The Recall Desk

State

Michigan product recalls

73,509 recalls have nationwide distribution and so reach Michigan. 9,551 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total
9,551
Critical
1,566
Severe
2,550
Most recent
2026-10-24

Of the 9,551 recalls naming Michigan we have scored against our rubric, 1,566 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,550 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,551 recalls whose distribution notice names Michigan specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21801–21825 of 83060

  • HighFDA (Devices)·Z-1431-2022·2022-07-27

    BD Connecta Infusion Stopcock Recall Due to Potential Housing Leakage

    BD Connecta Stopcock infusion devices may leak at the housing component, potentially delaying or interrupting treatment and exposing patients to biohazardous material. The recall affects 485,000 units distributed worldwide.

    Product
    BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1427-2022·2022-07-27

    GE Anesthesia Systems Base Cracking and Fall Hazard Recalled

    GE Healthcare anesthesia systems may develop cracks in the base, potentially causing the device to tip and fall. The FDA recalled 667 units distributed across multiple U.S. states and countries.

    Product
    GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.
    Category
    Medical Device
    Distribution
    28 states
  • HighFDA (Devices)·Z-1447-2022·2022-07-27

    Aesculap S4 Cervical Cross Connector Recalled Due to Clamping Force Defect

    Aesculap Implant Systems is recalling the S4 Cervical Cross Connector L 33-42mm due to insufficient clamping force that may cause connector movement or microparticle abrasion in spinal fusion implants.

    Product
    AESCULAP S4 Cervical Cross Connector L 33-42mm, S4C CROSS CONNECTOR VARIABLE 33-42MM, product code SW116T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1473-2022·2022-07-27

    Honey Caramels Butterscotch Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Butterscotch due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.

    Product
    Honey Caramels Butterscotch. Net wt. 5.87 oz. PLU Code: 788394 12675 8. Ingredients: Honey, Butter (Pasteurized Cream & Salt), Cream, Grade A Non-Fat Dry Milk, Whey, Natural Flavors, Agar, Algin and Lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1269-2022·2022-07-27

    FDA Recalls Nephron Cardioplegia Solution Over Sterility Assurance Concerns

    Nephron Sterile Compounding Center is recalling del Nido Cardioplegia Solution due to lack of assurance of sterility. The 1765 bags affected were distributed nationwide.

    Product
    del Nido Cardioplegia Solution 1000 mL (1000 mL) Single-Dose Container IV bag, 4 x 1 IV Bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-984-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1275-2022·2022-07-27

    Phenylephrine HCl injection recalled for lack of sterility assurance

    Nephron Sterile Compounding Center recalls Phenylephrine HCl Injection syringes nationwide due to lack of sterility assurance. Patients with affected lots should contact their healthcare provider.

    Product
    Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 mcg/mL)syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-956-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1441-2022·2022-07-27

    Espresso Cheesecake Bites recalled due to undeclared soy lecithin

    Chuckanut Bay Foods is recalling Espresso Cheesecake Bites because the product contains undeclared soy lecithin. The label states sunflower lecithin, but soy—a major allergen—is actually present.

    Product
    Item 32023-56, Chuckanut Bay Espresso Cheesecake Bites (Dark Compound) BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. Item 35023-12, Espresso Cheesecake Bites. Edible brand. Distributed by Wish Foods, LLC. Perishable - Keep…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Drugs)·D-1280-2022·2022-07-27

    Anticoagulant Sodium Citrate Solution Recalled for Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling 85,300 pre-filled syringes of Anticoagulant Sodium Citrate Solution due to failure to assure sterility. Affected patients should contact their healthcare provider.

    Product
    Anticoagulant Sodium Citrate Solution, USP 4%, 200 mg/5 mL (40 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-906-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1448-2022·2022-07-27

    Cervical spinal implant connectors may fail to maintain proper clamping force

    Aesculap Implant Systems has recalled certain cervical spine implant connectors due to insufficient clamping force. The defect may allow movement on the rods or cause microparticle abrasion.

    Product
    AESCULAP S4 Cervical Cross Connector L 42-58mm, S4C CROSS CONNECTOR VARIABLE 42-58MM, product code SW117T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1443-2022·2022-07-27

    Cheesecake Bites Recalled for Undeclared Soy Lecithin Allergen

    Chuckanut Bay Cheesecake Bites Lemon are being recalled due to undeclared soy lecithin in the product. The label incorrectly lists sunflower lecithin as an ingredient, posing a risk to consumers with soy allergies.

    Product
    Item 34032-12, Chuckanut Bay Cheesecake Bites Lemon. Perishable - Keep Refrigerated. There are 8 pieces per pack and 12 packs per case. Net Wt. 6.4 oz. UPC 6 03812 34032 8. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, CHOCOLATE COMPOUND (sunflower…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1435-2022·2022-07-27

    BD Connecta Stopcock Without Extension Tube Recalled for Potential Leakage Risk

    Becton Dickinson & Company is recalling BD Connecta Stopcock units worldwide due to a potential housing leakage defect that could interrupt treatment or cause exposure to biohazardous material.

