State

US Virgin Islands product recalls

73,388 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: 39
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 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21051–21075 of 73565

HighFDA (Devices)·Z-0931-2022·2022-04-20
Siemens Atellica CH Lithium reagent recalled for potential reagent carryover
Siemens Healthcare Diagnostics recalls approximately 2,158 units of Atellica CH Lithium_2 reagent (Lot Numbers 110108, 110185, 110238, 110302) due to potential for reagent carryover affecting quality control results, patient samples, and calibrator results.
Product
Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0928-2022·2022-04-20
Siemens Atellica CH Calcium_2 Reagent Carryover Recall
Siemens is recalling Atellica CH Calcium_2 diagnostic reagent due to potential reagent carryover that could impact quality control, patient samples, and calibrator results. The recall affects approximately 2,395 units distributed globally and in the US.
Product
Atellica CH Calcium_2 (CA_2), Siemens Material Number 11097644
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0983-2022·2022-04-20
Kroger Buttermilk Pancake & Waffle Mix Recalled for Foreign Material Contamination
Kroger Buttermilk Pancake & Waffle Mix with specific lot codes may contain foreign materials. Consumers who purchased this product should not use it.
Product
Item # 714-0706, Kroger Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 11110 88219 6.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0934-2022·2022-04-20
Surgical Head Fixation Device Mount Clamp Assembly Deflection Recall
Deerfield Imaging recalls the Trumpf Mount Clamp Assembly component used in surgical head fixation devices. The clamp may deflect during use and become difficult to loosen after procedures, potentially requiring surgical intervention.
Product
Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation device, models #119629-000 and #119630-000, which are used with ORT400 operating room tables.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0910-2022·2022-04-20
Orthopedic Surgical Instrument Kit Recalled for Improper Driver Fit
The Nextra Hammertoe Correction System surgical kit is being recalled due to an oversized driver that cannot properly connect to and remove from the implant. This defect can delay surgery.
Product
Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: NX-4532K Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0985-2022·2022-04-20
Krusteaz Buttermilk Pancake Mix Product Recalled Nationwide for Foreign Materials
Krusteaz Buttermilk Pancake Mix (Lot code KX2066, best-by 3/6/2024) is being recalled nationwide due to foreign materials. Consumers should not consume this product.
Product
Item # 721-0200, Krusteaz Buttermilk Pancake Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 41449 00110 4.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0990-2022·2022-04-20
Gordon Choice Yellow Cake Mix nationwide recall for foreign materials
Continental Mills is recalling Gordon Choice Yellow Cake Mix (lot KX2066) nationwide due to the presence of foreign materials. The recall was voluntarily initiated on March 10, 2022.
Product
Item # 744-4875, Gordon Choice Yellow Cake Mix. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 24575 5
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0935-2022·2022-04-20
ECG Electrode Set Fails Electrical Safety, May Prevent Effective Defibrillation
Graphic Controls' CLARAVUE pediatric electrode set fails electrical safety standards. The device may not deliver adequate charge during defibrillation, potentially rendering emergency treatment ineffective.
Product
CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0943-2022·2022-04-20
Ventilator trolley mounting brackets can detach and cause device to fall
The mounting brackets on Breas Ventilator Trolleys can become detached, allowing ventilators to fall. This poses an injury risk to people near the equipment.
Product
Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS ventilator models Article no 007384
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0921-2022·2022-04-20
Abbott Vascular 20/30 Indeflator Recalled for Leaks and Connection Failures
Abbott Vascular recalls 20/30 Indeflator medical devices due to increased complaints of leaks and loose connections. The recall affects 17 product lots distributed nationwide and internationally.
Product
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0941-2022·2022-04-20
Medline Laryngeal Masks recalled due to potential cuff disconnection
Medline Industries is recalling approximately 8,990 cases of Standard PVC Laryngeal Masks distributed nationwide because the mask cuff may disconnect from the breathing tube.
Product
Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V267000·2022-04-20
Certain BMW Vehicles: Sunroof May Close Without Key Fob Present
BMW is recalling 2019-2023 X5, X6, X7, and 4 Series vehicles because the sunroof may close without the key fob inside, creating injury risk. Dealers will reprogram the control unit free of charge.
Product
BMW — BMW X7, X5, X6, M440I
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0936-2022·2022-04-20
Recalled CLARAVUE Pre-wired Electrode Set May Fail During Defibrillation
