The Recall Desk

State

Virginia product recalls

20,188 recalls have nationwide distribution and so reach Virginia. 0 additional recalls listed Virginia specifically in their distribution scope.

About recalls in Virginia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Virginia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

8076–8100 of 20188

  • SevereFDA (Food)·F-1661-2024·2024-08-14

    Sunny Select Strawberry Yogurt Coated Pretzels Recalled for Salmonella Risk

    Palmer & Company is recalling Sunny Select Strawberry Yogurt Coated Pretzels (10 oz, UPC 9848796055) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Sunny Select Strawberry Yogurt Coated Pretzels, Net Wt. 10 oz, UPC 9848796055, 12/10oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1665-2024·2024-08-14

    Palmer Candy Munchy Medley products recalled due to potential salmonella contamination

    Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.

    Product
    1. Palmer Candy Munchy Medley, Item 38004, Net Wt. 16/6oz bulk case, UPC 77232 38004 2. Palmer Candy Munch Medley, Item 10737, Net Wt. 15 lbs, UPC 77232 10737 3. Casey's Munchy Medley, Sweet & Salty Crunch Mix, Net Wt. 4.25 oz, UPC 98437 26083 6/case 4. Snackin' with the Crew! Mi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1672-2024·2024-08-14

    Palmer Patriotic Pretzels recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Patriotic Pretzels due to potential salmonella contamination. The affected products were distributed nationwide in the United States and Canada.

    Product
    1. Palmer Patriotic Pretzels, White & Chocolatey Fudge Covered Star Shaped Pretzels, Net Wt. 6oz, UPC 77232 37055, 16/6oz case 2. Palmer Patriotic Pretzels, White & Chocolatey Fudge Covered Star Shaped Pretzels, Net Wt 14 oz, UPC 7723237059, 12/14 oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1667-2024·2024-08-14

    Palmer Candy Chow Down Mix Recalled Due to Potential Salmonella

    Palmer & Company is recalling Palmer Candy Chow Down Mix (Item 10731, 25 lbs, UPC 77232 10731) distributed nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Palmer Candy Chow Down Mix, Item 10731, Net Wt 25lbs, UPC 77232 10731
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1658-2024·2024-08-14

    Urge! and Casey's Caramel Pretzels Recalled for Potential Salmonella

    Palmer & Company is recalling Urge! Caramel Swirl Pretzels and Casey's Caramel Swirl Coated Pretzels nationwide due to potential Salmonella contamination.

    Product
    1. Urge! Caramel Swirl Pretzels, White Fudge Coated Pretzel Twists Drizzled in Caramel, Net Wt. 6oz, UPC 39779 00417, 8/6oz case 2. Casey's Caramel Swirl Coated Pretzels, Net Wt. 4 oz., UPC 98437 26082, 6/4oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1662-2024·2024-08-14

    Palmer Candy Pretzel Rods recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Candy Vanilla Chocolatey Swirl Enrobed Pretzel Rods (8 oz) nationwide due to potential Salmonella contamination. Consumers should not consume this product.

    Product
    Palmer Candy Vanilla Chocolatey Swirl Enrobed Pretzel Rods, Crunchy Salted Pretzel Coated with White Fudge and a Fancy Chocolatey Swirl, Net Wt. 8oz, UPC 77232 17011, 12/8oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1655-2024·2024-08-14

    Palmer Zebra Fudge Cookies recalled for potential salmonella contamination

    Palmer & Company is recalling Palmer Zebra Fudge Cookies due to potential salmonella contamination. The product was distributed nationwide in the United States and Canada.

    Product
    1. Palmer Zebra Fudge Cookies, Enrobed Chocolatey Sandwich Cookies, Net Wt. 7 oz, UPC 77232 37064, distributed in case labeled Chocolate & Frosted Cookies, 16/7oz tubs/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1668-2024·2024-08-14

    Palmer Frosted Munchy Medley Snack Mix Recalled for Salmonella

    Palmer & Company is recalling Palmer Frosted Munchy Medley snack mix nationwide (US and Canada) due to potential salmonella contamination. Consumers should not eat the product and should discard it or return it to where purchased.

    Product
    Palmer Frosted Munchy Medley, A mixture of Sweet & Salty Favorites, Net Wt 15 oz., UPC 77232 37013, 8/15oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1660-2024·2024-08-14

    Patriotic Pretzel Products Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists and Palmer Candy Frosted Patriotic Pretzels nationwide due to potential salmonella contamination.

    Product
    1. Freshness Guaranteed Patriotic Red, White & Blue Pretzel Twists, Net Wt 14 oz., UPC 78742 03913, 8/14oz case 2. Palmer Candy Frosted Patriotic Pretzels, Item 10757, Net Wt 28 lbs, UPC 77232 10757
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1659-2024·2024-08-14

    Palmer Candy Cookies & Cream Yummy Chow Recalled for Salmonella Contamination Risk

    Palmer & Company is recalling Palmer Candy Cookies & Cream Yummy Chow (Item 10706) nationwide due to potential salmonella contamination. Consumers should not consume the product.

    Product
    Palmer Candy Cookies & Cream Yummy Chow, Item 10706, Net Wt. 14 lbs, UPC 77232 10706
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1670-2024·2024-08-14

    Peanut Butter Snack Mix Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Freshness Guaranteed Peanut Butter Snack Mix due to potential salmonella contamination. The recall affects 12oz and 4.5oz packages distributed nationwide in the United States and Canada.

