State

US Virgin Islands product recalls

73,213 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 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16026–16050 of 73390

HighFDA (Drugs)·D-0622-2023·2023-05-24
Piperacillin and Tazobactam Injectable Recalled for Sterility Assurance Issue
Astral SteriTech is recalling 204,860 vials of Piperacillin and Tazobactam for Injection due to lack of assurance of sterility. The FDA classified this as a Class II recall affecting nationwide distribution.
Product
Piperacillin and Tazobactam for Injection, USP, 4.5 grams per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-577-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0582-2023·2023-05-24
Ampicillin Injection Vials Recalled for Sterility Assurance Failure
Astral SteriTech is recalling approximately 89,690 vials of Ampicillin for Injection due to lack of assurance of sterility. The product was distributed nationwide.
Product
Ampicillin for Injection, USP 1g per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-222-41
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1603-2023·2023-05-24
Immundiagnostik Lactoferrin ELISA Kit Recalled for Lacking FDA 510(k) Clearance
IMMUNDIAGNOSTIK Inc. has recalled the IDK Lactoferrin ELISA diagnostic kit because it was marketed without the required FDA 510(k) premarket notification. No illnesses or injuries have been reported.
Product
Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended for the determination of lactoferrin in stool. P/N: K6870 Single Kit P/N: K6870.20.US.L 20 Plates
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0629-2023·2023-05-24
Piperacillin and Tazobactam for Injection Recalled for Lack of Sterility Assurance
The FDA is recalling 169,520 vials of Piperacillin and Tazobactam injectable antibiotic due to lack of assurance of sterility. The affected vials were distributed nationwide.
Product
Piperacillin and Tazobactam for Injection, USP 2.25 g per vial,s Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-078-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0592-2023·2023-05-24
Ampicillin-Sulbactam Injection Recalled Due to Sterility Concerns
FDA recalls Ampicillin and Sulbactam for Injection (1.5 grams per vial) manufactured by Astral SteriTech due to lack of sterility assurance. The recall affects 236,610 vials distributed nationwide.
Product
Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-005-20
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1580-2023·2023-05-24
Breathing circuit swivel elbow recalled for inadequate sterilization instructions
Smiths Medical is recalling DuraLife Swivel Elbow breathing circuit devices due to inadequate sterilization instructions. The device instructions lack cleaning methods, autoclave cycle duration, and reuse specifications.
Product
DuraLife Autoclavable Double Swivel Elbow, REF 60-0010 (UltraSet Product Code 66-1991); Swivel Elbow with Suction Port for use with breathing circuits
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0630-2023·2023-05-24
Piperacillin and Tazobactam Injection Recalled Due to Sterility Assurance Issue
Approximately 936,680 vials of Piperacillin and Tazobactam for Injection are being recalled nationwide due to lack of assurance of sterility. All affected lots remain within their expiration dates.
Product
Piperacillin and Tazobactam for Injection, UPS, 3.375 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-079-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0625-2023·2023-05-24
Piperacillin and Tazobactam Injection Recalled for Sterility Assurance Failure
Meitheal Pharmaceuticals is recalling Piperacillin and Tazobactam for Injection due to lack of sterility assurance. The recalled product may pose an infection risk to patients if used.
Product
Piperacillin and Tazobactam for Injection, USP 4.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-004-51
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0579-2023·2023-05-24
Heparin Sodium and Dextrose Injection Recalled Due to Subpotency
B. Braun Medical Inc. is recalling 1,380 units of Heparin Sodium in Dextrose injection because the product is subpotent with lower anti-factor IIa potency than specified.
Product
HEPARIN SODIUM IN DEXTROSE — HEPARIN SODIUM IN DEXTROSE (HEPARIN SODIUM AND DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0601-2023·2023-05-24
Ampicillin and Sulbactam Injectable Recalled for Sterility Assurance Defect
The FDA has recalled Ampicillin and Sulbactam for Injection due to lack of assured sterility. Approximately 119,340 vials distributed nationwide within the United States are affected.
Product
Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-081-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0580-2023·2023-05-24
Ampicillin for Injection Recall Due to Sterility Assurance Concerns
Astral SteriTech is recalling 70,040 vials of Ampicillin for Injection nationwide due to lack of assurance of sterility in the manufacturing process.
Product
Ampicillin for Injection, USP 250 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-220-41
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0627-2023·2023-05-24
Piperacillin and Tazobactam Injection Recalled for Lack of Sterility Assurance
Astral SteriTech recalls 223,590 vials of Piperacillin and Tazobactam for Injection nationwide due to lack of assured sterility. Patients and healthcare providers should stop use and consult their provider.
Product
Piperacillin and Tazobactam for Injection, USP, 3.375 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-217-41
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1585-2023·2023-05-24
