The Recall Desk

State

Michigan product recalls

72,820 recalls have nationwide distribution and so reach Michigan. 9,516 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total
9,516
Critical
1,556
Severe
2,143
Most recent
2026-09-02

Of the 9,516 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 2,143 (23%) are Severe.

These figures cover only the 9,516 recalls whose distribution notice names Michigan specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

151–175 of 82336

  • CriticalFDA (Food)·H-1248-2026·2026-08-26

    Whole Foods Spicy Guacamole Dip Recalled for Potential Salmonella Contamination

    Whole Foods Market is recalling Spicy Guacamole Dip No Tomatoes because the jalapeños used may be contaminated with Salmonella. The product was sold in 13 states.

    Product
    Whole Foods Spicy Guacamole Dip No Tomatoes, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 25745200000, 284324000000, 2350
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-1249-2026·2026-08-26

    Whole Foods Guacamole Recalled for Potential Salmonella Contamination

    Whole Foods Market is recalling Medium Pico de Gallo Guacamole Dip because it may contain jalapenos contaminated with Salmonella.

    Product
    Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 29802800000. Packed for Wh
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-1253-2026·2026-08-26

    Whole Foods Trio Dip Recalled Due to Potential Salmonella Contamination

    Whole Foods Trio Dip is being recalled because the jalapeños used in the product may be contaminated with Salmonella.

    Product
    Whole Foods Trio Dip, Contains Pico de Gallo, Guacamole, Salsa. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 25926000000
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-1252-2026·2026-08-26

    Whole Foods Spicy Guacamole Dip Recalled for Salmonella Risk

    Whole Foods Market is recalling Spicy Guacamole Dip because the jalapenos used may be contaminated with Salmonella.

    Product
    Whole Foods Spicy Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 21212000000, 21211900000, 25138200000. Pa
    Category
    Food
    Distribution
    13 states
  • CriticalFDA (Food)·H-1257-2026·2026-08-26

    Get Fresh Produce Jalapeno Peppers Recalled for Potential Salmonella Contamination

    Get Fresh Produce is recalling jalapeno peppers due to potential Salmonella contamination. The product was distributed in Illinois, Indiana, Michigan, and Wisconsin.

    Product
    Get Fresh Produce Jalapeno Peppers. Item 01896 - 2 lb. box; Item 01894 - 10 lb. box
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-1250-2026·2026-08-26

    Whole Foods Pomegranate Guacamole Dip Recalled for Potential Salmonella Contamination

    Whole Foods Market is recalling Pomegranate Guacamole Dip because it may contain jalapenos contaminated with Salmonella. The product was sold in 13 states.

    Product
    Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 27908100000, 27908500000. Packed fo
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0794-2026·2026-08-26

    Aminocaproic Acid Injection Recalled for Particulate Matter Contamination

    American Regent, Inc. is recalling Aminocaproic Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    AMINOCAPROIC ACID — AMINOCAPROIC ACID (AMINOCAPROIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0791-2026·2026-08-26

    American Regent Recalls Nitroglycerin Injection Due to Particulate Matter

    American Regent, Inc. is recalling Nitroglycerin injection vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    NITROGLYCERIN — NITROGLYCERIN (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0796-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Acetylcysteine Solution, USP, 10% due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0801-2026·2026-08-26

    American Regent Recalls Tralement Injection Due to Particulate Matter

    American Regent is recalling 323,000 vials of Tralement (trace elements injection 4) due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    TRALEMENT — TRALEMENT (TRACE ELEMENTS INJECTION 4)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2960-2026·2026-08-26

    Tobii Dynavox Recalls TD Navio Maxi Speech Generating Devices

    Tobii Dynavox is recalling TD Navio Maxi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.

    Product
    TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0764-2026·2026-08-26

    Shilpa Medicare Recalls Discolored Pemetrexed Injection Vials

    Shilpa Medicare is recalling 18,434 vials of PEMRYDI RTU (pemetrexed injection) due to reports of green to dark green discoloration in the solution.

    Product
    PEMRYDI RTU — PEMRYDI RTU (PEMETREXED DISODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0795-2026·2026-08-26

    American Regent Recalls Atropine Sulfate Injection Due to Particulate Matter

    American Regent, Inc. is recalling Atropine Sulfate injection vials because they contain particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ATROPINE SULFATE — ATROPINE SULFATE (ATROPINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2975-2026·2026-08-26

    Siemens Quinidine Assay Recalled for Precision Errors

    Siemens is recalling 20 units of the Syva EMIT 2000 Quinidine Assay due to precision issues that may cause inaccurate test results.

    Product
    Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL, 1x14mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2976-2026·2026-08-26

    Siemens Recalls Emit 2000 Quinidine Assay Due to Precision Issues

    Siemens Healthcare Diagnostics is recalling specific lots of the Emit 2000 Quinidine Assay because unacceptable precision may cause falsely high results, risking improper patient treatment.

    Product
    Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0793-2026·2026-08-26

    American Regent Recalls Cyanocobalamin Injections Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0797-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0802-2026·2026-08-26

    FDA Recalls Nicardipine Hydrochloride Injection Due to Particulate Matter

    American Regent, Inc. is recalling 43,460 vials of Nicardipine Hydrochloride Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    NICARDIPINE HYDROCHLORIDE — NICARDIPINE HYDROCHLORIDE (NICARDIPINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2959-2026·2026-08-26

    Tobii Dynavox Recalls TD Navio Midi Speech Generating Devices

    Tobii Dynavox is recalling TD Navio Midi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.

    Product
    TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2983-2026·2026-08-26

    Fort Defiance Automated Field Steam Sterilizer Recalled for Electrical Grounding Defect

    Fort Defiance Industries is recalling Automated Field Steam Sterilizers because a water recovery system connector may lose ground continuity, creating an unreliable fault current return path.

    Product
    Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
    Category
    Medical Device
    Distribution
    Distributed nationwide