    Product
    BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1416-2022·2022-07-27

    Hill-Rom Centrella Pro+ mattress reduced heat-moisture management performance

    Affected Hill-Rom Centrella Pro+ 36-inch mattresses may have reduced Microclimate Management performance, increasing risk of pressure ulcer development. The failure affects heat and moisture control.

    Product
    Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1251-2022·2022-07-27

    Epinephrine Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 134,385 epinephrine injection syringes nationwide due to lack of assurance of sterility. No illnesses have been reported.

    Product
    EPINEPHrine Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1276-2022·2022-07-27

    Nephron Phenylephrine HCl Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center LLC recalls Phenylephrine HCl Injection (1 mg/10 mL) syringes nationwide due to inability to guarantee sterility. Approximately 464,265 syringes across eleven lot numbers are affected.

    Product
    Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-957-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1268-2022·2022-07-27

    Morphine Sulfate Injection Recalled Due to Sterility Assurance Concerns

    Nephron Sterile Compounding Center LLC is recalling morphine sulfate injection syringes due to lack of assurance of sterility. The recall affects 4,620 pre-filled syringes distributed nationwide.

    Product
    Morphine Sulfate Injection, USP, 1 mg/mL syringe, packaged in 5 x 1 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1403-2022·2022-07-27

    Radiation treatment planning software fails to propagate treatment course data

    RayStation 9B SP1 radiation treatment planning software has an issue where treatment course information may not be propagated to other systems in some workflows. This could potentially affect treatment planning accuracy.

    Product
    RayStation 9B SP1. For radiation treatment planning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1496-2022·2022-07-27

    Truffle Dark Gift Box Recalled for Undeclared Tree Nuts

    Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.

    Product
    Truffle Dark Gift Box, 12 pc., 6 oz. PLU Code: 788394 17660 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1486-2022·2022-07-27

    Honeymoons Dark Chocolate Cashew Recalled for Undeclared Tree Nuts

    Honeymoons Dark Chocolate Cashew products may contain undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product is being recalled from Queen Bee retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoons Dark Chocolate Cashew. PLU Code: 788394 14864 4.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1488-2022·2022-07-27

    Honeymoons Milk Chocolate Pecan recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoons Milk Chocolate Pecan candies due to the potential presence of undeclared tree nuts. Consumers with tree nut allergies should not consume this product.

    Product
    Honeymoons Milk Chocolate Pecan. PLU Code: 788394 14684 8. Ingredients: Honey, milk chocolate (sugar, milk, cocoa butter, chocolate liquor, sunflower lecithin and pure vanilla), pecans, butter (pasteurized cream, salt) cream, nonfat dry milk, whey, sunflower lecithin, algin…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1283-2022·2022-07-27

    FDA Recalls Cipla Difluprednate Eye Drops for Defective Container Caps

    Cipla is recalling 8,136 bottles of Difluprednate ophthalmic emulsion nationwide due to defective container caps that can break and expose the medication tip, compromising sterility.

    Product
    DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1433-2022·2022-07-27

    BD Connecta Stopcock Recalled for Potential Housing Leakage

    Becton Dickinson is recalling approximately 1.96 million BD Connecta Stopcock devices due to potential leakage at the housing component, which could interrupt treatment and expose patients to biohazardous material.

    Product
    BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1498-2022·2022-07-27

    Chocolate Sampler product recalled due to undeclared tree nuts

    Queen Bee Gardens is recalling Chocolate Sampler 13 oz packages due to undeclared tree nuts. The products may contain pecans, almonds, coconut, macadamia nuts, or walnuts.

    Product
    Chocolate Sampler Net wt. 13 oz. PLU Code: 788394 76511 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1442-2022·2022-07-27

    Chuckanut Bay Key Lime Cheesecake Bites Recalled for Undeclared Soy

    Chuckanut Bay Foods LLC recalls Key Lime Cheesecake Bites (Item 32012-56, Lot 2C168A2) because the label fails to declare soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Item 32012-56, Chuckanut Bay Key Lime Cheesecake Bites (Dark Compound) BULK. Perishable - Keep Refrigerated. There are 14 pieces per pack and 56 packs per case. The label is read in parts: BUTTER OIL, ENRICHED FLOUR (wheat flour ***), CRYSTALLIZED LIME***, SALT, CAROB BEAN…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1443-2022·2022-07-27

    Spinal Fusion Implant Cross Connectors Recalled for Insufficient Clamping Force

    Aesculap is recalling its S4 Cervical Cross Connector used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to move on the rods or shed particles.

    Product
    AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1462-2022·2022-07-27

    Macadamia Classic Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Macadamia Classic Truffles because they may contain undeclared tree nuts including almonds, coconut, and walnuts. The product poses allergen risks to consumers with tree nut allergies.

    Product
    Macadamia Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11060 3. Ingredients: Milk chocolate (sugar, milk, cocoa butter, chocolate liquor, soya lecithin and pure vanilla) honey, butter (pasteurized cream, salt), cream, roasted & sea salted macadamias, pecans, non-fat dry…
    Category
    Food
    Distribution
    Distributed nationwide