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
Aug 17, 2026
H-1265-2026
Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper
Recalled by Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
Aug 17, 2026
H-1266-2026
Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper out
Recalled by Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
Aug 17, 2026
H-1264-2026
Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in pape
Recalled by Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
Aug 17, 2026
H-1268-2026
Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in pa
Recalled by Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
Aug 17, 2026
H-1269-2026
Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 0415
Recalled by Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
Aug 17, 2026
H-1267-2026
Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 041548612041, packaged in paper
Recalled by Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
Aug 13, 2026
H-1245-2026
Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 000
Recalled by Gifford's Dairy, Inc.
Potential foreign object contamination: rubber pieces
Aug 13, 2026
H-1309-2026
THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; N
Recalled by THE HAMPTON GROCER
Product may be contaminated with Salmonella.
Aug 12, 2026
H-1305-2026
Prince ITALIAN BREAD; Sesame; ITALIAN & FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); ING
Recalled by Prince Bakery Inc
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Aug 12, 2026
H-1304-2026
Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOU
Recalled by Prince Bakery Inc
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Aug 12, 2026
H-1307-2026
Prince PAN DE MANTECA; SPANISH STYLE; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEAC
Recalled by Prince Bakery Inc
Milk is not declared in the Contains statement.
Aug 12, 2026
H-1306-2026
Prince Sesame FRENCH BREAD; LONG FRENCH; Net Wt. 10 oz (284g); INGREDIENTS: ENRICHED BLEAC
Recalled by Prince Bakery Inc
Sesame is not declared in the ingredient statement but is declared in the statement of identity.
Aug 11, 2026
H-1244-2026
Product is Potato Sourdough Bread and sold under three following names: Potato Market Loa
Recalled by Grand Central Bakery - Oregon Inc. dba Grand Central Bakery,
Foreign object: May contain metal pieces
Aug 10, 2026
H-1278-2026
Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans
Recalled by Byron White Formulas, Inc.
Label does not declare walnuts in English
Aug 10, 2026
H-1271-2026
Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Chee
Recalled by CUISINE, KETTLE
Product had a presumptive positive test result for Listeria monocytogenes
Aug 10, 2026
H-1277-2026
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans ni
Recalled by Byron White Formulas, Inc.
Label does not declare walnuts in English
Aug 10, 2026
H-1276-2026
Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Ju
Recalled by Byron White Formulas, Inc.
Label does not declare walnuts in English
Aug 9, 2026
H-1243-2026
VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1.58 OZ (45g) UPC 4 335619 355491 DISTRIBUTED BY
Recalled by Lidl US TRADING
Salmonella. The firm received a positive test result of Salmonella in the product.
Aug 9, 2026
H-1332-2026
Mehadrin Chocolate Leben; 6 OZ (170g) CUPS, UPC: 070784023144
Recalled by UPSTATE NIAGARA COOPERATIVE
Product may have been improperly pasteurized.
Aug 6, 2026
H-1249-2026
Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various size
Recalled by WFM Purchasing, LP
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Aug 6, 2026
H-1252-2026
Whole Foods Spicy Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic
Recalled by WFM Purchasing, LP
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Aug 6, 2026
H-1250-2026
Whole Foods Pomegranate Guacamole Dip, Keep Refrigerated. Packed in various sized clear p
Recalled by WFM Purchasing, LP
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Aug 6, 2026
N/A
Food to Live Organic SuperGrass Powder; 6 oz, 12 oz, 1 lb, 4 lb
Recalled by Lexunder Inc
Contaminated with Salmonella
Aug 6, 2026
H-1247-2026
Whole Foods Mild Guacamole Dip No Tomatoes, Keep Refrigerated. Packed in various sized cl
Recalled by WFM Purchasing, LP
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
Aug 6, 2026
H-1333-2026
Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT (Item 136990, UPC 742365002700) and 18 CT
Recalled by Horizon Organic Dairy, LLC
Product has the potential to be spoiled.
💊 Drug Recalls
Aug 30, 2026
D-0833-2026
Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufact
Recalled by Supernus Pharmaceuticals, Inc.
Failed dissolution specifications.
Aug 25, 2026
D-0830-2026
Carton label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, 4 Single Dos
Recalled by Mylan Pharmaceuticals Inc
Failed Dissolution Specifications
Aug 23, 2026
D-0831-2026
Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Ca
Recalled by Hikma Pharmaceuticals USA INC.
Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).
