different patients.
Product
RAPIDLab 1260 Blood Gas Analyzer Siemens Material Number (SMN): 10321846, 10491394
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2169-2016·2016-09-21
Mars Recalls Combos Pretzels for Potential Undeclared Peanut Residue
Mars Chocolate North America is recalling Combos Buffalo Blue Cheese Pretzels due to potential undeclared peanut residue.
Product
COMBOS BUFFALO BLUE CHEESE PRETZEL Net Wt.6.30 oz (178.6 g)Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 4141420119
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2806-2016·2016-09-21
ICU Medical Recalls Transpac IV Trifurcated Kits Due to Leak Risk
ICU Medical is recalling 250 units of Transpac IV Trifurcated Kits due to a potential leak in the SafeSet Reservoir and blood sampling components.
Product
Transpac IV Trifurcated Kit With Safeset Reservoir And 2 Blood Sampling Ports, 84 inch Tubing, 3 3 ml Intraflo Flushes, 3 Disposable Transducers, Macrodrip, Item No. 42500-04 Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2825-2016·2016-09-21
ICU Medical Recalls Transpac IV Transducer Kits Due to Leak Risk
ICU Medical is recalling 140 units of TP4 Kits with SafeSet Reservoirs due to a potential for leaks. The affected medical devices were distributed nationwide.
Product
TP4 Kit with 10cc SafeSet Reservoir, Needleless Valve, Filter Millex and Admin Set, Item No. 46104-65 Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2178-2016·2016-09-21
Mars Recalls Combos Cheddar Cheese Crackers for Undeclared Peanut Residue
Mars Chocolate North America is recalling specific Combos Cheddar Cheese Crackers due to potential undeclared peanut residue. Consumers should check their packages for the listed codes.
Product
COMBOS SNACKS CHEDDAR CHEESE CRACKER - Net. Wt. 1.70 oz (48.2g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419714744
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2789-2016·2016-09-21
Stryker Patella Assembly Instrument Recalled for Component Disassociation Risk
Stryker Howmedica Osteonics is recalling 2,039 units of the Scorpio Patella Assembly Instrument because press-fit failures could cause clamping components and pins to disassociate.
Product
Stryker Orthopaedics Patella Assembly Instrument, REF 3182-1000, Non-Sterile, NDC (01) 07613327215854 (10) The Scorpio Patella Assembly Instrument is used during total knee replacement surgery for the implantation of Scorpio Patella implant components. The device functions to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2113-2016·2016-09-21
Hostess Chocodile Twinkies Recalled for Unlabeled Peanut Allergen
Hostess Brands is recalling Chocodile Twinkies because the product was manufactured with flour containing peanut allergen but is not labeled to contain peanuts.
Product
Hostess Chocodile Twinkies, chocolate covered sponge cake with creamy filling, packaged in 9-ct multi-packs of individual cakes, net wt. 13.02 oz (396 g), UPC 888109110499; and 6-ct. single serving fun size snack packs, individual pack net wt. 2.89 oz (82 g), UPC 888109010492.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2788-2016·2016-09-21
Howmedica Recalls AccuLIF PL Cages Due to Height Reduction
Howmedica Osteonics Corp. is recalling AccuLIF PL Cages because some implants have shown a reduction in height greater than 1 mm.
Product
AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an…
Category
Medical Device
Distribution
Distributed nationwide