State

US Virgin Islands product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19126–19150 of 73543

HighFDA (Devices)·Z-1604-2022·2022-08-31
Central Venous Catheter Kits Recalled for Potential Temperature Damage
McKesson Medical-Surgical is recalling Teleflex Arrow Central Venous Catheter Kits due to temperature excursions during storage and shipment. Exposure to higher temperatures may have reduced product effectiveness.
Product
TELEFLEX LLC Arrow Central Venous Catheter Kit 16, 18 Gauge Multi Lumen Model Number:CDC-45703-XP1A (Model Numbers # IPN035619, IPN036437, IPN922677)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1562-2022·2022-08-31
DeRoyal Limb Holders and Security Cuffs Buckle Webbing Strap Failure
DeRoyal is recalling specific limb holders and security cuffs due to improperly laced webbing straps that may slide loose, potentially compromising device security.
Product
DeRoyal limb holders: (1) DeRoyal Limb Holder, Wrist, Fixed, Quick Release, REF M8124; (2) DeRoyal Limb Holder, Ankle, Fixed, Quick Release, REF M8125; (3) DeRoyal Security Cuffs, Wrist and Ankle, Universal, REF M8136; and (4) DeRoyal Security Cuffs, Heavy Duty Vertical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1571-2022·2022-08-31
Vanta Clinician Programmer Application error prevents programming of implanted neurostimulators
The Vanta Clinician Programmer Application v2.0.2455 may display Error Code 1502, preventing users from programming Vanta implantable neurostimulators. The issue affects 2,920 downloaded software applications distributed worldwide.
Product
Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain therapy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1625-2022·2022-08-31
Surgical ophthalmic wicks recalled for potential effectiveness loss
McKesson Medical-Surgical Inc. is recalling Beaver-Visitec Ultracell surgical wicks due to facility temperature excursions during storage. Temperature exposure may have impacted product effectiveness, affecting units distributed nationwide between June and September 2021.
Product
BEAVER-VISITEC INTERNATIONAL, INC. Ultracell WICK, FENSTD PED 7MMX20MM(10/BX) BVRVIS Catalog #30316-C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1572-2022·2022-08-31
Enjoy Life Brownie Bites Recalled for Potential Hard Plastic Pieces
Enjoy Life Natural Brands is recalling Enjoy Life Brownie Bites Rich Chocolate (UPC 819597013290) due to potential hard plastic pieces in the product. No illnesses have been reported.
Product
Enjoy Life Brownie Bites Rich Chocolate, 4.76 oz UPC 819597013290
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2022·2022-08-31
B. Braun Gravity Mixing Container Recalled for Temperature Exposure
B. Braun EVA Gravity Mixing Container 1000 mL units may have been exposed to higher temperatures during storage prior to delivery, potentially affecting product effectiveness. Units distributed nationwide between June and September 2021 are affected.
Product
B. Braun EVA Gravity Mixing Container 1000 mL Model Number: 2112363
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1571-2022·2022-08-31
Enjoy Life Breakfast Ovals Recalled for Potential Hard Plastic Pieces
Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals (Berry Medley) are being recalled due to potential hard plastic contamination. Approximately 89,736 cases were distributed nationwide in the US and Canada.
Product
Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals Berry Medley, 8.8 oz (250g) UPC 819597012583 and 819597012712
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1629-2022·2022-08-31
Beckman Coulter Laboratory Reagents Recalled for Temperature-Related Effectiveness Loss
Beckman Coulter diagnostic reagents used in blood analysis systems were recalled after exposure to temperature excursions during storage and shipment. Products received between June and September 2021 may have reduced effectiveness.