Graphic Controls is recalling CLARAVUE Pre-wired Electrode sets because they fail to meet electrical safety specifications for defibrillators, potentially delivering inadequate charge during emergency treatment.
Product
CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600 US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0991-2022·2022-04-20
Fish Breader Recalled Nationwide for Foreign Material Contamination
Continental Mills is recalling Gordon Choice Southern Style Fish Breader (Lot KX2065) nationwide due to the presence of foreign materials. Consumers should not consume this product and should return it to the place of purchase.
Product
Item # 744-4930, Gordon Choice Southern Style Fish Breader. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 75622 0.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0912-2022·2022-04-20
Orthopedic surgical hammertoe instrument recalled for improper component sizing
Nextremity Solutions is recalling the Nextra Hammertoe Correction System due to an oversized driver component that makes it difficult to properly connect and remove during surgery.
Product
Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: NX-3532K Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0987-2022·2022-04-20
IHOP Pancake Mix Recalled Nationwide for Foreign Material Contamination
Continental Mills is recalling 240 cases of IHOP Pancake Mix (Item #743-0278) nationwide due to the presence of foreign materials. Affected lots are KX2062 and KX2063 with a best-by date of 9/1/2022.
Product
Item # 743-0278, IHOP Pancake. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 41449 47540 0.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0939-2022·2022-04-20
Cardiac electrode fails electrical safety test; defibrillation may not work
The CLARAVUE Pre-wired Electrode does not meet electrical safety standards for defibrillators. It may not deliver effective electrical charge during emergency defibrillation.
Product
CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0914-2022·2022-04-20
Orthopedic surgical driver oversized, affecting hammertoe correction
Nextremity Solutions is recalling the Nextra Hammertoe Correction System Driver (SKU: NX-DR) due to oversizing at the proximal end, which impairs connection and removal from the implant, causing surgical delays. The defect affects 239 units distributed in the US, Japan, and the Netherlands.
Product
Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0923-2022·2022-04-20
Abbott Vascular Cardiovascular Device Recalled for Leaks and Loose Connections
Abbott Vascular is recalling the 20/30 Priority Pack w/COPILOT device due to an increase in complaints of leaks and loose connections. The recall affects 131 lots distributed nationwide and internationally.
Product
20/30 Priority Pack w/COPILOT - REF 1003327 WPL2122272-01 (2019-03-01)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0986-2022·2022-04-20
Krusteaz Pro Buttermilk Pancake Mix Recalled Nationwide for Foreign Materials
Krusteaz Pro Buttermilk Pancake Mix is being recalled due to potential foreign materials. Approximately 970 cases with specific lot codes were distributed nationwide.
Product
Item # 731-0120, Krusteaz Pro Buttermilk Pancake Mix. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 41449 10180 4.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0906-2022·2022-04-20
Integra Universal Flexible Arm Recall: Internal Cable May Break
Integra LifeSciences is recalling the Universal Flexible Arm (part number REF 1362275) because excess tightening force can break the internal cable at the tip, rendering the device unusable.
Product
Integra Universal Flexible Arm part number REF 1362275
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0992-2022·2022-04-20
Tattooed Chef Plant-Based Sausage Breakfast Bowl Recalled for False Gluten-Free Claim
Ittella International recalls Tattooed Chef Plant-Based Sausage Breakfast Bowls nationwide due to an incorrect gluten-free claim on the container lid. The product contains wheat flour, which is correctly listed in the ingredients and allergen statement.
Product
Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 850015982569 Packed for: Tattooed Chef Paramount, CA 90723
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0769-2022·2022-04-20
Lansoprazole Delayed-Release Capsules Recalled for Out-of-Specification Dissolution
Preferred Pharmaceuticals is recalling certain lots of Lansoprazole Delayed-Release Capsules 15mg due to dissolution testing results that do not meet specifications. Approximately 791 bottles were distributed nationwide.
Product
Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0924-2022·2022-04-20
Abbott INDEFLATOR Plus 30 Device Recalled for Leaks and Connection Faults
Abbott Vascular is recalling INDEFLATOR Plus 30 balloon inflators due to increasing complaints of leaks and intermittent loose connections that could affect device function during medical procedures.
Product
INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V269000·2022-04-20
Daimler Trucks Recalls 2022 Western Star 4900 and 4700 for Seat Belt Defect
Daimler Trucks North America is recalling 2022 Western Star 4900 and 4700 trucks because seat belts may not be secured properly, increasing injury risk in crashes.
Product
WESTERN STAR — WESTERN STAR 4900, 4700
Category
Vehicle
Distribution
Distributed nationwide