Michigan recalls
3,531 federal recalls affecting Michigan in the last 12 months - 168 Michigan-specific plus 3,363 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-09CPSCSeasonal SpecialtiesNationwideStop using Member's Mark 7' Pre-Lit Twinkling Buck
The wires in this decorative light-up buck can be connected incorrectly at the factory, causing a resistor to overheat. This creates a risk of burns or fire. The company has received five reports of smoke and burning smells.
- 2026-04-09CPSCSCUBAPRONationwideStop using SCUBAPRO Monorail Weight Pocket
The D-ring handle on SCUBAPRO Monorail Weight Pockets can detach during diving. If this happens, you won't be able to remove the weight pocket in an emergency to surface safely, creating a serious drowning risk. The company has received two reports of handles detaching, though no injuries have occurred yet.
- 2026-04-09CPSCMaitysNationwideStop using Maitys magnetic drinkware charms
Maitys magnetic drinkware charms sold on Amazon contain loose magnets that can separate and be swallowed by children. High-powered magnets in the digestive system can attract each other or metal objects, causing serious internal injuries including intestinal perforation, blockage, and potentially death.
- 2026-04-09CPSCSilksNationwideStop using Silks children's loungewear sets
Silks children's loungewear sets (sizes 2T–13/14) do not meet federal flammability standards for sleepwear and pose a burn hazard to children. The two-piece sets include a short-sleeved shirt with matching shorts or pants and were sold online from January 2024 through September 2025.
- 2026-04-09CPSCSnoozNationwideStop using Snooz Breez smart fan immediately
Snooz's Breez 2-in-1 Smart Bedroom fan can overheat and catch fire due to corrosion in the power connector. The company has received six reports of fans overheating and smoking, including one confirmed fire. No injuries have been reported so far.
- 2026-04-09CPSCYunguNationwideStop using Easymake portable bed rails
Easymake adult portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 19,000 units were sold online starting in August 2023.
- 2026-04-09CPSCVitaquestNationwideStop using Vitaquest iron supplements immediately
Vitaquest International is recalling multiple iron-containing dietary supplements sold under brands including Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean, and Sakara. The packaging does not meet federal child-resistant requirements, creating a serious poisoning risk if young children swallow the contents.
- 2026-04-09CPSCBissellNationwideStop using BISSELL Steam Shot OmniReach attachments
BISSELL steam cleaner attachments can unexpectedly detach during use and spray hot water or steam, causing burn injuries. The company has received over 200 reports of attachments detaching, including 161 burn injuries. This affects over 1.7 million units sold between October 2024 and March 2026.
- 2026-04-09CPSCWyboticsNationwideStop using Wybotics robotic pool vacuums
Wybotics robotic pool vacuums (Osprey 700 Max and S1 models) have lithium-ion batteries that can overheat and catch fire during charging or normal use. The company has received 10 reports of overheating or fires, with 9 cases of property damage but no injuries so far. Only specific serial numbers are affected.
- 2026-04-08FDA-PRBlaine LabsNationwideStop using Blaine Labs wound care gel
Blaine Labs is recalling three lot numbers of Revitaderm and Tridergel wound care gel (1 oz. and 3 oz. bottles/tubes) because they may contain Lysinibacillus fusiformis, a bacterium found in the environment. The affected products were distributed to healthcare providers only, not sold in stores. No injuries have been reported so far.
- 2026-04-08FDA-DeviceCardinal HealthClass IINationwideCheck Cardinal Health Monoject Tuberculin Syringes
Cardinal Health Monoject Tuberculin Syringes labeled as 1 mL Luer Lock (Catalog 1180100777) actually contain U-100 Insulin syringes inside the packages. This mislabeling could lead to incorrect dosing if the syringes are used without checking the actual contents. The affected lot numbers are 531164X and 531162X.
- 2026-04-08FDA-DeviceGE HealthcareClass IINationwideCheck your GE SIGNA Premier MRI scanner
GE Healthcare SIGNA Premier whole-body MRI scanners may have steel fittings instead of brass fittings on the magnet rear. During service work while the magnet is powered up, the magnetic field could pull on these steel parts, risking injury to technicians.