Product
BECKMAN COULTER, INC. a. COULTER DxH Diff Pack REAGENT, DIFF PK FP DXHCOULTR, Catalog #628020. b. COULTER DxH Cleaner REAGENT, CLEANER FP DXH 10LCOULTR Catalog #628023. c. DxH 500 Series Lyse LYSE, VERSA SOL DXH 500 SERIES(0.5L/KT) Catalog # B36846. d. DxH 500…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1401-2022·2022-08-31
Jet Alert Tablets Recalled for Improper Storage Temperature Conditions
Jet Alert stimulant tablets distributed nationwide from April to June 2022 are being recalled due to improper storage temperature conditions that may affect product safety and efficacy.
Product
JET ALERT TABLET 30 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1372-2022·2022-08-31
Tylenol and Acetaminophen Products Recalled Due to Improper Storage
Family Dollar Stores is recalling multiple Tylenol and acetaminophen products due to CGMP deviations involving improper storage temperature conditions. Products were distributed nationwide through specific Family Dollar locations from April 30, 2022 through June 10, 2022.
Product
Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559; TYLENOL CHILD GRAPE 4 FL OZ SKU 901600 TYLENOL CHILD ORAL SUSPENSION CHERRY 4 FO 913104 TYLENOL INFANTS DROPS DF CHERRY 1OZ SKU 999108 TYLENOL PM CAPLET 24 CT SKU 900603 TYLENOL EXTRA STRENGTH CAPLET 24 CT SKU…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1579-2022·2022-08-31
Baxter Syringe Tip Caps Recalled for Potential Sterile Barrier Failure
Baxter Healthcare Corporation is recalling 168,390 units of DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier, creating a contamination risk.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1566-2022·2022-08-31
Enjoy Life Soft Baked Cookies recalled for hard plastic pieces
Enjoy Life Natural Brands is recalling Enjoy Life Soft Baked Cookies Monster (6 oz) due to potential hard plastic pieces. The recall affects 89,736 cases distributed nationwide in the US and Canada with best-by dates between 2/6/2023 and 3/3/2023.
Product
Enjoy Life Soft Baked Cookies Monster, 6 oz. UPC 819597013818
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1381-2022·2022-08-31
Family Dollar Oral Pain Relief Products Recalled for Improper Storage
Family Dollar recalled multiple oral pain relief products due to storage temperature deviations. The products were distributed to select Family Dollar stores from April 30, 2022 through June 10, 2022.
Product
ORAJEL GUM PAIN RELIEF GEL 0.125OZ SKU 903432 GOOD SENSE ORAL PAIN RELIEF 0.5OZ SKU 999543 ORAJEL ORAL PAIN 0.125 FL OZ SKU 912968 ORAJEL MOUTH SORE GEL 0.125 OZ SKU 999075 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1591-2022·2022-08-31
Perifix LOR Syringes Recalled Due to Temperature Exposure During Storage
Mckesson recalled 415 Perifix LOR syringes (Model 332152) distributed nationwide due to temperature excursions from June to August 2021 that may have affected product effectiveness. No illnesses have been reported.
Product
Perifix LOR Syringe Perifix 8 mL Pouch Luer Lock Tip Without Safety Model Number: 332152
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1431-2022·2022-08-31
Topical Skincare Products Recalled for Improper Storage Conditions
Family Dollar Stores is recalling three topical skincare products distributed nationwide due to storage condition violations in manufacturing.
Product
ST IVES BLKHD CLRNG GREEN TEA SCRUB 6 OZ SKU 2007787 AMBI EXFOLIATING WASH 5 OZ SKU 2097153 CC BLACKHEAD SCRUB 5 OZ SKU 2032021 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1632-2022·2022-08-31
Morrison Medical OB Kit Recalled Due to Temperature Excursion During Storage
Mckesson is recalling Morrison Medical OB Kits because facility temperature excursions may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
MORRISON MEDICAL Morrison Medical OB KIT, HARD PK SEALED W/CARDBOARD BX MORMED Catalog #0967NL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1594-2022·2022-08-31
Medical Device Recall: Wetfield Eraser Bipolar Hemostatic due to temperature exposure
McKesson is recalling Wetfield Eraser Bipolar Hemostatic devices that were exposed to elevated facility temperatures from June to August 2021 prior to delivery. This exposure may have impacted the devices' effectiveness.
Product
Wetfield Eraser Bipolar Hemostatic Eraser Wet-Field Eraser 23 Gauge Tapered Model Number: 221265
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1457-2022·2022-08-31
Mucinex FastMax Caplets Cold Flu Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Mucinex FastMax Caplets Cold Flu 4CT (SKU 903372) distributed nationwide from April to June 2022 due to improper storage temperature conditions.
Product
MUCINEX FASTMAX CAPLETS COLD FLU 4CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1563-2022·2022-08-31
Enjoy Life Soft Baked Cookies recalled for potential hard plastic pieces
Enjoy Life Natural Brands is recalling Soft Baked Chocolate Chip Cookies nationwide due to potential hard plastic contamination. Affected products have Best By dates from February to March 2023.
Product
Enjoy Life Soft Baked Cookies Chocolate Chip, 6 oz. (170g) UPC 853522000191
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1623-2022·2022-08-31
Medical device recall for temperature exposure during storage
McKesson Medical-Surgical is recalling multiple medical devices that experienced temperature excursions during storage and transport. Exposure to higher temperatures from June through August 2021 may have reduced product effectiveness.
Product
a. DERMA SCIENCES, INC. NG Strip FASTENER, NASAL TUBE IND WRAP(25/BX), Catalog NG25. b. DERMA SCIENCES, INC. Surgitube BANDAGE, GAUZE #2P 7/8"X50YDS DERSCI Catalog GL-242. c. DERMA SCIENCES, INC. Surgilast TUBE NET SZ3 MED 10YDS/EA HAND, ARM, LEG, FOOT SURGILAST…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1575-2022·2022-08-31
Baxter DISCPAC Syringe Tip Caps Recalled for Compromised Sterile Barrier
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging failure that could compromise the sterile barrier. The recall affects 602,340 units distributed worldwide.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow: a) 25 pack, REF H93866025, b) 100 pack, REF H93866100, c) 25 pack, REF H938690025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2022·2022-08-31
Mckesson Ultracell Eye Pledgets Recalled Over Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling Ultracell Eye Pledgets (Model 40825) due to temperature excursions during storage and transportation between June and August 2021 that may have compromised product effectiveness. Affected units were distributed nationwide from June through September 2021.
Product
Ultracell Eye Pledget Ultracell 2 X 6 X 1 mm, Sterile Model Number: 40825
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1564-2022·2022-08-31
Enjoy Life Soft Baked Cookies Recalled for Hard Plastic Contamination
Enjoy Life Natural Brands is recalling Soft Baked Cookies Double Chocolate Brownie due to potential hard plastic contamination. Consumers should not eat the affected product.
Product
Enjoy Life Soft Baked Cookies Double Chocolate Brownie, 6 oz (170g) UPC 853522000214
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1455-2022·2022-08-31
QP Sudfedrine PE Max Strength tablets recalled for improper storage
Family Dollar Stores is recalling QP Sudfedrine PE Max Strength tablets nationwide due to storage temperature deviations that may have compromised product quality.
Product
QP SUDFEDRINE PE MAX STRENGTH TBLT 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1570-2022·2022-08-31
FDA Recalls Exacta-Mix 2400 Compounding System for Potential Valve Leaks
Baxter Healthcare is recalling the Exacta-Mix 2400 compounding system due to potential leaking valves on ports 1-4 in certain lots. Affected units have lot numbers 60316024 and higher.
Product
The Exacta-Mix 2400 compounding system, manufactured by Baxter Healthcare Corporation, is a compounding device used in the pharmacy to compound multiple source ingredients into one final solution. This device is not intended for direct patient hook-up.
Category
Medical Device
Distribution
Distributed nationwide