State

Michigan product recalls

72,986 recalls have nationwide distribution and so reach Michigan. 9,518 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total: 9,518
Critical: 1,556
Severe: 2,145
Most recent: 2026-09-16

Of the 9,518 recalls naming Michigan we have scored against our rubric, 1,556 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,145 (23%) are Severe.

Which agencies issued them

These figures cover only the 9,518 recalls whose distribution notice names Michigan specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6476–6500 of 82504

HighFDA (Devices)·Z-2010-2025·2025-07-02
Altivate Reverse Torx Peripheral Screws Package Labeling Mismatch
Encore Medical is recalling Altivate Reverse Torx Peripheral screws because the package labeling lists a different screw size than what is actually included in the package.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 18mm Model/Catalog Number: 506-04-118 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2005-2025·2025-07-02
BD Insyte Autoguard Shielded IV Catheter needle retraction malfunction
Becton Dickinson is recalling a specific lot of BD Insyte Autoguard Shielded IV Catheters due to reports that the catheter needle may be slow to retract or fail to retract.
Product
REF: 382544 BD Insyte Autoguard Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2006-2025·2025-07-02
BD Insyte Autoguard Winged Shielded IV Catheter Needle Retraction Issue
Becton Dickinson is recalling BD Insyte Autoguard Winged Shielded IV Catheters (Lot# 4282308) because the catheter needle may be slow to retract or fail to retract entirely following use.
Product
REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V409000·2025-07-02
Polestar 2 May Lose Brake Function While Using One Pedal Drive
Certain 2021 and 2024 Polestar 2 vehicles may lose brake function while coasting downhill and using One Pedal Drive mode. Polestar will provide a free over-the-air software update to fix the control module defect.
Product
POLESTAR — POLESTAR POLESTAR 2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2001-2025·2025-07-02
BD Insyte Autoguard Winged IV Catheter needle retraction failure recall
Becton Dickinson is recalling BD Insyte Autoguard Winged IV Catheters (Ref. 381533, Lot 4282452) because the catheter needle may be slow to retract or fail to retract entirely.
Product
REF: 381533, BD Insyte Autoguard Winged, Shielded IV Catheter, 20 GA x 1.00 in (1.1 x 25 mm) 65mL/min, STERILEEO,RxOnly
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0059-2025·2025-07-02
Madeline's Patisserie Raspberry Croissants Recalled for Undeclared Wheat
Element 112, LLC is recalling Madeline's Patisserie Raspberry Croissants because they contain undeclared wheat, a major allergen. The recall affects approximately 194 cases distributed to four distributors in Michigan and Ohio.
Product
1) Madeline's Patisserie 2.5 ounce Raspberry Croissant, Net Wt. 4 lbs. (1,814.37 g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case 2) Madeline's Patisserie 3.5 ounce Raspberry Croissant, Net Wt. 6 lbs. 10 oz. (3,005.05 g), packaged in a
Category
Food
Distribution
2 states
ModerateFDA (Food)·H-0091-2025·2025-07-02
Prothin Dietary Supplement Recall for Undeclared Food Dyes
Preventics, Inc. is recalling Prothin dietary supplement packets because they contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules, which may affect consumers with dye sensitivities or allergies.
Product
Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0092-2025·2025-07-02
Super ProTHIN Plus Dietary Supplement Recalled for Undeclared Dyes
Preventics, Inc. dba Legere Pharmaceuticals is recalling Super ProTHIN Plus dietary supplement because gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food colorings.
Product
Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0094-2025·2025-07-02
Probese Caps dietary supplement recalled for undeclared food dyes
Probese Caps, a dietary supplement with Iron sold in 90-count bottles, is being recalled because it contains undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules.
Product
Probese Caps, dietary supplement with Iron. 90-count bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0060-2025·2025-07-02
Madeline's Patisserie Butter Croissant Buns recalled for undeclared wheat
Element 112, LLC is recalling Madeline's Patisserie 4.25 Inch Butter Croissant Buns because they contain undeclared wheat, a major food allergen.
Product
Madeline's Patisserie 4.25 Inch Butter Croissant Bun, Net Wt. 4 lbs. 6 oz (1,984.47 g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case
Category
Food
Distribution
2 states
ModerateFDA (Devices)·Z-2011-2025·2025-07-02
Altivate Reverse Torx Peripheral Screw package labeling mismatch
Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because the package labeling lists a different size than the actual product included inside.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm Model/Catalog Number: 506-04-130 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
ModerateFDA (Food)·H-0088-2025·2025-07-02
Carley's Soft Baked Iced Lemon Cookies recalled for misbranded color
