The Recall Desk

State

Wyoming product recalls

20,189 recalls have nationwide distribution and so reach Wyoming. 0 additional recalls listed Wyoming specifically in their distribution scope.

About recalls in Wyoming

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 Wyoming 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 20189

  • SevereFDA (Devices)·Z-2444-2024·2024-08-14

    Medline Procedure Kits Recalled Due to Defective Syringes and Quality Issues

    Medline procedure kits containing defective plastic syringes have been recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects over 1.6 million units distributed worldwide.

    Product
    Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ; 4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ; 5) ARTERIOGRAM PACK, Pack Number DYNJ5
    Category
    Medical Device
    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
  • 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-1663-2024·2024-08-14

    Palmer Patriotic Munchy Medley Recalled for Potential Salmonella Contamination

    Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.

    Product
    Palmer Patriotic Munchy Medley, Net Wt 15oz, UPC 7723237060, 12/15oz 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 (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 (Devices)·Z-2443-2024·2024-08-14

    Medline Procedure Kits Recalled Due to Defective Plastic Syringes

    Medline procedure kits containing defective plastic syringes are being recalled nationwide. The syringes may leak, break, or have other quality issues that could pose a risk to patient health.

    Product
    Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, Pack Number DYNJRA1221A
    Category
    Medical Device
    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-1654-2024·2024-08-14

    Al'Fez Natural Tahini Recalled for Potential Salmonella Contamination

    Al'Fez Natural Tahini in 5.6oz glass jars is being recalled due to potential Salmonella contamination. The recall affects 3,522 cases distributed nationwide.

    Product
    Al'Fez Natural Tahini in 5.6oz glass jars, UPC 711464506778
    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-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-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-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-1656-2024·2024-08-14

    Yogurt-Covered Pretzel Recall Due to Potential Salmonella Contamination

    Palmer & Company is recalling multiple yogurt-covered pretzel products distributed nationwide due to potential salmonella contamination. Consumers should not consume these products.

    Product
    1. Palmer Candy Classic Yogurt Pretzels, Net Wt 28 lbs, UPC 77232 10847 2. Sweet Smiles Yogurt Covered Pretzels, Net Wt. 3.25oz, UPC 77232 13641, 8/3.25oz case 3. Sconza Chocolates Yogurt Pretzels, Net Wt 14lbs, UPC 004166882015 4. Sunny Select Vanilla Yogurt Coated Pretzels, Net
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2508-2024·2024-08-14

    Philips IntelliVue Patient Monitor Software Missing Critical Entitlements

    Philips IntelliVue Patient Monitor models with software L.x and M.x lack critical monitoring capabilities due to a software update. This could result in incorrect or delayed patient treatment.

    Product
    IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866060. 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 (Drugs)·D-0630-2024·2024-08-14

    Estradiol Cypionate Injection Recalled Due to Lack of Sterility Assurance

    Empower Pharmacy is recalling Estradiol Cypionate Injection due to lack of assurance of sterility. The recall affects 2,797 units distributed nationwide within the United States.

    Product
    Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1669-2024·2024-08-14

    Favorite Day Bakery White Fudge Mini Cookies recalled for salmonella

    Favorite Day Bakery White Fudge Mini Cookies (7oz) recalled nationwide in the US and Canada due to potential salmonella contamination.

    Product
    Favorite Day Bakery White Fudge Mini Cookies, Net Wt 7oz, UPC 85239 92319, 16/7oz case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2524-2024·2024-08-14

    American Contract Systems Spine Pack kits recalled for insufficient sterilization aeration

    American Contract Systems is recalling Spine Pack convenience kits (Lot 980241) due to incomplete post-sterilization aeration. The affected kits were distributed in California, Kansas, Maine, Minnesota, Missouri, Nebraska, and South Dakota.

    Product
    American Contract Systems Spine Pack convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2485-2024·2024-08-14

    Automated medication cabinet software prints incorrect bin labels

    The BD PYXIS MEDBANK MINI automated dispensing cabinet software may print incorrect bin locations on restock labels, potentially causing medications to be placed in wrong locations.

    Product
    BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2532-2024·2024-08-14

    FDA Recalls CryoPatch Cardiac Tissue Grafts Due to Invalid Test Results

    Artivion has recalled CryoPatch SG cardiac tissue patches used in pulmonary surgeries due to approval and release with invalid test results. Patients who received implants should consult their healthcare provider.

    Product
    (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tis
    Category
    Medical Device
    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-2491-2024·2024-08-14

    BD PYXIS MEDBANK Cabinet Software Causes Incorrect Medication Labels

    FDA recall of BD PYXIS MEDBANK automated medication dispensing cabinets due to a software defect that prints incorrect bin information on restock labels, potentially leading to medication identification errors.

    Product
    BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2494-2024·2024-08-14

    Medication Dispensing Cabinet Software Defect Causes Incorrect Bin Labels

    BD PYXIS automated medication dispensing cabinets contain a software issue that may print incorrect bin locations on restock labels. This could result in medications being placed in the wrong bin during restocking.

    Product
    BD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2526-2024·2024-08-14

    Luminos dRF Max X-ray Display Support Arm May Unintentionally Lower

    Siemens recalled 24 units of the Luminos dRF Max X-ray display system because the support arm may unintentionally lower, potentially injuring personnel positioned beneath the equipment.

    Product
    Luminos dRF Max- Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762471
    Category
    Medical Device
    Distribution
    Distributed nationwide