- 2026-04-08FDA-DeviceOxoidClass IINationwideStop using Oxoid Microbact 12L Kit lot 4494873
Oxoid's Microbact 12L Kit (lot 4494873) may produce ambiguous color reactions in test wells that could lead to incorrect organism identification. This affects a limited number of kits distributed in Georgia and California.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical Kilt Blockers
Burlington Medical Kilt Blockers with Xenolite 800 attenuation material made between January 2025 and January 2026 may degrade over time, reducing how long they work effectively. This affects 94 units across multiple model sizes distributed worldwide.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical Blockers serial number
Burlington Medical has recalled certain Blocker models because the Xenolite 800 material used in their construction may degrade over time, reducing how long the device will work properly. The recall affects units manufactured between January 16, 2025 and January 21, 2026. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical apron serial number
Burlington Medical Demi Half Aprons made with Xenolite 800 material between January 2025 and January 2026 may degrade over time, reducing how long they last. This affects 29 units sold worldwide. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck Burlington Medical half aprons for material degradation
Burlington Medical half aprons manufactured between January 2025 and January 2026 with Xenolite 800 shielding material may degrade over time, reducing their protective effectiveness. This affects 30 different model numbers distributed worldwide. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical leg wraps
Burlington Medical leg wraps manufactured between January 2025 and January 2026 may experience material degradation over time, which could reduce how long the wraps last and their effectiveness. The issue affects specific models that used Xenolite 800 attenuation material. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck Burlington Medical caps for degradation
Burlington Medical issued a recall for certain radiation protection caps (models R8CAP, S8CAP, and U8CAP) manufactured between January 16, 2025 and January 21, 2026. The caps contain attenuation material that may degrade over time, which could reduce their ability to protect against radiation exposure.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck Burlington Medical protective sleeves
Burlington Medical protective sleeves made with Xenolite 800 material may degrade over time, reducing how long they last. This affects sleeves manufactured between January 16, 2025 and January 21, 2026. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideStop using Burlington Medical BAT aprons
Burlington Medical BAT (Breast, Axilla and Thyroid) radiation protective aprons made with Xenolite 800 material between January 2025 and January 2026 may lose their protective effectiveness over time. The material can degrade, reducing how well the apron shields against radiation.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideStop using Burlington Medical wrap aprons
Burlington Medical wrap aprons manufactured between January 16, 2025 and January 21, 2026 contain radiation-shielding material that degrades over time, reducing their protective effectiveness. This affects multiple model numbers across different sizes. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical frontal apron
Burlington Medical is recalling certain frontal aprons (radiation protection garments) with Xenolite 800 shielding material made between January 2025 and January 2026. The material may degrade over time, reducing its ability to protect against radiation exposure. No injuries have been reported.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical Kilt model
Burlington Medical is recalling certain Kilt models because the Xenolite 800 attenuation material used in them may break down over time, reducing how long the product lasts. The recall affects units made between January 16, 2025 and January 21, 2026.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck Burlington Medical vest serial number
Burlington Medical protective vests made with Xenolite 800 attenuation material between January 16, 2025 and January 21, 2026 may weaken over time, reducing their protective lifespan. No injuries have been reported. The company is notifying users and working on a remedy.
- 2026-04-08FDA-DeviceBurlington MedicalClass IINationwideCheck your Burlington Medical Thyroid Shield
Burlington Medical thyroid shields manufactured between January 16, 2025 and January 21, 2026 contain attenuation material that may degrade over time, reducing the shield's protective effectiveness. This affects multiple model numbers and sizes.
- 2026-04-08FDA-DeviceMedtronicClass IINationwideCheck your Medtronic MiniMed insulin pump positioning
Medtronic MiniMed insulin pumps (Paradigm, 600, and 700 series) can deliver too much or too little insulin when the pump is held higher or lower than the infusion site on your body. This happens because gravity affects the pressure inside the pump tubing. Incorrect insulin doses can cause serious blood sugar problems.
- 2026-04-08FDA-DeviceMedtronicClass IINationwideStop using affected Medtronic MiniMed insulin pumps
Medtronic MiniMed insulin pumps (including Paradigm, 600, and 700 series models) may deliver too much or too little insulin when the pump is positioned above or below the infusion site. This happens because gravity affects how insulin flows through the tubing. Too much insulin can cause dangerously low blood sugar; too little can cause dangerously high blood sugar.
- 2026-04-08FDA-DeviceMedtronicClass IINationwideCheck your Medtronic MiniMed insulin pump position
Medtronic MiniMed insulin pumps (Paradigm, 600, and 700 series) can deliver too much or too little insulin depending on whether the pump is held above or below the infusion site. Too much insulin can cause dangerously low blood sugar; too little can cause dangerously high blood sugar and other serious complications.
- 2026-04-08FDA-DeviceMedtronicClass IINationwideStop using Medtronic MiniMed Paradigm insulin pump
Medtronic MiniMed insulin pumps (Paradigm, 600, and 700 series) can deliver too much or too little insulin when the pump is held at different heights relative to the infusion site. Too much insulin can cause dangerously low blood sugar; too little can cause dangerously high blood sugar and serious complications.
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