    Product
    1. Freshness Guaranteed Peanut Butter Snack Mix, Net Wt 12oz, UPC 78742 03912, 8/12oz case 2. Peanut Butter Snack Mix, Net Wt 4.5oz to go container, Distributed by: Kwik Trip Inc; UPC 39779 00424, 12/4.5oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1666-2024·2024-08-14

    FDA Recalls Tiger Treats for Potential Salmonella Contamination

    Palmer & Company is recalling Snackin' With The Crew! Tiger Treats for potential salmonella contamination. The recalled products have best-by dates of 12/18/24 and 12/19/24 and were distributed nationwide in the U.S. and Canada.

    Product
    Snackin' With The Crew! Tiger Treats, Net Wt 8oz., UPC 7723222301, 16/8oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0626-2024·2024-08-14

    Dietary supplement tainted with undeclared pharmaceuticals recalled nationwide

    Umary Acido Hialuronico dietary supplement (850 mg caplets) was recalled nationwide by the FDA for containing undeclared Diclofenac and Omeprazole. The product was marketed without an approved drug application.

    Product
    Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0631-2024·2024-08-14

    Acetaminophen tablets incorrectly labeled with aspirin drug facts information

    Some bottles of Acetaminophen Extra Strength 500 mg tablets are labeled with the drug facts information for Aspirin 81 mg tablets. The affected lot is 4138197 (expiration 10/31/2025), distributed nationwide.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2541-2024·2024-08-14

    Everest Bipolar Cutting Forceps Recalled for Potential Sterility Breach

    Olympus is recalling Everest Bipolar Cutting Forceps due to fractures and breakages in packaging trays and Tyvek covers that may result in a sterility breach. Approximately 6985 units are affected and were distributed worldwide.

    Product
    The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forceps. Coagulation is achieved using electrosurgical energy under visualization. The device is to be used with bipolar outputs of c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2542-2024·2024-08-14

    Olympus Everest Bipolar Cutting Forceps Recalled for Packaging Defects

    Olympus is recalling Everest Bipolar Cutting Forceps due to fractures and breakages in packaging trays and Tyvek covers that may compromise sterility. The recall affects 4,364 units distributed worldwide.

    Product
    The Everest Bipolar Cutting Forceps are intended to be passed through a 5-mm or 10-mm cannula, depending on the model/outer diameter size of the forceps. Coagulation is achieved using electrosurgical energy under visualization. The device is to be used with bipolar outputs of c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2525-2024·2024-08-14

    Siemens x-ray display system support arm may lower unexpectedly

    Siemens Luminos Agile Max x-ray imaging systems have a support arm that may unintentionally lower during display positioning, creating an injury risk.

    Product
    Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2510-2024·2024-08-14

    Philips IntelliVue Patient Monitors lack critical software monitoring options

    Philips IntelliVue Patient Monitors (models MX400/450/500/550) with software versions L.x or M.x are missing three monitoring capability options (MOS, M06, M20) due to software changes, creating potential for delayed or incorrect treatment. The recall involves 18 units distributed nationwide and internationally.

    Product
    IntelliVue Patient Monitor MX500 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866064. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2487-2024·2024-08-14

    BD PYXIS medication cabinet software error causes incorrect bin labels

    A software issue in the BD PYXIS MDBNK medication dispensing cabinet may cause restock labels to print with incorrect bin locations, potentially affecting medication storage accuracy.

    Product
    BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2500-2024·2024-08-14

    BD PYXIS MEDBANK Software Issue Causes Incorrect Medication Bin Labels

    A software issue in BD PYXIS MEDBANK automated dispensing cabinets can cause incorrect medication bin labels to print during restocking. This could lead to medication dispensing errors in healthcare facilities.

    Product
    BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2517-2024·2024-08-14

    American Contract Systems Hand Pack Convenience Kit Sterilization Failure

    American Contract Systems is recalling Hand Pack convenience kits that may not be sterile due to insufficient aeration time during sterilization. Affected devices distributed in CA, KS, ME, MN, MO, NE, and SD may pose a safety risk.

    Product
    American Contract Systems Hand Pack convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1657-2024·2024-08-14

    Palmer Patriotic Snack Mix Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Palmer Patriotic Snack Mix (13 oz, Best By 1/19/25–2/1/25) due to potential Salmonella contamination. The product was distributed nationwide in the United States and Canada.

    Product
    Palmer Patriotic Snack Mix, A Seasonal Mix of Sweet & Salty Favorites, Net Wt. 13 oz., UPC 77232 37061, 12/13oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2520-2024·2024-08-14

    Medical Procedure Kit Recalled Over Potential Sterilization Compromise

    American Contract Systems is recalling Special Procedure Pack convenience kits due to insufficient aeration time during sterilization, which may have compromised sterility. Distributed in California, Kansas, Maine, Minnesota, Missouri, Nebraska, and South Dakota.

    Product
    American Contract Systems Special Procedure Pack convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2493-2024·2024-08-14

    Medication dispensing cabinet software issue causes incorrect medication bin labels

    A software issue in BD PYXIS MEDBANK automated medication dispensing cabinets can cause incorrect medication bin labels on restock labels, potentially leading to medication storage errors.

    Product
    BD PYXIS MEDBANK TWR MN CR-2HH-6FH, REF: 169-88 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2539-2024·2024-08-14

    Medical Device Hookup Instructions Contain Errors Affecting Endoscope Disinfection

    Steris Corporation recalls certain automated endoscope reprocessor hookups due to incorrect instructions in product documentation. Improper hookup connection could prevent proper endoscope disinfection, risking patient infection.

    Product
    Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups provide the interface between DSD Automated Endoscope Reprocessors ( AER ) and endoscopes, which allow perfusion of liquids dispensed by the AER to contact and high-level disinfect the channels of flexib
    Category
    Medical Device
    Distribution
    Distributed nationwide