Aug 23, 2026
D-0834-2026
traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia
Recalled by Teva Pharmaceuticals USA, Inc
Presence of Foreign Tablets/Capsules
Aug 20, 2026
D-0828-2026
Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg
Recalled by Lexia LLC
CGMP Deviations: Potential contamination of raw material
Aug 20, 2026
D-0829-2026
Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 30
Recalled by Lexia LLC
CGMP Deviations: Potential contamination of raw material
Aug 20, 2026
N/A
Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporat
Recalled by Golden State Medical Supply Inc.
Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissoluti
Aug 13, 2026
D-0824-2026
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Oc
Recalled by Allies Group Inc.
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on
Aug 13, 2026
D-0826-2026
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Oc
Recalled by Allies Group Inc.
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on
Aug 13, 2026
D-0823-2026
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Oc
Recalled by Allies Group Inc.
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on
Aug 13, 2026
D-0825-2026
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Oc
Recalled by Allies Group Inc.
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on
Aug 12, 2026
D-0804-2026
Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufact
Recalled by Apotex Corp.
Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria
Aug 11, 2026
D-0832-2026
Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical
Recalled by B BRAUN MEDICAL INC
Presence of Particulate matter.
Aug 9, 2026
D-0790-2026
Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Us
Recalled by Church & Dwight Co., Inc.
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
Aug 9, 2026
D-0827-2026
Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufac
Recalled by Fresenius Kabi USA, LLC
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
Aug 6, 2026
D-0771-2026
Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b)
Recalled by Golden State Medical Supply Inc.
CGMP deviations: tablets with black specks.
Aug 6, 2026
D-0822-2026
Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg, 100-count bot
Recalled by Bionpharma Inc.
Presence of Foreign Tablets/Capsules
Aug 5, 2026
D-0815-2026
Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Sing
Recalled by Baxter Healthcare Corporation
CGMP Deviations
Aug 5, 2026
D-0785-2026
Levothyroxine Sodium Tablets, USP, 200 mcg (0.2 mg), packaged in a) 90-count bottles (NDC
Recalled by ACCORD HEALTHCARE, INC.
Subpotent Drug
Aug 5, 2026
D-0811-2026
Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL
Recalled by Baxter Healthcare Corporation
CGMP Deviations
🩺 Medical Device Recalls
Aug 17, 2026
Z-3035-2026
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action.
Recalled by Olympus Corporation of the Americas
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.
Aug 10, 2026
Z-3065-2026
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Recalled by Baxter Healthcare Corporation
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is re
Aug 10, 2026
Z-3066-2026
Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
Recalled by Baxter Healthcare Corporation
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is re
Aug 9, 2026
Z-3087-2026
5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
Recalled by Fresenius Medical Care Renal Therapies Group, LLC
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segme
Aug 9, 2026
Z-3084-2026
5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
Recalled by Fresenius Medical Care Renal Therapies Group, LLC
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segme
Aug 9, 2026
Z-3085-2026
5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
Recalled by Fresenius Medical Care Renal Therapies Group, LLC
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segme
Aug 9, 2026
Z-3086-2026
5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
Recalled by Fresenius Medical Care Renal Therapies Group, LLC
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segme
Aug 6, 2026
Z-3043-2026
Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64
Recalled by Philips North America Llc
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems
Aug 6, 2026
Z-3042-2026
Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327, Ingenuity CT China 72
Recalled by Philips North America Llc
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems
Aug 6, 2026
Z-3041-2026
Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332, IQon Spectral CT 7283
Recalled by Philips North America Llc
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems
Aug 6, 2026
Z-3040-2026
Philips Brilliance. Models: Brilliance iCT, Brilliance iCT Upgrades, Brilliance iCT SP. So
Recalled by Philips North America Llc
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems
Aug 5, 2026
Z-3033-2026
ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned,
Recalled by IMRIS Imaging Inc
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the syste
Aug 5, 2026
Z-3034-2026
ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000
Recalled by IMRIS Imaging Inc
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the syste
Aug 5, 2026
Z-3081-2026
LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS
Recalled by Boston Scientific Corporation
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertab
Aug 5, 2026
Z-3083-2026
LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS
Recalled by Boston Scientific Corporation
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertab
Aug 5, 2026
Z-3082-2026
LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS
Recalled by Boston Scientific Corporation
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertab
Aug 3, 2026
Z-3014-2026
Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiograph
Recalled by Canon Medical System, USA, INC.
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional sys
Aug 3, 2026
Z-3089-2026
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number:
Recalled by B Braun Medical Inc
Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label
Jul 30, 2026
Z-3064-2026
HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN)
Recalled by Johnson & Johnson Surgical Vision, Inc.
Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including
Jul 29, 2026
Z-2872-2026
BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered D
Recalled by Bard Access Systems, Inc.
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in e
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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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