State

Michigan product recalls

73,388 recalls have nationwide distribution and so reach Michigan. 9,548 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total: 9,548
Critical: 1,566
Severe: 2,549
Most recent: 2026-09-25

Of the 9,548 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 2,549 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,548 recalls whose distribution notice names Michigan specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18501–18525 of 82936

HighFDA (Food)·F-0438-2023·2023-03-22
Chocolate Baking Chips Recalled Due to Undeclared Peanut Residue
Clasen Quality Chocolater has recalled 4M DF NSA Semisweet Baking Drop chocolate due to potential undeclared peanut residue. The product may pose a risk to consumers with peanut allergies.
Product
4M DF NSA Semisweet Baking Drop (FT), Item # 56854. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Chocolate Liquor, Inulin, Erythritol, Cocoa Butter, Sunflower Lecithin (an emulsifier), Vanilla Extract, Stevia Leaf Reb M. Distributed By: Clasen Quality…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0437-2023·2023-03-22
Dark Chocolate Wafer Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater is recalling DF Dark Choc Flvd Wafer (Item #56810) in 50-pound cases because the product may contain undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
DF Dark Choc Flvd Wafer (MB), Item # 56810. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernel Oil, Cocoa Powder (processed with Alkali), Sunflower Lecithin (an emulsifier), Salt. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0428-2023·2023-03-22
White Confectionery Coating Wafer Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater is recalling 20,360 lbs of white confectionery coating wafer due to possible undeclared peanut residue that poses a risk to consumers with peanut allergies.
Product
White Confectionery Coating Wafer (HP, NSA), Item # 52544. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Palm Kernal Oil, Whey Protein Isolate, Erythritol, Sodium Caseinate, Sunflower Lecithin (an emulsifier), Salt, and Sucralose. Distributed By: Clasen Quality…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0583-2023·2023-03-22
Celestial Seasonings Mandarin Orange Spice Tea Contains Undeclared Caffeine
Celestial Seasonings Mandarin Orange Spice herbal tea K-cups contain undeclared caffeine from black tea. The recall affects 1,844 units distributed nationwide.
Product
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Category
Food
Distribution
42 states
HighFDA (Devices)·Z-1249-2023·2023-03-22
Plato 17 Microcatheter Recalled Due to Loose Particle Risk
Scientia Vascular is recalling Plato 17 Microcatheters due to manufacturing defects that may introduce loose particles into the catheter lumen, potentially causing blood vessel blockage or inflammatory reactions.
Product
Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1255-2023·2023-03-22
Medical Device Apheresis Kit Recalled Due to Stress Leak Risk
Fenwal Inc is recalling 6,564 units in certain lots of Amicus apheresis kits because centrifuge packs may develop a stress leak. No illnesses or injuries have been reported.
Product
Amicus Exchange Kit Therapeutics. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1250-2023·2023-03-22
Arial mobile application recalled for Android loading failures
Securitas Healthcare is recalling the Arial mobile application for Android devices because the app does not load or function properly. Users should stop using the app immediately.
Product
Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0436-2023·2023-03-22
Chocolate Confectionery Drops Recalled Due to Undeclared Peanut Residue
Clasen Quality Chocolater is recalling 4M Cinnamon Flvd Confectionery Drops because the chocolate may contain undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
4M Cinnamon Flvd Confectionery Drop (MB), Item # 56466. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernel Oil, Nonfat Dry Milk, Ground Cinnamon, Sunflower Lecithin (an emulsifier). Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0432-2023·2023-03-22
Clasen Semisweet Chocolate Drops Recalled for Undeclared Peanut
Clasen Quality Chocolate recalled 2M Semisweet Chocolate Drops due to undeclared peanut residue. Approximately 150,600 lbs distributed across 12 states.
Product
2M Semisweet Chocolate Drop, Item # 53700. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Unsweetened Chocolate, Sugar, Cocoa Butter, Dextrose, Sunflower Lecithin (an emulsifier), and Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
Category
Food
Distribution
12 states
HighFDA (Drugs)·D-0463-2023·2023-03-22
Clobazam Tablets Recalled Due to Cross Contamination Risk
Breckenridge Pharmaceutical is recalling Clobazam 20 mg tablets (Lot #5210147, exp. 12/2023) nationwide due to potential cross contamination from manufacturing deviations.
Product
Clobazam Tablets, 20 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-901-01
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V188000·2023-03-22
Volvo Recalls 2023 Models for False Emergency Call System Warnings
Volvo is recalling 2023 S60, C40, XC40, V60CC, XC60, and XC90 vehicles because a false warning may mask an actual emergency call system failure.
Product
VOLVO — VOLVO S60, C40BEV, XC40, V60CC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1262-2023·2023-03-22
da Vinci Surgical System Patient Cart Ballscrew Failure Risk
Intuitive Surgical recalls Patient Side Carts for da Vinci X and Xi surgical systems due to ballscrew failure risk. The failure could cause uncontrolled carriage movement leading to potential tissue injury during surgery. 9 units affected.
Product
