The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

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251–275 of 778

  • HighFDA (Food)·H-0775-2026·2026-05-20

    Uncle Giuseppe's Milk Chocolate Bridge Mix recalled for undeclared allergens

    Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix (11 oz) is recalled due to undeclared allergens: cashews, milk, and soy. The product was distributed in New York and New Jersey with sell-by dates from September 4 to November 6, 2026.

    Product
    Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamper resistant plastic container. UPC 812235023309. Distributed by: WE R NUTS LLC, 99 Seaview Blvd, Port Washington, NY 11050
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0772-2026·2026-05-20

    Dakota Honey Company Spreadable Spun Honey Flight recalled for foreign objects

    Dakota Honey Company is recalling its Honey Flight spreadable spun honey in four flavors due to potential contamination with stainless steel dust, flakes, or plastic shreds.

    Product
    Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original - Salted Caramel - Cinnamon - Jalapeno. UPC 8 60010-57968 8. 4 - 4 oz (340g) jars. Net Wt 16 oz (454g). Produced in Winner, SD.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2194-2026·2026-05-20

    Daig Livewire Steerable Reprocessed Electrophysiology Catheters Recalled

    Stryker Sustainability Solutions is recalling Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product packaging. The defect may compromise sterility.

    Product
    Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0778-2026·2026-05-20

    Swad Mango Flavored Masala Candy recalled for undeclared Blue 1

    Raja Foods and Vegetables Inc. is recalling Swad Mango Flavored Masala Candy because it contains undeclared Blue 1 food coloring, which may cause an allergic reaction in sensitive individuals.

    Product
    Swad Mango Flavored Masala Candy
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2176-2026·2026-05-20

    Reprocessed Electrophysiology Catheter with Incomplete Sterile Seals

    Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200344) due to incomplete seals on sterile product packaging that could compromise sterility.

    Product
    BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2164-2026·2026-05-20

    [pending] Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App

    Pending LLM rewrite. Source: FDA_DEVICE Z-2164-2026.

    Product
    Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: Versions 2.9.0 through 2.11.2 Product Description: Dexcom G7 CGM watchOS App - The watchOS app is installed along with the iOS ph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2180-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Recalled for Incomplete Seals

    Stryker Sustainability Solutions is recalling BARD Dynamic XT Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product, which could compromise sterility.

    Product
    BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2165-2026·2026-05-20

    Dexcom ONE+ iOS CGM App Software Defect Delayed Glucose Alerts

    Dexcom, Inc. is recalling Dexcom ONE+ iOS CGM App versions 1.5.0 and 1.6.0 due to a software defect that can delay glucose alerts and notifications, risking delayed detection of low or high blood sugar events.

    Product
    Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: Dexcom ONE+ iOS CGM App Component: Dexcom ONE+ Continuous Glucose Monitoring Syste
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0773-2026·2026-05-20

    Alain MILLIAT Orange Marmalade 300g Recalled for Possible Glass Contamination

    Alain MILLIAT Orange Marmalade in 300g glass jars is being recalled because the product may contain glass fragments. Consumers should not consume the product and should discard it or return it.

    Product
    Alain MILLIAT; MARMELADE ORANGE; 300 g 10.6 oz; packaged in glass jars
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2185-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Recall Due to Incomplete Seals

    Stryker Sustainability Solutions is recalling 816 units of CS Uni-Directional w Auto ID reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.

    Product
    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2183-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Recalled for Incomplete Sterile Seals

    Stryker Sustainability Solutions is recalling 154 units of BW Webster Duo-Decapolar reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging, which may compromise sterility.

    Product
    BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2189-2026·2026-05-20

    Daig Livewire Steerable Electrophysiology Catheters Recalled for Incomplete Seals

    Stryker Sustainability Solutions is recalling Daig Livewire Steerable electrophysiology catheters with incomplete seals on sterile packaging. The defect may allow contamination of the sterile product.

    Product
    Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0774-2026·2026-05-20

    Frederik's by Meijer Vanilla Bourbon Trail Mix recalled for undeclared allergens

    Ferris Coffee and Nut Company is recalling Frederik's by Meijer Vanilla Bourbon Trail Mix because it contains undeclared wheat and soy allergens. The product was distributed to IL, IN, KY, MI, OH, and WI.

    Product
    Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2199-2026·2026-05-20

    Reprocessed Medtronic Marinr Steerable Electrophysiology Catheter Recall

    Stryker Sustainability Solutions is recalling 87 units of the Medtronic Marinr Steerable reprocessed electrophysiology catheter (Product Number 72402) due to incomplete seals on the sterile product.

    Product
    Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2181-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Recalled for Incomplete Sterile Seals

    Stryker Sustainability Solutions is recalling 217 units of BARD EP XT Decapolar Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.

    Product
    BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2187-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Recall Due to Incomplete Sterile Seals

    Stryker Sustainability Solutions is recalling 108 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging. The defect may compromise sterility assurance.

    Product
    Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2201-2026·2026-05-20

    Medtronic SynchroMed Flex Infusion Programmer Software Application

    Medtronic SynchroMed Flex Infusion Mode A810 Clinician Programmer Software may display infusion steps out of order, preventing medication from being delivered at the intended time. Affected devices are clinician programmer tablets worldwide.

    Product
    Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900A; 2. PROG CT900B CLINICIAN TABLET EU -UK, Model Number CT900B; 3. PROG CT900C CLINICIAN TABLET
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2169-2026·2026-05-20

    QuickVue Dipstick Strep A Test Recalled for False Positive Results

    Quidel Corporation is recalling the QuickVue Dipstick Strep A Test (50T, REF 20108) due to the potential for false positive results. The product was distributed nationwide.

    Product
    QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0769-2026·2026-05-20

    Dakota Honey Company Spreadable Spun Honey Cinnamon-Infused Recall

    Dakota Honey Company is recalling Spreadable Spun Honey, Cinnamon-Infused, in 4 oz and 12 oz jars due to potential foreign objects including stainless steel dust, flakes, or plastic shreds. Consumers should stop using affected jars purchased during the specified timeframes.

    Product
    Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41980 7. 2. Net Wt 12 oz (340g) UPC 8 60010-57963 3.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2198-2026·2026-05-20

    Daig Livewire Steerable BDB Electrophysiology Catheter Recall

    Stryker Sustainability Solutions is recalling Daig Livewire Steerable BDB reprocessed electrophysiology catheters due to incomplete seals on the sterile product.

    Product
    Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2179-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Recalled for Incomplete Seals

    Stryker Sustainability Solutions is recalling BARD Dynamic XT Steerable reprocessed electrophysiology catheters (Product Number 201103) due to incomplete seals on the sterile product packaging.

    Product
    BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2175-2026·2026-05-20

    BARD Dynamic Tip Steerable Reprocessed Electrophysiology Catheter Recall

    Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200131) due to incomplete seals on sterile product packaging. The recall affects 61 units distributed nationwide in the US and in Israel and Canada.

    Product
    BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2188-2026·2026-05-20

    Reprocessed Electrophysiology Catheter Daig Livewire Steerable recalled

    Stryker Sustainability Solutions is recalling Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product. The recall affects 19 units distributed nationwide in the US, Israel, and Canada.

    Product
    Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide