State

Virginia product recalls

72,986 recalls have nationwide distribution and so reach Virginia. 9,483 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total: 9,483
Critical: 1,286
Severe: 2,296
Most recent: 2026-09-25

Of the 9,483 recalls naming Virginia we have scored against our rubric, 1,286 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,296 (24%) are Severe.

Which agencies issued them

These figures cover only the 9,483 recalls whose distribution notice names Virginia specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6451–6475 of 82469

SevereFDA (Drugs)·D-0499-2025·2025-07-09
Bupivacaine HCL Sterile Injection Recalled for Sterility Assurance Concerns
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Product
BUPIVAcaine HCL Sterile injection, USP w/EPINEPHRINE 1:200,000, 50 mg/10mL, 0.5%, (5mg/mL), 10 mL Sterile Single-Dose Vial, Rx Only, For Nerve Block, Caudal & Epidural Anesthesia Only, Warning: Contains Sulfites, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0146-2025·2025-07-09
Zenshi crunchy tuna roll trays made with recalled cucumbers
Zenshi Handcrafted Sushi Crunchy Roll with tuna is being recalled over cucumbers recalled for possible Salmonella. 4,005 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Tuna 10pc Net Wt 10.0oz UPC 0 23012 95041 5
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0153-2025·2025-07-09
Zenshi crunchy California and rainbow duo combo used recalled cucumbers
Zenshi Handcrafted Sushi Duo Combo with Crunchy California and Rainbow Roll is being recalled over cucumbers recalled for possible Salmonella. 5,238 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Duo Combo - Crunchy CA & Rainbow Roll 10pc Net Wt 8.6oz UPC 0 23012 94206 9
Category
Food
Distribution
8 states
SevereFDA (Drugs)·D-0569-2025·2025-07-09
Sandoz cefazolin cartons contained vials labeled as penicillin G potassium
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Product
CEFAZOLIN — CEFAZOLIN (CEFAZOLIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0505-2025·2025-07-09
Zicam Nasal AllClear swabs recalled over fungal contamination of swabs
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.
Product
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0124-2025·2025-07-09
Zenshi California salad brown rice rolls made with recalled cucumbers
Zenshi Handcrafted Sushi California Salad Roll on brown rice is being recalled over cucumbers recalled for possible Salmonella. 240 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI California Salad Roll 10pc (Brown Rice) Net Wt. 7.1oz (201g) UPC 0 23012 94267 & 0 UPC 0 23012 95139 9
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0150-2025·2025-07-09
Zenshi sushi duo combo trays made with Salmonella-recalled cucumbers
Zenshi Handcrafted Sushi Duo Combo trays are being recalled because they were made with cucumbers recalled over possible Salmonella. 217 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Duo Combo - CA Salad & Rainbow Roll 10pc Net Wt 8.1oz UPC 0 23012 94205 2
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0136-2025·2025-07-09
Zenshi salmon cream cheese roll trays used recalled cucumbers
Zenshi Handcrafted Sushi Cream Cheese Roll with salmon is being recalled over cucumbers recalled for possible Salmonella. 5,350 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Cream Cheese Roll - Salmon 10pc Net Wt 7.1oz UPC 0 23012 94275 5
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0122-2025·2025-07-09
Zenshi California roll trays made with recalled cucumbers
Zenshi Handcrafted Sushi California Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 39,743 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI California Roll 10pc Net Wt. 7.1oz (201g) UPC 0 23012 94264 9, UPC 023012 95138 2 & UPC 0 23012 90618 4
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0172-2025·2025-07-09
Zenshi hybrid Ni sushi platters made with recalled cucumbers
Zenshi Handcrafted Sushi Hybrid Ni Platter is being recalled because it was made with cucumbers recalled over possible Salmonella. 7 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Hybrid Ni Platter 31pc Net Wt. 33.1oz UPC 0 23012 94258 8
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0165-2025·2025-07-09
Zenshi Hawaiian roll sushi trays made with recalled cucumbers
Zenshi Handcrafted Sushi Hawaiian Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 1,269 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Hawaiian Roll 10pc Net Wt. 11.0oz UPC 0 23012 94363 9
Category
Food
Distribution
8 states
SevereFDA (Food)·H-0163-2025·2025-07-09
Zenshi happy heart rainbow red rock platters used recalled cucumbers
Zenshi Handcrafted Sushi Happy Heart Platter #2 is being recalled over cucumbers recalled for possible Salmonella. 2,609 trays are affected.
Product
ZENSHI HANDCRAFTED SUSHI Happy Heart Platter #2 (Rainbow Red Rock) 13pc Net Wt. 14.9oz UPC 0 23012 94483 4
