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.

19176–19200 of 73543

HighFDA (Devices)·Z-1578-2022·2022-08-31
Baxter DISCPAC Syringe Tip Caps recalled due to sterile barrier failure
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps because packaging may not maintain a sterile barrier. Affected units were distributed worldwide including the US, Australia, Finland, Germany, Spain, and the UK.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF H938693025, b) 100 pack REF H938673100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1602-2022·2022-08-31
Ultrasound Probe Disinfectant Recalled: Temperature Exposure May Affect Effectiveness
Nanosonics Sonex-HL ultrasound probe disinfectant is recalled due to temperature excursions during storage that may have affected product effectiveness.
Product
NANOSONICS LTD Sonex-HL Ultrasound Probe Disinfectant trophon Sonex-HL 80 mL Bottle For Trophon EPR Disinfection System Model Number: N00037
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1384-2022·2022-08-31
Family Dollar Hydrocortisone and Cortizone Creams Recalled for Storage Deviation
Family Dollar Stores is recalling hydrocortisone cream (1 oz, SKU 910321) and Cortizone 10 Creme (0.5 oz, SKU 910167) distributed April 30 through June 10, 2022, due to improper storage temperature conditions.
Product
FS HYDROCORTISONE CREAM 1 OZ SKU 910321 CORTIZONE 10 CREME 0.5 OZ SKU 910167 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1408-2022·2022-08-31
Witch hazel product recalled for improper storage temperature conditions
Witch hazel product distributed to Family Dollar Stores from April through June 2022 was stored at improper temperatures. The FDA issued a Class II recall due to manufacturing and quality control (CGMP) deviations.
Product
TN DICKINSON WITCH HAZEL 16 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1573-2022·2022-08-31
Enjoy Life Brownie Bites recalled for potential hard plastic pieces
Enjoy Life Natural Brands is recalling Brownie Bites - Salted Caramel (4.76 oz) due to potential hard plastic pieces. Approximately 89,736 cases were distributed nationwide in the US and Canada.
Product
Enjoy Life Brownie Bites Salted Caamel, 4.76 oz UPC 819597013313
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1362-2022·2022-08-31
Divalproex Sodium Extended-Release Tablets Recalled for Failed Dissolution Specifications
Amneal Pharmaceuticals is recalling 4,309 bottles of Divalproex Sodium Extended-Release Tablets (250 mg) due to failed dissolution specifications. The tablets may not dissolve properly, potentially affecting medication effectiveness.
Product
DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1626-2022·2022-08-31
LASIK Irrigation Cannula Recalled for Potential Temperature Exposure Damage
Beaver-Visitec medical irrigation cannulas used in LASIK eye surgery are being recalled due to storage temperature excursions. Units distributed from June through September 2021 may have reduced effectiveness.
Product
BEAVER-VISITEC INTERNATIONAL, INC. Visitec CANNULA, LASIK IRR (10/BX)BVRVIS Catalog #585278
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1388-2022·2022-08-31
Arthritis Pain Reliefs Recalled for Improper Storage Temperature Conditions
Family Dollar Stores is recalling BC Arthritis Pain Fast Pain Relief and Good Sense Arthritis Caplet due to improper storage conditions. Products were distributed nationwide from April 30 through June 10, 2022.
Product
BC ARTHRITIS PAIN FAST PAIN RELIEF 24CT SKU 999839 GOOD SENSE ARTHRITIS CAPLET 24 CT SKU 914771 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1570-2022·2022-08-31
Enjoy Life Oat Breakfast Ovals Recalled for Hard Plastic Contamination
Enjoy Life Natural Brands is recalling Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals due to potential hard plastic pieces in the product. Consumers should not consume affected items.
Product
Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals Chocolate Chip Banana, 8.8 oz (250g) UPC 819597012576 and 819597012705
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1432-2022·2022-08-31
Facial Moisturizer Recalled for Improper Storage Temperature Conditions
Family Dollar Stores is recalling AMBI Nursing Daily Facial Moisturizer 1.7 oz distributed nationwide from April 30 through June 10, 2022, because the product was held outside appropriate storage temperature conditions.
Product
AMBI NRSHNG DAILY FACIAL MSTURZER 1.7 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1454-2022·2022-08-31
Multiple Cold and Flu Medications Recalled Due to Improper Storage Conditions
Family Dollar Stores is recalling multiple cold and flu medications distributed April 30–June 10, 2022, because products were held outside appropriate storage temperature conditions.
Product
DAYQUIL COLD FLU LQD 12 FL OZ SKU 900205 RIC NIGHT TIME CLD FLU RLF SOFT GELS 8 CT SKU 900523 ALKA SELTZER PLUS DAY NIGHT LGEL 20 CT SKU 902012 GS COLD FLU RELIEF NGHTTIME CHRY12FL OZ SKU 917523 RIC COLD FLU DAY TIME LIQUID CAP 16 CT SKU 903037 ASP SEVERE COLD COUGH…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1565-2022·2022-08-31
Dental Implant Recall: Nobel Biocare Device Burr Aspiration Risk
Nobel Biocare is recalling 347 N1 TiUltra TCC dental implants due to a burr that may pose an aspiration risk during surgical implantation. No injuries have been reported.
Product
Nobel Biocare N1 TiUltra TCC NP 3.5x13mm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1585-2022·2022-08-31
Medical Device Etching Solution Recalled for Potential Temperature-Related Effectiveness Loss
ABX Pentra Etching CP solution is recalled due to temperature excursions from June-August 2021 that may have affected product effectiveness. Affected lots were distributed June 1 - September 30, 2021.
