State

US Virgin Islands product recalls

73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17151–17175 of 73396

HighFDA (Devices)·Z-1074-2023·2023-02-15
Sterile Procedural Trays Recalled Due to Blade Packaging Puncture Hazard
Medline Industries is recalling multiple sterile procedural trays because blades within the kits can puncture the outer foil packaging. The products were distributed worldwide.
Product
Sterile Procedural Trays, labeled as the following: a. LAPAROTOMY CDS-LF b. LAPAROSCOPY CDS-LF c. BASIC LAPAROSCOPY CDS d. LAPAROSCOPY CDS-LF e. GENERAL LAPAROSCOPY PROCEDURE f. LAP CHOLE CDS g. COLO-RECTAL CDS-LF h. MAJOR PROCEDURE-LF i. HYPOSPADIUS CDS j. LAPAROSCOPY-GENERAL…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1071-2023·2023-02-15
Medline Sterile Procedural Trays Recalled Due to Blade Puncture Risk
Medline Industries is recalling sterile procedural trays (Rhinoplasty Pack, OSC Otology Pack-LF, and Rhyzotomy) distributed worldwide because sterile blades within the kits may puncture the outer foil layer of sterile packaging, potentially compromising sterility.
Product
Sterile Procedural Trays, labeled as the following: a. RHINOPLASTY PACK b. OSC OTOLOGY PACK-LF c. RHYZOTOMY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1082-2023·2023-02-15
Sterile Procedural Trays recalled due to potential sterile packaging puncture
Medline Industries is recalling Sterile Procedural Trays (IM NAIL) because sterile blades may puncture the outer foil layer of sterile packaging, potentially compromising sterility. No illnesses or injuries have been reported.
Product
Sterile Procedural Trays, labeled as the following: IM NAIL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2023·2023-02-15
Medline Procedural Trays Recalled for Blade Packaging Risk
Medline Industries is recalling Ambulatory Mini Pack sterile procedural trays because blades within the kits may puncture the outer sterile packaging, potentially compromising sterility.
Product
Sterile Procedural Trays, labeled as the following: AMBULATORY MINI PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1086-2023·2023-02-15
Sterile Procedural Trays Recalled Due to Potential Blade Packaging Puncture
Medline Industries is recalling sterile procedural trays because blades within the kits may puncture the outer foil packaging, potentially compromising sterility.
Product
Sterile Procedural Trays, labeled as the following: DR MOTT DRAPE PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1085-2023·2023-02-15
Sterile Procedural Trays Recalled Due to Blade Puncture Risk
Medline Industries is recalling Sterile Procedural Trays (LS MS PACK) because the sterile blade inside can potentially puncture the outer packaging layer, compromising sterility.
Product
Sterile Procedural Trays, labeled as the following: LS MS PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1080-2023·2023-02-15
Medline Sterile Procedural Trays Recalled Due to Blade Puncture Risk
Medline recalls sterile surgical trays (Universal Plastic and Knee Arthroscopy Pack) because sterile blades can puncture the outer foil packaging, potentially compromising sterility.
Product
Sterile Procedural Trays, labeled as the following: a. UNIVERSAL PLASTIC b. KNEE ARTHROSCOPY PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1060-2023·2023-02-15
Medline Sterile Procedural Trays Recalled for Packaging Puncture Risk
Medline Industries is recalling ANCILLARY PACK-LF sterile procedural trays because sterile blades in the kits may puncture the outer foil layer of sterile packaging, potentially compromising the sterility of the contents.
Product
ANCILLARY PACK-LF. Sterile Procedural Tray.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1068-2023·2023-02-15
Sterile Procedural Trays Recalled Due to Blade Package Puncture Risk
Medline sterile procedural trays are recalled because sterile blades within the kits can puncture the outer foil packaging, potentially compromising sterility. 622 cases (1,619 units) have been distributed worldwide.