Philips Incisive CT system foot switch poses entrapment risk during unload
The Philips Incisive CT system's foot switch may trap the operator's foot during the unload function, causing injury. The FDA has issued a Class II recall affecting 46 units worldwide.
Product
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0619-2023·2023-05-24
Injectable Ceftriaxone Recalled for Lack of Sterility Assurance
Astral SteriTech is recalling 243,825 vials of Ceftriaxone for Injection due to inability to assure sterility. The medication was distributed nationwide and poses a contamination risk.
Product
Ceftriaxone for Injection, USP, 2 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-097-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0616-2023·2023-05-24
Ceftriaxone Injectable Antibiotic Recalled Nationwide for Sterility Assurance Deficiency
Astral SteriTech's 66,125-vial ceftriaxone injection is being recalled nationwide due to lack of assurance of sterility in manufacturing. The product is distributed across the United States.
Product
Ceftriaxone for Injection, USP 250 mg per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-094-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0624-2023·2023-05-24
Piperacillin and Tazobactam for Injection Recalled Due to Sterility Assurance Failure
Astral SteriTech recalls approximately 893,950 vials of piperacillin and tazobactam injection nationwide because the manufacturer cannot assure the product was properly sterilized.
Product
Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-003-31
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0611-2023·2023-05-24
Ceftriaxone injection vials recalled for lack of sterility assurance
Astral SteriTech is recalling approximately 66,250 vials of Ceftriaxone for Injection due to lack of sterility assurance. The injectable antibiotic poses a potential contamination risk if used.
Product
Ceftriaxone for Injection, USP 250 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-211-42
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0596-2023·2023-05-24
Ampicillin and Sulbactam for Injection Recalled Due to Sterility Concerns
Ampicillin and Sulbactam for Injection is being recalled nationwide due to lack of assurance of sterility. Approximately 58,770 vials manufactured by Astral SteriTech Private Ltd. are affected.
Product
Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-241-41
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1581-2023·2023-05-24
DuraLife Breathing Circuit Extension Tube Recall Due to Inadequate Sterilization Instructions
Smiths Medical is recalling 2,101 DuraLife Autoclavable Silicone Extension Tubes due to inadequate sterilization instructions. The product documentation does not specify cleaning methods, autoclave cycle duration, or the number of reuse cycles allowed per patient.
Product
DuraLife Autoclavable Silicone Extension Tube, REF 60-1502 (UltraSet Product Code 66-2509); Non-Ported Double Swivel Elbow for use with breathing circuits
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0606-2023·2023-05-24
Cefepime for Injection Recalled Due to Sterility Assurance Concerns
The FDA is recalling Cefepime for Injection 2 grams per vial due to inability to assure product sterility. No illnesses have been reported.
Product
Cefepime for Injection, USP 2 grams per vial, Rx only, Mfd. for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-009-20
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0589-2023·2023-05-24
Ampicillin Injection Recalled for Lack of Sterility Assurance
Astral SteriTech has recalled approximately 7,214 bottles of Ampicillin for Injection due to lack of assurance of sterility. The product was distributed nationwide within the United States.
Product
Ampicillin for Injection, USP 10 grams per Pharmacy Bulk Package, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-088-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0621-2023·2023-05-24
Piperacillin and Tazobactam for Injection Recalled for Lack of Sterility Assurance
Astral SteriTech is recalling approximately 1.3 million vials of Piperacillin and Tazobactam for Injection nationwide due to lack of assurance of sterility during manufacturing.
Product
Piperacillin and Tazobactam for Injection, USP, 3.375 grams per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-576-10
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V365000·2023-05-24
Loose Seat Belt Attachment in Winnebago and Itasca Motorhomes
Winnebago and Itasca recall certain 2020-2023 motorhomes due to improperly tightened seat belt attachments that may fail to restrain occupants in a crash. Dealers will tighten fasteners free of charge.
Product
WINNEBAGO — WINNEBAGO, ITASCA INSPIRE, ADVENTURER, VISTA, SHELL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1586-2023·2023-05-24
Philips Incisive CT System Foot Switch Pedal May Cause Foot Entrapment Injury
Philips Incisive CT System foot switch unload pedal may trap an operator's foot, causing injury. The FDA is recalling 5 units (3 in the US, 2 internationally) with this entrapment hazard.
Product
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0587-2023·2023-05-24
Ampicillin for Injection Recalled Due to Sterility Assurance Defect
Astral SteriTech Private Ltd. is recalling Ampicillin for Injection due to manufacturing controls that cannot assure product sterility. The FDA Class II recall affects approximately 80,850 vials distributed nationwide.
Product
Ampicillin for Injection, USP 1g per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-086-02
Category
Drug
Distribution
Distributed nationwide