State

Virginia product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6826–6850 of 82475

SevereFDA (Food)·H-0010-2025·2025-06-11
Albertsons Greek Salad Products Recalled for Salmonella Contamination
Albertsons Companies LLC is recalling three Greek salad products due to Salmonella contamination from recalled cucumbers supplied by Bedner Grower's Company. The contaminated salads are linked to an ongoing outbreak.
Product
AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 293070 ##### READY MEALS GREEK SALAD SS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 292483 ##### Star Market GREEK SALAD FS, Refrigerated, packaged i
Category
Food
Distribution
13 states
SevereFDA (Drugs)·D-0456-2025·2025-06-11
Fluoxetine Tablets 20 mg Recalled for N-Nitroso Impurity
Torrent Pharma Inc. is recalling Fluoxetine Tablets, USP, 20 mg in a 28-count carton due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit.
Product
FLUOXETINE — FLUOXETINE (FLUOXETINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0004-2025·2025-06-11
Ukrop's Marinated Cucumber Salad Recalled for Salmonella Contamination
Ukrop's Marinated Cucumber Salad is recalled due to Salmonella contamination from cucumbers supplied by Bedner Farms. The product was distributed to Kentucky, North Carolina, Ohio, Virginia, and West Virginia.
Product
Ukrop's Marinated Cucumber Salad INGREDIENTS: Cucumber, distilled vinegar***apple cider vinegar, sugar, red onion, water, canola oil***NET WT 16 OZ (1LB/454g) UPC 7 22515 24902 5; NET WT 36 OZ (2.25LB/1.02kg) UPC 7 22515 25224 7; NET WT 5LB (2.27kg) UPC 7 22515 29354 7 Ukrop's Ho
Category
Food
Distribution
5 states
HighNHTSA·25V387000·2025-06-11
Rivian R1S and R1T front turn signals may fail to illuminate
Rivian is recalling certain 2025 R1S and R1T vehicles because one or both front turn signals may fail to illuminate and flash, failing FMVSS 108. 27,882 units affected.
Product
RIVIAN — RIVIAN R1S, R1T
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1908-2025·2025-06-11
Beckman Coulter Sample Probes with Defective Tips Clinical Chemistry
Beckman Coulter is recalling sample probes with defective tips used in clinical chemistry analyzers. The defective probes may dispense lower sample concentrations, potentially leading to false low test results and delayed diagnosis.
Product
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1888-2025·2025-06-11
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack recalled
Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.
Product
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1895-2025·2025-06-11
Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect
Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.
Product
Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1887-2025·2025-06-11
Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall
Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.
Product
Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0928-2025·2025-06-11
GNC Women's 30+ Vitapak recalled due to undeclared fish allergen
GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.
Product
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-1899-2025·2025-06-11
Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall
Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.
Product
Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0011-2025·2025-06-11
Giant Instant Oatmeal Raisins and Spice Recalled for Undeclared Walnuts
Giant Instant Oatmeal Raisins and Spice is being recalled because walnuts are not declared on the outer packaging, though they appear on the inner packaging. Consumers with walnut allergies who rely on outer-package labeling are at risk.
Product
Giant, Instant Oatmeal Raisins and Spice, 10 -1.5 oz. Packets, per box. Net. Wt. 15.01 oz.
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-1893-2025·2025-06-11
Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect
Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.
Product
Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2025·2025-06-11
Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled
Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.
Product
Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1896-2025·2025-06-11
Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall
Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.
Product
Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1911-2025·2025-06-11
Olympus EVIS EXERA III Duodenovideoscope TJF-Q190V Contamination Risk
Olympus is recalling the EVIS EXERA III Duodenovideoscope Model TJF-Q190V due to post-market data showing higher microbial contamination when manual cleaning is delayed beyond one hour after patient use.
Product
Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1885-2025·2025-06-11
Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled
Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.
Product
Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0008-2025·2025-06-11
Bengal King Family Pack Vegetable Singara Contains Undeclared Peanut
South Asian Food Inc. is recalling Bengal King Family Pack Vegetable Singara due to undeclared peanut, a major allergen that poses a serious risk to consumers with peanut allergies.
Product
Bengal King Family Pack Vegetable Singara
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1903-2025·2025-06-11
Luminex VERIGENE Gram Negative Blood Culture Test Recalled
Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.
Product
VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1889-2025·2025-06-11
MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect
Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.
Product
MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1900-2025·2025-06-11
Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall
Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.
Product
Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1910-2025·2025-06-11
ChannelCheck Convenience Pack Pre-filled Water Syringes Recalled
Healthmark Industries is recalling ChannelCheck Convenience Pack Pre-filled Water Syringes (Models UCC-222CP and UCC-222-ESP) because contamination was found in duodenoscope samples linked to the syringes, which were improperly used outside their intended purpose.
Product
ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1894-2025·2025-06-11
Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled
Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.
Product
Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1898-2025·2025-06-11
Signature Laparoscopic Alligator Grasper Instrument Recall Safety Issue
Silex Medical is recalling the Signature Laparoscopic Alligator Grasper with Rotating Shaft (Model 5863050) because insulation on the tube does not fully extend to the proximal end of the shaft, leaving an exposed uninsulated area near the rotator wheel.
Product
Signature Laparoscopic Instruments, Alligator Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863050.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V365000·2025-06-11
Mercedes-Benz Recalls 2023 GLC 300 Models for Missing Headlight Caps
Mercedes-Benz is recalling 2023 GLC 300 and GLC 300 4MATIC vehicles because missing caps allow improper headlight adjustment, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLC 300, GLC 300 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0455-2025·2025-06-11
Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination
Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.
Product
FLUOXETINE — FLUOXETINE (FLUOXETINE)
Category
Drug
Distribution
Distributed nationwide