Product
Sterile Procedural Trays, labeled as the following: a. PORT/TRACH INSERTION CDS-3 b. RESIDENT DERM SURG PACK c. THROMBECTOMY PACK-LF d. AV FISTULA PACK e. AV SHUNT PACK-LF f. RR-VP SHUNT PACK-LF g. VEIN HARVESTING PACK-LF h. AV FISTULA PACK-LF i. PK, GEN-BARIATRIC j.…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V087000·2023-02-15
2021-2024 Peterbilt and Kenworth trucks recalled for brake pedal disconnection
PACCAR is recalling 8,008 Kenworth and Peterbilt trucks (2021-2024) because the brake pedal plunger may disconnect during rapid brake release, causing complete service brake failure and crash risk.
Product
PETERBILT — PETERBILT, KENWORTH 537, 536, T380, 548
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1095-2023·2023-02-15
Sterile Ophthalmic Procedure Trays Recalled for Packaging Integrity Risk
Medline Industries is recalling sterile ophthalmic procedure trays because blades in the kits can puncture the outer foil packaging, potentially compromising sterility. The recall affects 1,200 units distributed worldwide.
Product
Sterile Procedural Trays, labeled as the following: a. BASIC EYE PACK-LF b. VITRECTOMY PACK-LF c. EYE PACK-EAST-LF d. OSC OCULAR PLASTIC PACK-LF e. EYE PACK f. OCULOPLASTIC PACK g. EYE PLASTIC PACK h. PLASTIC EYE PACK i. DR H BLEPH PACK j. BLEPH PACK k.…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V086000·2023-02-15
Audi Recalls 2009-2015 Q7 Models Due to Incorrect Weight Rating Label
Audi is recalling 2009-2015 Q7 vehicles because an incorrect Gross Axle Weight Rating on the certification label may allow the vehicle to be overloaded, increasing crash risk.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1108-2023·2023-02-15
Vascular Covered Stent Recalled Due to Deployment Failure Risk
Bard Peripheral Vascular Inc is recalling approximately 10,815 Covera Vascular Covered Stent devices due to poor slide block bonding that may prevent proper deployment during vascular procedures.
Product
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a nitinol stent framework. The inner lumen of the covered stent is carbon impregnated.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1107-2023·2023-02-15
Surgical instrument tracker recalled for structural failure during use
Trackx Technology is recalling 464 units of its Insight Base Modular Instrument Tracker because the device breaks and falls off from surgical instruments during procedures. No injuries have been reported.
Product
TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model #605-3TX, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0264-2023·2023-02-15
Ohm Sanitizer Spray Recalled Due to Chemical Contamination
Urban Electric Power is recalling Ohm Sanitizer Spray nationwide because FDA analysis found the product contains acetaldehyde and acetal above specification limits.
Product
Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1061-2023·2023-02-15
Sterile Trach Pack procedure kits recalled due to blade puncture risk
Medline Industries is recalling TRACH PACK sterile procedure kits because sterile blades within the kits can puncture the outer foil packaging, potentially compromising product sterility.
Product
TRACH PACK. Sterile Procedural Tray.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V085000·2023-02-15
Tesla Model S Full Self-Driving Beta Software Recall for Unsafe Driving
Tesla's Full Self-Driving Beta software in 2020 Model S and other models may cause vehicles to drive unsafely through intersections or ignore speed limits. Tesla will provide a free over-the-air software fix.
Product
TESLA — TESLA MODEL X, MODEL S, MODEL 3, MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1072-2023·2023-02-15
Medline Sterile Procedural Trays Recalled for Potential Packaging Puncture Risk
Medline Industries is recalling approximately 27,563 units of sterile procedural trays used in surgery because sterile blades may puncture the outer foil packaging layer, potentially compromising sterility.
