Michigan FDA Recalls — Food, Drug, and Medical Device (Past 90 Days)
Source: U.S. Food and Drug Administration (FDA) · openFDA Enforcement API · trailing 90-day window
65
Total active
25
Food
20
Drug
20
Medical Device
What "class" means
The FDA assigns every recall one of three classes based on the severity of harm if a person uses the product:
Class I
Reasonable probability of serious adverse health consequences or death. Stop using immediately and follow return instructions.
Class II
Use may cause temporary or medically reversible adverse effects. Probability of serious harm is remote.
Class III
Not likely to cause adverse health effects — usually quality, labeling, or minor purity issues.
🥗 Food Recalls
Apr 30, 2026
H-0780-2026
...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz);
Recalled by Ocinet, Inc.
Undeclared allergen ingredient (fish)
Apr 27, 2026
H-0779-2026
Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO p
Recalled by Prospector Popcorn, LLC
Products contain undeclared soy, specifically soy lecithin.
Apr 26, 2026
H-0781-2026
Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIB
Recalled by Sugar Foods LLC
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufactur
Apr 23, 2026
H-0761-2026
Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.
Recalled by Target Corporation
Undeclared allergens (sesame and soy)
Apr 22, 2026
H-0712-2026
french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET W
Recalled by French Broad Chocolate Factory
Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Waln
Apr 22, 2026
H-0685-2026
Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refri
Recalled by King Juice Company, Inc.
Product contains undeclared Yellow No. 5.
Apr 21, 2026
H-0837-2026
Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag
Recalled by Givaudan Flavors Corp
Product has the potential to be contaminated with Salmonella.
Apr 20, 2026
H-0774-2026
Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag N
Recalled by Ferris Coffee and Nut Company, Inc.
Undeclared allergens (wheat and soy).
Apr 20, 2026
H-0694-2026
Woodstock Organic Shelled Edamame 10 oz. and 48 oz.
Recalled by Green Organic Vegetables
Foreign object: metal pieces
Apr 19, 2026
H-0699-2026
Low Heat Non-Fat Dried Milk Powder - paper bags 25 kg. (packed under 5 labels: Off Grade
Recalled by California Dairies Inc.
Potential contamination with Salmonella.
Apr 19, 2026
H-0775-2026
Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamp
Recalled by WE R NUTS
Contains undeclared allergens (cashews, milk, and soy).
Apr 19, 2026
H-0698-2026
Low Heat Non-Fat Dried Milk Powder - plastic totes (NTE) 2200 lbs. (packed under 5 labels
Recalled by California Dairies Inc.
Potential contamination with Salmonella.
Apr 19, 2026
H-0684-2026
My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 oz; 6 pieces per container. UP
Recalled by The Mochi Ice Cream Company, LLC
Foreign object found inside retail container.
Apr 19, 2026
H-0700-2026
Buttermilk Powder - paper bags 25 kg. (packed under 1 label: BMP Extra Grade Standard)
Recalled by California Dairies Inc.
Potential contamination with Salmonella.
Apr 15, 2026
H-0679-2026
Negita Cracker- Shrimp 2.8oz
Recalled by Hadson (Toko) Trading Co. Inc.
Contains undeclared FD&C Yellow 6
Apr 15, 2026
H-0776-2026
Publix Bran Flakes, Wheat Cereal. Net Wt 18oz (1 lb 2 oz) 510g. UPC 0 41415-24305 7. D
Recalled by Post Consumer Brands, LLC
Foreign Material (plastic)
Apr 14, 2026
H-0756-2026
Banana Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazza's Fine
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Yellow #5
Apr 14, 2026
H-0745-2026
Loard's Peppermint Ice Cream - 32 oz; 56 oz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Milk, Soy, Red #40.
Apr 14, 2026
H-0724-2026
Loard's Champagne Sherbert - 32 oz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Milk, Red #40.
Apr 14, 2026
H-0760-2026
Chocolate Showers Ice Cream - 32 oz (5 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Pia
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Soy (with mitigating circumstances)
Apr 14, 2026
H-0737-2026
Loard's Lime Sherbert - 32 oz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Milk, Wheat, Soy, Yellow #5, Green #3.
Apr 14, 2026
H-0719-2026
Loard's Brownie Nut Fudge Ice Cream - 32 oz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Milk, Walnuts, Eggs, Wheat, Soy.
Apr 14, 2026
H-0757-2026
Burgundy Cherry Ice Cream - 32 oz (4 labels: Mollie Stone's; Dehoff's; Farmer Joe's, Piazz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Red #40, Blue #1, Blue #2
Apr 14, 2026
H-0736-2026
Loard's Lemon Chiffon Ice Cream - 32 oz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Milk, Eggs, Yellow #5.