Category
Food
Distribution
8 states
SevereFDA (Devices)·Z-2037-2025·2025-07-09
BiPAP A40 ventilators are not indicated for respiratory failure patients
The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.
Product
BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2013-2025·2025-07-09
Servo-u ventilators may measure patient circuit compliance inaccurately
The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.
Product
Servo-u Ventilator System. Model Number: 6688600.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2035-2025·2025-07-09
BiPAP V30 Auto ventilators are not indicated for respiratory failure
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Product
BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2048-2025·2025-07-09
Philips Ultrasound Transducers Recalled After Over-Refurbishment
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Product
Philips 3D9-3v Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2043-2025·2025-07-09
Medline IV Catheters Recalled for Needle Retraction Failure
Medline Industries is recalling specific Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters because the needle may be slow to retract or fail to retract during catheter insertion.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, REF ACC010256; 3) PEDI EMERGENCY TRAY-BLUE, REF ACC010316A; 4) ADULT DRAWER 4, REF ACC010389C;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0500-2025·2025-07-09
Compounded ketamine injection recalled over lack of sterility assurance concerns
Ketamine Hydrochloride Injection compounded by Medivant Healthcare is being recalled for lack of assurance of sterility after an FDA inspection raised concerns about the sterile manufacturing process.
Product
KETAmine Hydrochloride Injection, USP, 50 mg/5mL (10 mg/mL), For IM Use or Slow IV Use, 5 mL Sterile Single-Dose Vial, Rx Only, For Office Use Only, Compounded Durg by: Medivant Healthcare, 158 S. Kyrene Rd. Chandler, AZ 85226, NDC 81483-0006-0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0144-2025·2025-07-09
Harris Teeter Sushi Rolls Recalled Over Salmonella Risk
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Salmon products due to possible Salmonella contamination from recalled cucumbers used in production.
Product
ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Salmon 10pc Net Wt. 10.0oz UPC 0 23012 95040 8
Category
Food
Distribution
8 states
HighFDA (Food)·H-0130-2025·2025-07-09
Harris Teeter Sushi Recall Over Possible Salmonella Contamination
Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI Chef Sampler B#2 (Dragon Salmon Cheese) due to possible Salmonella contamination from recalled cucumbers used in the sushi.
Product
ZENSHI HANDCRAFTED SUSHI Chef Sampler B#2 (Dragon Salmon Cheese) 15pc Net Wt. 11.9oz (337g) UPC 0 23012 94338 7
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-2040-2025·2025-07-09
VITROS 4600 chemistry systems may report results using expired diluent packs
VITROS 4600 Chemistry Systems are being recalled because a software anomaly can allow results to be reported using diluent packs the system treats as expired, which can produce erroneous results.
Product
Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software Version: version 3.2 to version 3.8.3 (all available software versions) Product Description: In vitro diagnostic chemistry analyzer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0203-2025·2025-07-09
Peak Cocktails blood orange spritz cans may overpressurize and explode
Peak Cocktails Blood Orange Spritz in 8.4 fl oz cans is being recalled because of overpressurization leading to exploding cans. 16,128 units are affected.
Product
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24, and 48 cans. Batch Codes: B25127, B25128; Packaging Date: 05/07/2025, 05/08/2025
Category
Food
Distribution
50 states
HighFDA (Devices)·Z-2045-2025·2025-07-09
Medline retinal packs recalled because catheter needle may fail to retract
Medline RETINAL PACK-LF convenience kits are being recalled because the BD Insyte Autoguard catheter needle inside may be slow to retract or fail to retract during insertion. 80 units affected.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: RETINAL PACK-LF, REF DYNJ0151148B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2058-2025·2025-07-09
Philips S5-1 Ultrasound Transducers Refurbished Beyond Useful Life
Philips Ultrasound is recalling Philips S5-1 Transducers because they were refurbished beyond their useful life, which may affect device performance and safety.
Product
Philips S5-1 Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2025·2025-07-09
Bard Urologist's Tray Recalled Over Incorrect French Size Labeling
C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.
Product
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Category
Medical Device
Distribution
Distributed nationwide