Product
Sterile Procedural Trays, labeled as the following: a. EAR CDS-LF b. SINUS CDS-1 c. ZALE FESS CDS d. ZALE OTOLOGY CDS e. ZALE HEAD & NECK CDS f. CUH PARA/THYROIDECTOMY CDS g. CAM ENDOSCOPIC SINUS/SEPTO CDS h. HEAD AND NECK CDS i. HEAD AND NECK CDS-LF j. NASAL k. ENT SET UP CDS…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1100-2023·2023-02-15
Precision Delivery Sets recalled due to potential tubing detachment
Quest Medical recalls Precision Delivery Sets (models PD06F and PDT05CV2) due to tubing that may detach, potentially causing patient infection. Approximately 13,900 units were distributed nationwide.
Product
Precision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set with Trifurcated Luer, REF: PDT05CV2
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V084000·2023-02-15
Audi Recalls 2022-2023 S8 and A8 Models for Air Bag Defect
Audi is recalling 2022-2023 S8 and A8 vehicles because the front-passenger air bag may deploy with excessive force, increasing injury risk.
Product
AUDI — AUDI S8, A8
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1096-2023·2023-02-15
Medline Sterile Procedural Trays Recalled Due to Packaging Puncture Risk
Medline recalls sterile procedural trays because blades may puncture the foil packaging, potentially compromising sterility. The recall affects over 227,000 units distributed worldwide.
Product
Sterile Procedural Trays, labeled as the following: a. SPINAL b. SPINE CDS c. TOTAL ORTHO CDS d. TOTAL KNEE CDS e. CDS HIP-LF f. KNEE TOTAL PACK-LF g. EXTREMITY CDS h. SHOULDER ARTHRO CDS i. GLENNON EXTREMITY CDS j. KNEE ARTHROSCOPY k. TOTAL KNEE l. TOTAL HIP REPLACEMENT m.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1063-2023·2023-02-15
Medline Sterile Procedural Trays recalled due to packaging defect risk
Medline Industries is recalling sterile procedural trays because sterile blades within the kits may puncture the outer foil sterile packaging, potentially compromising sterility.
Product
Sterile Procedural Tray, labeled as the following: a. PAIN SERVICE PACK-LF; b. LOCAL BASIC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1094-2023·2023-02-15
Sterile Procedural Trays Recalled Due to Blade Puncture Risk
MEDLINE INDUSTRIES is recalling sterile surgical trays used in robotic and laparoscopic procedures because blades within the kits can puncture the outer foil packaging. The recall affects 1,212 cases (2,101 units) distributed worldwide.
Product
Sterile Procedural Trays, labeled as the following: a. CELEBRATION ROBOTIC CDS b. DAVINCI CDS UCC-LF c. ROBOTICS PACK-LF d. ROBOTICS PACK-LF e. ROBOTIC PACK f. PELVISCOPY PACK-LF g. CUSTOM LITHOTOMY ROBOT PACK h. PERI GYN PACK i. ROBOTICS PACK j. LAP HYSTO PACK k.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0348-2023·2023-02-15
Sour Patch Kids Watermelon Jelly Beans Recalled for Undeclared Yellow No. 5
Mondelez is recalling Sour Patch Kids Watermelon Jelly Beans due to undeclared FD&C Yellow No. 5, an allergen that could harm consumers with sensitivities to this dye.
Product
Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UPC: 0 70462 00719 0 24 bags per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1093-2023·2023-02-15
Sterile Surgical Trays Recalled for Blade Puncture Risk
Medline Industries recalls sterile surgical procedural trays because blades inside could puncture the outer sterile packaging, potentially compromising kit sterility.
Product
Sterile Procedural Trays, labeled as the following: a. GYN ABD CDS b. LAVH PROCEDURE c. TAH CDS d. CUH LITHOTOMY CDS e. LAVH CDS f. GROTH VAGINAL CDS g. MAJOR LITHOTOMY h. MAJOR VAGINAL HARPER PACK-LF i. VAG. HYST TRAY-LF j. VAGINAL HYSTERECTOMY PACK-LF k.…
Category
Medical Device
Distribution
Distributed nationwide