Apr 14, 2026
H-0754-2026
Loard's Ube Ice Cream - 32 oz
Recalled by Silver Moon LP dba Loard's Ice Cream
Undeclared Milk, Red #3, Red #40, Blue #1, Blue #2.
💊 Drug Recalls
Apr 28, 2026
D-0514-2026
Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b)
Recalled by Ajanta Pharma Ltd.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12
Apr 28, 2026
D-0516-2026
Duloxetine Delayed-Release Capsules, 20 mg, Rx Only, 60 capsules, Marketed by: Ajanta Phar
Recalled by Ajanta Pharma Ltd.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12
Apr 28, 2026
D-0515-2026
Duloxetine Delayed-Release Capsules, 60 mg, Rx Only, 30 capsules, Marketed by: Ajanta Phar
Recalled by Ajanta Pharma Ltd.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12
Apr 27, 2026
D-0540-2026
Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethl
Recalled by B BRAUN MEDICAL INC
Presence of Particulate Matter.
Apr 26, 2026
D-0525-2026
Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Ma
Recalled by Oasis Medical, Inc.
Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations
Apr 26, 2026
D-0547-2026
Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx On
Recalled by Ascend Laboratories, LLC
Failed Dissolution Specifications
Apr 23, 2026
D-0519-2026
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Sin
Recalled by Teva Pharmaceuticals USA, Inc
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration
Apr 22, 2026
D-0501-2026
Similasan, iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made i
Recalled by Thea Pharma, Inc.
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspect
Apr 22, 2026
D-0500-2026
iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, D
Recalled by Thea Pharma, Inc.
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspect
Apr 22, 2026
D-0520-2026
Enalapril Maleate Tablets, USP, 20 mg, 1,000-count bottle, Rx only, Manufactured by: Uniqu
Recalled by JB Chemicals and Pharmaceuticals Ltd
Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities Test
Apr 21, 2026
D-0518-2026
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5%
Recalled by CareFusion 213, LLC
Lack of assurance of Sterility: potential product contamination
Apr 21, 2026
D-0517-2026
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5%
Recalled by CareFusion 213, LLC
Lack of assurance of Sterility: potential product contamination
Apr 20, 2026
D-0492-2026
GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laborat
Recalled by Alcon Research LLC
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
Apr 20, 2026
D-0522-2026
Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pha
Recalled by Breckenridge Pharmaceutical, Inc.
CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
Apr 20, 2026
D-0491-2026
Systane, Lubricant Eye Gel, Night Gel, Sterile, 10g (0.35 oz), Processed in France for: Al
Recalled by Alcon Research LLC
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
Apr 19, 2026
D-0523-2026
NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed
Recalled by Acella Pharmaceuticals, LLC
Chemical contamination; presence of lead and lithium above specification
Apr 19, 2026
D-0499-2026
Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufacture
Recalled by SCOPE HEALTH
Lack of Assurance of Sterility
Apr 16, 2026
D-0489-2026
FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN US
Recalled by Harrow Eye LLC
Lack of Assurance of Sterility
Apr 15, 2026
D-0494-2026
Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous
Recalled by American Regent, Inc.
Labeling: Missing Label
Apr 13, 2026
D-0490-2026
Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premie
Recalled by Premier Dental Products Co
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 inst
🩺 Medical Device Recalls
Apr 21, 2026
Z-2067-2026
BioFire Joint Infection (JI) Panel REF: RFIT-ASY-0138, 30 test Kit.
Recalled by BioFire Diagnostics, LLC
Contamination to in-vitro diagnostic test may result in false positives.
Apr 13, 2026
Z-1966-2026
Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1968-2026
Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (RE
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1958-2026
Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-2164-2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM wa
Recalled by Dexcom, Inc.
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing es
Apr 13, 2026
Z-1955-2026
Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 7821
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-2163-2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iO
Recalled by Dexcom, Inc.
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing es
Apr 13, 2026
Z-1960-2026
Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1951-2026
Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1957-2026
Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1963-2026
Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1959-2026
Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1952-2026
Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF):
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1956-2026
Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1964-2026
Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Mode
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-2165-2026
Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iO
Recalled by Dexcom, Inc.
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing es
Apr 13, 2026
Z-1953-2026
Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1954-2026
Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 7821
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1962-2026
Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
Apr 13, 2026
Z-1969-2026
Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.
Recalled by Philips North America
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination
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