Carley's Inc. is recalling Soft Baked Iced Lemon Cookies because the label incorrectly identifies an artificial yellow color instead of listing it as FD&C Yellow #5 as required.
Product
Carley s Soft Baked Iced Lemon Cookies, 5.34oz Plastic Tray, clear film overwrap w/ Label, 12 units per case
Category
Food
Distribution
15 states
ModerateFDA (Food)·H-0070-2025·2025-07-02
Big O' Smokehouse Whitefish Spread recalled for plastic contamination
Big O' Smokehouse is recalling 4lb and 8oz containers of Whitefish Spread due to white plastic fragments found in the product. The affected spread was distributed to retail stores and distributors in Michigan and Illinois.
Product
Big O' Smokehouse 4lb Whitefish Spread Big O' Smokehouse 8oz Whitefish Spread Packaged in plastic containers
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-0489-2025·2025-07-02
Dobutamine Injection Recall Due to Discoloration and Cracked Vials
Pfizer is recalling one lot of Dobutamine Injection (250 mg/20 mL) nationwide due to discoloration and discolored solution caused by cracked vials. Healthcare facilities should quarantine and return affected units.
Product
DOBUTAMINE — DOBUTAMINE (DOBUTAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0483-2025·2025-07-02
Tirzepatide Injections Pre-filled Syringe Recalled for Sterility Assurance
Thrive Health Solutions is recalling Tirzepatide Injections 20mg/mL pre-filled syringes due to lack of assurance of sterility. Approximately 826 syringes distributed nationwide are affected.
Product
Tirzepatide Injections, 20mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2012-2025·2025-07-02
Caphosol Artificial Saliva sachets recalled for out-of-specification stability
Recordati Rare Diseases is recalling Caphosol Artificial Saliva 32-dose sachets because stability test results for Solution B were out of specification during process validation.
Product
Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 mL sachets aqueous solution (32 sachets Solution A Phosphate, 32 sachets Solution B Calcium)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1995-2025·2025-07-02
Medline Umbilical Tray sterile packaging defect recall
Medline is recalling umbilical trays due to a possible packaging defect in the outer Tyvec pouch that protects the sterile product. The defect may compromise sterility.
Product
Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2009-2025·2025-07-02
Altivate Reverse Torx Peripheral Screw labeling mismatch recall
Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling lists a different size than the actual product included inside.
Product
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm Model/Catalog Number: 506-04-122 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-2026-2025·2025-07-02
Jewel Precision Reusable Rigid Sterilization Container System Instructions Mismatch
Jewel Precision Reusable Rigid Sterilization Container System (Model JP-24-6) is being recalled because the Instructions for Use do not match the FDA-cleared indications for use or sterility shelf life.
Product
Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog Number: JP-24-6.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·H-0093-2025·2025-07-02
Protrim Plus Dietary Supplement Recall for Undeclared Food Dyes
Protrim Plus dietary supplement 90-capsule bottles contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules. The product was distributed nationwide and may pose a risk to consumers with dye sensitivities or allergies.
Product
Protrim Plus, dietary supplement. 90 capsule/bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2027-2025·2025-07-02
Atellica CH Diluent Contaminated with Sodium Hypochlorite
Siemens Healthcare Diagnostics is recalling Atellica CH Diluent (SMN 11099300, Lot 0000195412) due to contamination with sodium hypochlorite, which may affect laboratory test results.
Product
Product: Atellica CH Diluent - CONS 2 x 1.5L; Siemens Material Number (SMN): 11099300;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1998-2025·2025-07-02
LUCAS Chest Compression System demonstration units recalled
Jolife AB is recalling LUCAS 2, 3, and 3.1 chest compression system demonstration units that may have been provided to customers for clinical use instead of demonstration purposes only.
Product
LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Food)·H-0095-2025·2025-07-02
NutriLean Dietary Supplement Contains Undeclared Food Dyes
Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplements nationwide because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes, which are not listed on the label.
Product
NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Food)·H-0096-2025·2025-07-02
Rodex Forte dietary supplement recalled for undeclared food dyes
Rodex Forte dietary supplement (90-capsule bottles) is being recalled because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1), which are not listed on the label.
Product
Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V446000·2025-06-30
TICO Recalls 2024-2025 Pro Spotter Trucks Due to Brake Line Fitting Defect
TICO is recalling 2024-2025 Pro Spotter trucks because a non-DOT brake line fitting may reduce braking performance, increasing crash risk.
Product
TICO — TICO PRO SPOTTER
Category
Vehicle
Distribution
Distributed nationwide