State

US Virgin Islands product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29851–29875 of 73776

ModerateFDA (Devices)·Z-1325-2020·2020-02-26
Nobel Biocare Abutment Screw Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 132 units of Abutment Screw Retrieval Instrument RP/WP/6.0 because a packaging sealing issue may compromise sterility during shelf life.
Product
Abutment Screw Retrieval Instrument RP/WP/6.0 - Product Usage: The instruments for abutment screw retrieval can be used if an abutment screw is broken and a part of the screw is left inside the implant screw channel. If the implant thread needs to be cleaned before placing a new…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1284-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Packaging Integrity Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 1 36 VIOLET GS-21, Item Code CL925 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1256-2020·2020-02-26
Edan iT20 Telemetry Transmitter Recalled for Uncleared Function
Edan Diagnostics is recalling 7 iT20 telemetry transmitters because they include a function not cleared by the U.S. FDA.
Product
EDAN Telemetry Transmitter, Model iT20 - Product Usage: The iT20 telemetry transmitter is intended to be used in clinical divisions of hospital environments, including CCU and general wards (as Cardiology Dept.)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1243-2020·2020-02-26
Arrow Central Venous Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc is recalling 140 units of Central Venous Catheterization Kits because the product lidstock contains the incorrect expiration date.
Product
Arrow Central Venous Catheterization Kit ASK-04200-UPM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1292-2020·2020-02-26
Recall of Polysorb Sutures Due to Potential Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 6-0 18" UNDYED SS-24 D/A, Item Code L2752K - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0770-2020·2020-02-26
Suja Organic Ginger Bliss Smoothie Recalled for Unapproved Herbicide
Suja Life LLC is recalling 9,005 bottles of Organic Ginger Bliss Fruit + Veggie Smoothie because raw flax material contained an unapproved herbicide.
Product
Suja Organic Ginger Bliss Fruit + Veggie Smoothie, 12 oz. UPC: 81861702236
Category
Food
Distribution
20 states
ModerateFDA (Devices)·Z-1281-2020·2020-02-26
Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 0 36 VIOLET GS-24, Item Code CL914 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1302-2020·2020-02-26
Nobel Biocare Recalls Guided Start Drills Due to Sterility Concerns
Nobel Biocare is recalling Guided Start Drills because a packaging sealing issue may compromise the sterility of the devices during their shelf life.
Product
Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered Drills) are used for preparing osteotomies for the specific related implants
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1300-2020·2020-02-26
Biosyn Monofilament Absorbable Suture Recalled for Packaging Integrity Issues
FDA is recalling Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23 due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Biosyn Monofilament Absorbable Suture 6/0 30" VIOLET CV-23, Item Code UM201
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1291-2020·2020-02-26
Polysorb Suture Recalled for Potential Packaging Integrity Issues
Covidien LLC is recalling Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 6/0 12"" VL SS-24 D/A, Item Code L1742K - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1299-2020·2020-02-26
Polysorb Suture Recalled for Potential Packaging Integrity Issues
Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 2/0 30"VIOLET GU-46, Item Code UL878 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1251-2020·2020-02-26
Arrow Epidural Catheterization Component Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 540 units of the Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 because the product lidstock contains the incorrect expiration date.
Product
Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1294-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Potential Packaging Integrity Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture UD 3/0 30 P-14, Item Code SL5679 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1287-2020·2020-02-26
FDA Recalls Polysorb Braided Absorbable Sutures Due to Packaging Integrity Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may compromise the sterility barrier.
Product
Polysorb Braided Absorbable Suture 0 VIOLET 30" V-20, Item Code GL124 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0771-2020·2020-02-26
Suja Organic Mango Mojito Smoothie Recalled for Unapproved Herbicide
Suja Life LLC is recalling 6,817 bottles of Organic Mango Mojito Fruit + Veggie Smoothie due to the presence of an unapproved herbicide in raw flax material.
Product
Suja Organic Mango Mojito Fruit + Veggie Smoothie, 12 oz. UPC: 81861702240
Category
Food
Distribution
20 states
ModerateFDA (Devices)·Z-1330-2020·2020-02-26
Mindray DP-30 Ultrasound Systems Recalled for Incorrect Needle-Guide Display
Mindray is recalling 53 DP-30 ultrasound systems and 18 USB drives because the devices display an incorrect needle-guide bracket when used with a specific transducer.
Product
DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic Diagnostic Imaging System is applicable for adults, pregnant women, pediatric patients and neonates. It is intended for use in fetal, abdominal, pediatric, small…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1265-2020·2020-02-26
Abbott i-STAT G3+ Cartridge Recalled for Lack of Clinical Evidence
Abbott Point of Care is recalling i-STAT G3+ blue cartridges because it lacks sufficient clinical evidence to characterize their performance.
Product
i-STAT G3+ cartridge (blue), List No. 03P78-50, UDI (01) 00054749002283 - Product Usage: The i-STAT G3+ cartridge may be used for the quantitative measurement of pH, pCO2, and pO2 in venous, arterial or capillary whole blood.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1285-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Potential Packaging Integrity Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact the humidity or sterility barrier.
Product
Polysorb Braided Absorbable Suture 2-0 UNDYED 36" GS-21, Item Code CL953 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1288-2020·2020-02-26
FDA Recalls Polysorb Sutures Due to Potential Sterility Barrier Issues
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise the sterility barrier.
Product
Polysorb Braided Absorbable Suture 2/0 UNDYED 30" V-30 (75CM), Item Code GL228 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1246-2020·2020-02-26
Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 160 units of the Arrow Epidural Catheterization Kit (YC-02220) because the product lidstock contains the incorrect expiration date.
Product
Arrow EPIDURAL CATHETERIZATION KIT YC-02220
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1320-2020·2020-02-26
Nobel Biocare Implant Retrieval Instruments Recalled for Sterility Concerns
Nobel Biocare is recalling 526 Implant Retrieval Instruments because a packaging sealing issue may compromise sterility during shelf life.
Product
Implant Retrieval Instrument CC RP & Tri Ch Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0731-2020·2020-02-26
CSM Bakery Products Recalls Cinnabon Cream Cheese Frosting Due to Plastic Contamination
CSM Bakery Products is recalling Cinnabon Cream Cheese Frosting because pieces of plastic polymer were introduced into the sugar system.
Product
22.5 lb. cases of 24 15 oz pouches CINNABON CREAM CHEESE FROSTING, MDM # 10236082, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1245-2020·2020-02-26
Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc. is recalling 870 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Product
Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0726-2020·2020-02-26
CSM Bakery Products Recalls Pink Decorating Buttercreme Frosting Due to Plastic Contamination
CSM Bakery Products is recalling 14 lb. pails of Pink Decorating Buttercreme Frosting because pieces of plastic polymer were introduced into the sugar system.
Product
14 lb. pail PINK DECORATING BUTTERCREME FROSTING, MDM # 10202860, Manufactured by Brill Inc. Tucker, GA 30084 1 866 982 7455 OR BRILLINC.COM
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1247-2020·2020-02-26
Arrow Epidural Catheterization Kit Recalled for Incorrect Expiration Date
Arrow International Inc is recalling 1,760 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Product
Arrow EPIDURAL CATHETERIZATION KIT JH-05500
Category
Medical Device
Distribution
Distributed nationwide