Michigan recalls
3691 federal recalls on file affecting Michigan - 616 Michigan-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical devices
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat 5mm instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat devices
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceMedicaClass IINationwideStop using Medica capillary tubes
A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes.
- 2026-02-25FDA-DeviceImmunotechClass IINationwideStop using Immunotech Estrone RIA kits
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.
- 2026-02-25FDA-DeviceBardClass IINationwideStop using affected Bard Broviac and Hickman catheters
Due to damage to outer tray that can potentially compromise the sterile barrier
- 2026-02-25FDA-DeviceMedlineClass IINationwideStop using Medline IV administration sets
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may result in a delay in patient treatment, blood loss, infection, an air embolism, and/or underdosage of medication.
- 2026-02-25FDA-DeviceIntegra LifeSciencesClass IINationwideStop using CVS wound care gel model CVS405406
Potential packaging failures, which could lead to a breach in the sterile barrier.
- 2026-02-25FDA-DeviceIntegra LifeSciencesClass IINationwideStop using affected MEDIHONEY calcium alginate dressings
Potential packaging failures, which could lead to a breach in the sterile barrier.
- 2026-02-25FDA-DeviceIntegra LifeSciencesClass IINationwideStop using Integra MediHoney Gel dressing
Potential packaging failures, which could lead to a breach in the sterile barrier.
- 2026-02-25FDA-DeviceOlympusClass INationwideContact Olympus about UHI-3 insufflation unit recall
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-DeviceOlympusClass INationwideStop using Olympus UHI-2 insufflation units
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-DeviceOlympusClass INationwideStop using Olympus insufflation unit Model UHI
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-FoodWhy Not NaturalClass INationwideStop using Why Not Natural Moringa Capsules
Potential to be contaminated with Salmonella
- 2026-02-24CPSCYiruikeji2024NationwideStop using Yiruikeji2024 magnetic chess games
The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- 2026-02-22USDAClass INationwideThrow out Bremer frozen meatballs
Product Contamination
- 2026-02-19CPSCSamit OutdoorNationwideStop using SAMIT youth helmets immediately
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- 2026-02-19CPSCPrismatic 3D PrintsNationwideStop using Prismatic 3D Prints Book Nooks immediately
The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium coin battery that can be easily accessed by children. In addition, the spare coin battery is not in child resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-02-19CPSCMeijerReturn Meijer children's sleepwear to store
The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children.
- 2026-02-19CPSCJJGooNationwideStop using JJGoo LED balloon lights
The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-02-19CPSCJoly'sNationwideStop using Joly's 80% Vinegar immediately
The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance lacks required warning labels and first-aid treatment instructions. This poses a deadly risk of poisoning if the contents are swallowed and a serious injury from chemical burns to the skin and eyes if improperly handled.
- 2026-02-19CPSCHuakerNationwideStop using Huaker magnetic ball sets immediately
The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.
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