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
Jun 17, 2026
H-1129-2026
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 o
Recalled by MARS SNACKING
Potential contamination with plastic material
Jun 17, 2026
H-1135-2026
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Visi
Recalled by Provision Health Corp. dba PH Labs
Dietary supplement product Vista MAX contains undeclared Yellow#5.
Jun 17, 2026
H-1134-2026
Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Se
Recalled by Provision Health Corp. dba PH Labs
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Jun 17, 2026
H-1130-2026
MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage Patties, N
Recalled by MARS SNACKING
Potential contamination with plastic material
Jun 14, 2026
H-1125-2026
FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DA
Recalled by Western Mixers Produce & Nuts, Inc.
Undeclared peanuts.
Jun 12, 2026
H-1137-2026
a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0
Recalled by NARA ORGANICS INC
Product may be contaminated with Clostridium botulinum.
Jun 9, 2026
H-1136-2026
Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 60
Recalled by Fry Pie Factory LLC
Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)
Jun 9, 2026
N/A
Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH
Recalled by Wells Enterprises, Inc.
Elevated coliforms
Jun 8, 2026
H-0950-2026
Al Yaman Halawa Extra Pistachio 907g (31.994 oz) plastic jars, UPC 5 287000 098083, 12 ret
Recalled by GREENWORLD FOOD EXPRESS (USA) LLC
Product may be contaminated with Salmonella
Jun 2, 2026
H-0938-2026
MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein,
Recalled by Mothers' Milk Bank of Louisiana at Ochsner Baptist
Potential physical contamination: dark spot was noticed on the bottom of container.
Jun 1, 2026
H-1080-2026
Dried Herring Fish 7 oz.
Recalled by Prime Food Processing LLC.
Improperly eviscerated which may result in Clostridium botulinum contamination
May 28, 2026
H-1095-2026
Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC
Recalled by Champion Foods, LLC
potential salmonella contamination
May 27, 2026
H-1075-2026
azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF J
Recalled by Azuma Foods International Inc USA
Undeclared fish.
May 26, 2026
H-1111-2026
Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhe
Recalled by Produce Innovations
Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub san
May 23, 2026
H-1128-2026
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE,
Recalled by MOGO Moringa LLC
Product may be contaminated with Salmonella Typhimurium
May 21, 2026
H-1133-2026
boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g
Recalled by Boichik Bagels, Inc.
Undeclared allergen, sesame.
May 21, 2026
H-0942-2026
1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Docto
Recalled by Total Nutrition Inc
Product may be contaminated with Salmonella.
May 21, 2026
H-1131-2026
boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, wa
Recalled by Boichik Bagels, Inc.
Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
May 21, 2026
H-0948-2026
001165: Standard Pasteurized Donor Human Milk; 100 mL bottles 001198: Pediatric Pasteurize
Recalled by University of California Health Milk Bank
Product is potentially contaminated with foreign material (plastic particles).
May 21, 2026
H-1132-2026
boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, who
Recalled by Boichik Bagels, Inc.
Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.
May 20, 2026
H-1110-2026
El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard b
Recalled by Alb-USA Enterprises Inc
Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
May 20, 2026
H-0951-2026
Fairhope Roasting Company Cold Brew Coffee Concentrate, packaged in 1-gallon plastic jugs,
Recalled by Fairhope Roasting Company
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement
May 19, 2026
H-0903-2026
Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per
Recalled by Hometown Food Company
Undeclared egg
May 18, 2026
H-0913-2026
ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64
Recalled by Refresqueria Estrella Inc.
Undeclared FD&C Red 40
May 18, 2026
H-0912-2026
Farm Rich Pizza Cheese Crunchers
Recalled by Rich Products Corp
May contain metal pieces
💊 Drug Recalls
Jun 28, 2026
D-0661-2026
Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured by: Cipla
Recalled by Cipla USA, Inc.
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Jun 28, 2026
D-0676-2026
Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured by: Cipla
Recalled by Cipla USA, Inc.
