The Recall Desk

State

Virginia product recalls

72,940 recalls have nationwide distribution and so reach Virginia. 9,479 additional recalls listed Virginia specifically in their distribution scope.

What the numbers show

Total
9,479
Critical
1,285
Severe
2,294
Most recent
2026-09-09

Of the 9,479 recalls naming Virginia we have scored against our rubric, 1,285 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,294 (24%) are Severe.

These figures cover only the 9,479 recalls whose distribution notice names Virginia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4901–4925 of 82419

  • CriticalFDA (Food)·H-0088-2026·2025-10-29

    Deli pasta salad recalled because it may contain Listeria monocytogenes

    Sprouts Farmers Market is recalling Smoked Mozzarella Pasta Salad sold at deli counters and in grab-and-go containers because the product may contain Listeria monocytogenes.

    Product
    Sprouts Smoked Mozzarella Pasta Salad, RTE Pasta Salad, Refrigerated, 5 day shelf life, packaged into plastic containers at Deli counter and into 16oz plastic grab & go containers, weight dependent on customer request, UPC 2-15587-00000 (from service case) and 2-15786-00000 (from
    Category
    Food
    Distribution
    24 states
  • SevereNHTSA·25V737000·2025-10-29

    Mazda CX-50 front suspension bolts may allow wheel detachment

    Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.

    Product
    MAZDA — MAZDA CX-50, CX-50 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0035-2026·2025-10-29

    Alcohol prep pads recalled from one lot as a subpotent drug

    Medline is recalling 222,800 alcohol prep pads from one lot because the product is subpotent.

    Product
    Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0112-2026·2025-10-29

    Frozen cooked shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0232-2026·2025-10-29

    Insulin pumps recalled over software defect causing unexpected correction bolus

    Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.

    Product
    t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0207-2026·2025-10-29

    PVC stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0208-2026·2025-10-29

    Silicone stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0211-2026·2025-10-29

    Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0209-2026·2025-10-29

    Gastric sump anti-reflux valves recalled after breakage complaints from excessive force

    Cardinal Health is recalling all lots of Salem Sump Anti-Reflux Valves after complaints of valve breakage due to excessive force during use, and is providing additional guidance for use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2026·2025-10-29

    Automated microbiology systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0238-2026·2025-10-29

    BD MAX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0288-2026·2025-10-29

    Defibrillator pad packs recalled over damaged pins disrupting electrical contact

    HeartSine Technologies is recalling 1,291,165 Pad-Pak units because defibrillator pads may contain damaged pins that disrupt the mechanical fit and electrical contact.

    Product
    HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0234-2026·2025-10-29

    Prefilled saline flush syringes recalled over sodium chloride concentration shortfall

    Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.

    Product
    Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0114-2026·2025-10-29

    Frozen cooked salad shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0235-2026·2025-10-29

    Microbiology data systems recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUTER OPTIPLEX EPICENTER SPARE, Catalog Number: 441421. 3. Generic NUC 2, Catalog Number: 445398. 4. Nuc 5i5 Os Image Bow 2.X, C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0116-2026·2025-10-29

    Frozen shrimp skewers recalled in expanded cesium 137 contamination action

    Southwind Foods is recalling Great American branded frozen raw shrimp skewers made under insanitary conditions in which the product may have been contaminated with Cesium-137.

    Product
    Great American branded Frozen raw shrimp skewer; 1lb bag UPC: 829944002716; 829944002372
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0233-2026·2025-10-29

    Oral thermometer probes recalled after being programmed with rectal configuration

    Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.

    Product
    Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0236-2026·2025-10-29

    BACTEC FX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 177 BD BACTEC Blood Culture System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BD BACTEC FX, Instrument Top, Packaged, Catalog Number: 44138509. 2. Instrument Top Remanufactured Bactec Fx, Catalog Number: 441676. 3. BACTEC 9240 System, Catalog Number: 445569. 4. BD BACTEC FX40 Instrum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0036-2026·2025-10-29

    Ketorolac injection vials recalled after glass particulate found in product

    Aspiro Pharma is recalling Ketorolac Tromethamine Injection USP 60 mg/2 mL across several lots because of particulate matter identified as glass.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0115-2026·2025-10-29

    Tovala frozen raw shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Tovala branded frozen raw phosphate free shrimp in 5 oz bags because it may have been contaminated with Cesium-137.

    Product
    Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0237-2026·2025-10-29

    Blood culture systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
    Category
    Medical Device
    Distribution
    Distributed nationwide