Patient Side Cart, REF: 380620, with instrument arms, used as part of the da Vinci X Surgical System, REF: IS4200; Patient Side Cart, REF: 380652, with instrument arms, used as part of the da Vinci Xi Surgical System, REF: IS4000
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V190000·2023-03-22
Alexis Fire Equipment Recalls 2022 Fire Apparatus Due to Winch Remote Defect
Alexis Fire Equipment is recalling 2022 fire apparatus vehicles because water may enter the winch remote, causing corrosion and unintentional winch operation.
Product
ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1241-2023·2023-03-22
BD Insulin Syringes Recalled for Potential Nonsterile Condition
Becton Dickinson & Company is recalling 1.17 million BD Ultra-Fine Insulin Syringes due to a nonsterile manufacturing defect that could expose patients to pathogenic microorganisms and increase infection risk.
Product
BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326678
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1222-2023·2023-03-22
Hair Growth Laser Comb Recalled for Missing Safety Warnings and Labels
OMM Imports' Recreo Hair Growth Laser Comb is being recalled because 1,620 units lack required safety labels, warnings, and certification documentation. Missing labels create risk for users of the Class 3R laser device.
Product
Recreo Hair Growth Laser Comb
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0442-2023·2023-03-22
Chocolate wafer product recalled for undeclared peanut residue
Clasen Quality Chocolate is recalling DF ANSA chocolate wafers because the product may contain undeclared peanut residue, posing a risk to consumers with peanut allergies.
Product
DF ANSA Choc Flvd Conf Wafer (MB), Item # 59154. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Soluble Corn Fiber, Palm Kernel and Palm Oil, Allulose, Cocoa Powder (Processed with Alkali), Chocolate Liquor, Sunflower Lecithin (an emulsifier), Monk Fruit Extract.…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0441-2023·2023-03-22
38% Cacao Milk Chocolate Wafers Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater has recalled 38% Cacao Milk Chocolate Wafers due to undeclared peanut residue. Consumers with peanut allergies should not consume the product.
Product
38% Cacao Milk Chocolate Wafer (RA MB), Item # 58873. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Cocoa Butter, Milk, Chocolate Liquor, Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1259-2023·2023-03-22
Radiation Therapy Software May Not Properly Execute Heart-Protection Breath Hold
Brainlab ExacTrac Dynamic software used in charged-particle radiation therapy systems may not properly execute Deep Inspiration Breath Hold (DIBH) functionality, a heart-protection technique. The issue affects 56 systems across the United States.
Product
Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0443-2023·2023-03-22
NGMO Ballard Semisweet Chocolate Wafer Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater is recalling NGMO Ballard Semisweet Chocolate Wafer due to possible undeclared peanut residue. Consumers with peanut allergies who may have purchased this product should not consume it.
Product
NGMO Ballard Semisweet Chocolate Wafer, Item # 59343. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Chocolate Liquor (Processed with Alkali), Sugar, Cocoa Butter, Butterfat (Milk), Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1256-2023·2023-03-22
Ambulance cot may separate due to insufficient epoxy in assemblies
Stryker's Power-PRO 2 ambulance cots may separate at head or foot due to insufficient epoxy. Four affected units in NY and VA should be removed from service immediately.
Product
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1260-2023·2023-03-22
Bard Mission Disposable Core Biopsy Instrument Kit Recall: Sizing Incompatibility
Bard Peripheral Vascular is recalling certain Bard Mission Disposable Core Biopsy Instrument Kits due to sizing incompatibility between the biopsy instrument and coaxial needle, which could cause procedural delays or needle breakage.
Product
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1238-2023·2023-03-22
BD Insulin Syringes Recalled Due to Nonsterile Condition
BD Insulin Syringes (Catalog 329420) are being recalled due to nonsterile conditions that could expose patients to pathogenic microorganisms and increase infection risk. The recall affects 961,000 units distributed worldwide.
Product
BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml, 12.7mm, 28G Single Unit Scale. Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329420
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0610-2023·2023-03-22
Soybean Lecithin Powder Recalled for Undeclared Peanut Allergen
Navada Imports is recalling 575 cases of soybean lecithin powder due to undeclared peanut allergen. Affected products were distributed nationwide to manufacturers.
Product
Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0607-2023·2023-03-22
Sunflower Lecithin Powder Recalled for Undeclared Peanut Allergen
Navada Imports is recalling sunflower lecithin powder in 44 lb. boxes due to an undeclared peanut allergen. The affected product poses a serious risk to consumers with peanut allergies.
Product
Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1251-2023·2023-03-22
BioFire BCID2 Diagnostic Panels Recalled for Temperature-Related Performance Issues
BioFire Diagnostics is recalling BioFire BCID2 diagnostic panels that experienced temperature excursions during shipment, which may reduce their performance. Affected kits were distributed in Florida and Georgia.
Product
In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147
Category
Medical Device
Distribution
Distributed nationwide