The Recall Desk

State

Michigan product recalls

72,984 recalls have nationwide distribution and so reach Michigan. 9,518 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total
9,518
Critical
1,556
Severe
2,145
Most recent
2026-09-16

Of the 9,518 recalls naming Michigan we have scored against our rubric, 1,556 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,145 (23%) are Severe.

These figures cover only the 9,518 recalls whose distribution notice names Michigan specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6126–6150 of 82502

  • SevereFDA (Food)·H-0322-2025·2025-07-30

    SunBiotics probiotic chocolate covered almonds tested positive for Salmonella

    SunBiotics Activated Almonds Infused with Probiotics, Oat Milk Chocolate, are being recalled after the firm detected Salmonella on one batch. 196 units are affected.

    Product
    SunBiotics Activated Almonds Infused with Probiotics, Oat Milk Chocolate, NET WT. 1 oz(28g) packaged in cases.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·H-0319-2025·2025-07-30

    Artisan style half loaves recalled over undeclared hazelnut from mispackaging

    Artisan Style 1/2 Loaf white bread is being recalled because product containing hazelnuts was put in bags whose allergen statement does not include hazelnuts. 883 loaves are affected.

    Product
    Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two splits on top 7/13/2025 - Best By Flexible plastic bag
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2136-2025·2025-07-30

    Endosee system convenience trays label non-sterile iodine pouches as sterile

    Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.

    Product
    Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2137-2025·2025-07-30

    Endosee convenience kits label non-sterile iodine pouches as sterile

    Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.

    Product
    Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2134-2025·2025-07-30

    Azurion 7 M20 C-arm gearbox mounting bolts may become loose

    The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.

    Product
    Azurion 7 M20. Fluoroscopic X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0325-2025·2025-07-30

    Ritz cracker sandwich variety packs recalled over undeclared peanut from mispackaging

    Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.

    Product
    Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38 oz Packs) Net Wt. 27.3 oz (20-1.38 oz packet of cracker sandwiches inside cartons of varying sizes). 20-27.3 OZ (Case: 6 - 27.3 Oz Cartons in master carton. UP
    Category
    Food
    Distribution
    49 states
  • HighFDA (Drugs)·D-0535-2025·2025-07-30

    Compounded epinephrine lidocaine vials returned subpotent assay results in stability testing

    Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.

    Product
    Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0541-2025·2025-07-30

    Budesonide inhalation ampoules recalled after leakage and empty ampoule complaint

    Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.

    Product
    BUDESONIDE — BUDESONIDE (BUDESONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2025·2025-07-30

    EMPOWR dual mobility poly bearings were packaged with the wrong implant

    EMPOWR Acetabular Dual Mobility Poly Bearings are being recalled because of a packaging discrepancy in which incorrect implants were packaged, discovered through a customer complaint. 20 units affected.

    Product
    Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catalog Number: 952-28-40E Software Version: NA Product Description: The EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femora
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-2148-2025·2025-07-30

    EMPOWR dual mobility OD42 bearings were packaged with the wrong implant

    EMPOWR Acetabular Dual Mobility Poly Bearings, catalog number 952-28-42F, are being recalled because of a packaging discrepancy in which incorrect implants were packaged. 20 units affected.

    Product
    Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 Model/Catalog Number: 952-28-42F Software Version: NA Product Description: The EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femora
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-2130-2025·2025-07-30

    SIGNA Architect gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA Architect MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA Architect
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2025·2025-07-30

    SIGNA PET/MR gradient coils can produce acoustic noise above the limit

    GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA PET/MR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0314-2025·2025-07-30

    Turkeyfoot Creek Creamery mocha artisan ice cream has undeclared soy

    Turkeyfoot Creek Creamery Mocha Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Mocha Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2131-2025·2025-07-30

    SIGNA Architect AIR gradient coils can produce acoustic noise above limit

    GE HealthCare SIGNA Architect AIR MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.

    Product
    SIGNA Architect AIR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0312-2025·2025-07-30

    Turkeyfoot Creek Creamery cookie dough ice cream has undeclared soy and wheat

    Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cookie Dough Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·25V497000·2025-07-30

    Brinkley trailer wiring may be unsecured risking a short circuit

    Brinkley RV is recalling certain 2025 Model Z trailers because the electrical wiring may not be secured properly, which can damage the wiring and cause a short circuit.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0310-2025·2025-07-30

    Turkeyfoot Creek Creamery brownie ice cream has undeclared soy and wheat

    Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cacao Brownie Bites Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0311-2025·2025-07-30

    Turkeyfoot Creek Creamery cookies and cream ice cream has undeclared allergens

    Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cookies and Cream Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0309-2025·2025-07-30

    Turkeyfoot Creek Creamery chocolate peanut butter ice cream has undeclared soy

    Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Chocolate Peanut Butter Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0326-2025·2025-07-30

    Ritz peanut butter cracker sandwiches recalled over undeclared peanut from mispackaging

    Ritz Peanut Butter Cracker Sandwiches are being recalled because of undeclared peanut allergens due to mispackaging. 37,985 units are affected across nearly every state.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 14X8-Case: 14 - 11.04 Oz Cartons in master carton. UPC 0 44000 88210 5
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·H-0323-2025·2025-07-30

    Ritz peanut butter cracker 20 count cartons recalled over undeclared peanut

    Ritz Peanut Butter Cracker Sandwiches in 27.6 oz 20 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 24,446 cases are affected.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside cartons. And 6x20(6 - 27.6 oz Cartons) in master carton. UPC 1 00 44000 07584 2
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-2171-2025·2025-07-30

    Stryker StrykeFlow irrigator with tip may leak solution into handpiece

    The Stryker StrykeFlow Disposable Suction/Irrigator with Disposable Tip is being recalled because irrigation solution may leak into the handpiece and battery pack, causing it to malfunction.

    Product
    Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0308-2025·2025-07-30

    Turkeyfoot Creek Creamery Avalanche ice cream has undeclared soy and wheat

    Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy and wheat. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0324-2025·2025-07-30

    Ritz peanut butter cracker 40 count cartons recalled over undeclared peanut

    Ritz Peanut Butter Cracker Sandwiches in 55.2 oz 40 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 224 cases are affected.

    Product
    Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton. 40 - 55.2oz Cartons in master carton. UPC 0 44000 07819 5
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·H-0315-2025·2025-07-30

    Turkeyfoot Creek Creamery cacao strawberry ice cream has undeclared soy

    Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream in one pint cartons is being recalled because of undeclared soy. All expiration dates are affected.

    Product
    Turkeyfoot Creek Creamery Cacao Strawberry Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with paper lid
    Category
    Food
    Distribution
    3 states