Product
HORIBA ABX MEDICAL INC ABX PENTRA ETCHING CP System Fluid ABX Pentra Eching Solution CP For ABX Pentra 400 Clinical Chemistry Analyzer 25 mL. Ref: 1220001769
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1420-2022·2022-08-31
PREVACID Lansoprazole 15mg Capsules Recalled Due to Storage Conditions
Family Dollar Stores is recalling PREVACID 24HR Lansoprazole 15mg capsules distributed nationwide from April 30 to June 10, 2022, because the product was stored at improper temperatures in violation of manufacturing standards. Consumers should not use this product and should contact Family Dollar Stores for a refund.
Product
PREVACID 24HR LANSOPRAZOLE 15MG CAP 14CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1608-2022·2022-08-31
3M Grounding Safety Ring Pads Recalled Due to Temperature Exposure
3M Grounding Safety Ring pads may have been exposed to excessive temperatures during storage, potentially compromising product effectiveness. The recall affects products distributed nationwide that were received between June and September 2021.
Product
3M COMPANY 3M PAD, GROUNDING SAFETY RING Model Number: 9165
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1568-2022·2022-08-31
Enjoy Life Chewy Bars Recalled for Hard Plastic Contamination
Enjoy Life Natural Brands is recalling Chewy Bars - Caramel Blondie due to potential hard plastic pieces. About 89,736 cases were distributed in the US and Canada.
Product
Enjoy Life Chewy Bars Caramel Blondie (Chocolate Chip and Caramel), 5.75 oz (165g) UPC 819597011258 and 819597011333
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1568-2022·2022-08-31
Servo-air Ventilator Systems Lack Required Stability Warning Markings
Getinge is recalling Servo-air Ventilator Systems because they lack required warning markings about stability risks when stationary. A total of 102 units were distributed in the US; 13,750 units were distributed internationally.
Product
Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for respiratory support, monitoring and treatment of pediatric and adult patients. Model Number: 6882000 (equipped with 6881999 mobile cart)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1586-2022·2022-08-31
ABX PENTRA Creatinine Reagent Recalled Due to Temperature Excursion Exposure
Mckesson Medical-Surgical is recalling ABX PENTRA Creatinine reagent due to facility temperature excursions (June-August 2021) that may have impacted product effectiveness. Affected lots were received nationwide between June 1 and September 30, 2021.
Product
a. ABX PENTRA CREATININE 120CP JAFFE 120/130. Ref: A11A01933. b. Reagent General Chemistry Creatinine Model Number: 1220001933
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1621-2022·2022-08-31
Medical Sponges Recalled for Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling MetriSponge cleaning sponges due to facility temperature excursions that may have compromised product effectiveness during storage and delivery between June and August 2021.
Product
METREX RESEARCH CORP SPONGE, METRISPONGE W/METRIZYME (25/BX 4BX/CS) Model Number: 10-4025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2022·2022-08-31
Alere Fertility Test Pregnancy Test Kits Recalled Due to Temperature Damage
Alere Fertility Test pregnancy test kits distributed in the US have been recalled because temperature excursions during storage may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine Sample 30 Tests, Model Number: 92210. b. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere hCG Dipstick Fertility Test hCG Pregnancy Test Urine Sample 50 Tests Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1628-2022·2022-08-31
Medical Lubricating Jelly Recalled Due to Temperature Excursions During Storage
Mckesson Medical-Surgical is recalling Fisher Scientific Aseptic Control Lubricating Jelly due to temperature excursions from June–August 2021 that may have reduced product effectiveness.
Product
FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK) Catalog #22998006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1402-2022·2022-08-31
Petroleum Jelly Products Recalled for Improper Storage Conditions
Family Dollar Stores is recalling three petroleum jelly products (Swan, Baby Love, and Vaseline brands) distributed between April and June 2022 due to storage temperature deviations.
Product
SWAN PETROLEUM JELLY 7.5 OZ SKU 910721 BABY LOVE PETROLEUM JELLY 13 OZ SKU 910726 VASELINE PETROLEUM JELLY ORIGINAL 7.5 OZ 2099273 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1398-2022·2022-08-31
AZO YEAST PLUS 20 CT Recalled Due to Improper Storage Conditions
AZO YEAST PLUS 20 CT has been recalled by Family Dollar Stores due to improper storage temperature conditions that violate CGMP requirements. The product was distributed nationwide from April through June 2022.
Product
AZO YEAST PLUS 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1584-2022·2022-08-31
Surgical Hemostatic Matrix Recalled Due to Temperature Exposure During Storage
Mckesson is recalling Ethicon SURGIFLO Hemostatic Matrix Kit due to temperature excursions during storage that may have reduced product effectiveness. Affected units were distributed nationwide between June and September 2021.
Product
Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Ref: 2994 Mfg: FERROSAN MEDICAL DEVICES A/S Indicated in surgical procedures (other than ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or other conventional methods is ineffective…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2022·2022-08-31
Alcon Contact Lens Solutions Recalled for Temperature Exposure During Storage and Transit
Multiple Alcon contact lens solutions were recalled due to facility temperature excursions during storage and transit that may have reduced product effectiveness. Affected products include Clear Care and Opti Free Replenish solutions distributed nationwide between June and September 2021.
Product
a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution, Model Number: 65035820, Model Number: USSCupA-12BUP300. b. Alcon Contact Lens Solution Opti Free Replenish 4 oz. Solution Model Number: 00065035604 Model Number: USSCupA-12BUP300. c. Alcon Contact…
Category
Medical Device
Distribution
Distributed nationwide