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Jun 28, 2026
D-0675-2026
Cinacalcet Hydrochloride Tablets, 60 mg, 30-count bottle, Rx Only, Manufactured by: Cipla
Recalled by Cipla USA, Inc.
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
Jun 25, 2026
D-0660-2026
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate
Recalled by Lannett Company Inc.
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
Jun 22, 2026
N/A
Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Dilu
Recalled by Lupin Pharmaceuticals Inc.
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing
Jun 21, 2026
D-0617-2026
DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60), 60 Caps
Recalled by Direct Rx
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Jun 16, 2026
D-0628-2026
Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries
Recalled by SUN PHARMACEUTICAL INDUSTRIES INC
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablet
Jun 15, 2026
D-0609-2026
Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), R
Recalled by The Harvard Drug Group LLC
Subpotent Drug
Jun 11, 2026
D-0657-2026
Synjardy XR Tablets (empagliflozin and metformin hydrochloride extended-release tablets),
Recalled by Boehringer Ingelheim Pharmaceuticals, Inc.
CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper
Jun 11, 2026
D-0596-2026
Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx O
Recalled by Par Health USA, LLC
Crystallization; identified as Buprenorphine free base
Jun 10, 2026
D-0643-2026
BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0646-2026
ChloraPrep FREPP, Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcoh
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0652-2026
BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol)
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0651-2026
BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol),
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0650-2026
BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alco
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0644-2026
BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0647-2026
BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0649-2026
BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alco
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0648-2026
BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
Jun 10, 2026
D-0645-2026
BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG), and 70% v/v isopropyl alcohol
Recalled by CareFusion 213, LLC
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and steri
🩺 Medical Device Recalls
Jun 15, 2026
Z-2644-2026
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer;
Recalled by Accuray Incorporated
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operat
Jun 15, 2026
Z-2640-2026
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer;
Recalled by Accuray Incorporated
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operat
Jun 8, 2026
Z-2674-2026
Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Sing
Recalled by Zimmer Surgical Inc
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection.
Jun 8, 2026
Z-2673-2026
Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual
Recalled by Zimmer Surgical Inc
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection.
Jun 7, 2026
Z-2648-2026
ARTIS icono ceiling. Model Number: 11328100.
Recalled by Siemens Medical Solutions USA, Inc
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws
Jun 4, 2026
Z-2645-2026
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Numb
Recalled by Medela Inc
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue
Jun 4, 2026
Z-2579-2026
Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following syste
Recalled by Philips North America Llc
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the eq
Jun 3, 2026
Z-2654-2026
MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461
Recalled by BD SWITZERLAND SARL
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
Jun 2, 2026
Z-2623-2026
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Recalled by Remel, Inc
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
May 31, 2026
Z-2649-2026
Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
Recalled by Carl Zeiss Meditec AG
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
May 28, 2026
Z-2463-2026
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1,
Recalled by Hamilton Medical AG
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectab
May 27, 2026
Z-2609-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2607-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ9
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2611-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ9090
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2608-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ARTERIAL L
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2612-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2613-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS CDS98226
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2606-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2610-2026
Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA - ROOM S
Recalled by Medline Industries, LP
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involvi
May 27, 2026
Z-2532-2026
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Scr
Recalled by Acumed LLC
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.
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Subscribe at FDA.gov ↗What you can do
- Check the official FDA recall search at fda.gov/safety/recalls for the most current list.
- If you have a recalled product: stop using it, photograph the package + lot number for your records, and follow the return/refund instructions on the FDA enforcement record.
- For prescription drug recalls: do not stop a medication on your own — call your doctor or pharmacist first. They may swap to a different manufacturer's version of the same drug.
- For Class I food recalls: throw out the product. Don't donate it. Wipe down shelves and surfaces that touched it.
- Also check non-FDA recalls: USDA meat/poultry and CPSC consumer products (toys, appliances, etc.).
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