Michigan recalls
3,531 federal recalls affecting Michigan in the last 12 months - 169 Michigan-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-08CPSCPNW ComponentsNationwideStop using PNW Components Loam Pedal Gen 2
The axle on PNW Components Loam Pedal Gen 2 mountain bike pedals can crack and cause the pedal to detach from your bike while riding, creating a fall risk. The company has received four reports of this problem, though no injuries have been reported yet.
- 2026-01-08CPSCPress Play ProductsNationwideStop using Isla Rae wireless chargers
Isla Rae magnetic wireless chargers can overheat and explode during use, creating a fire and burn risk. About 13,200 units were sold at T.J. Maxx and Marshalls stores between June 2024 and November 2025. No injuries have been reported so far.
- 2026-01-08CPSCNationwideStop using Kori Gey Water Elf Kit light
Kori Gey Water Elf craft toy kits sold on Amazon contain a LED light with a button cell battery that children can easily access and open. Swallowed button batteries can cause serious internal injuries, chemical burns, and death.
- 2026-01-08CPSCRHNationwideContact RH about your antler chandelier
RH antler chandeliers (48" and 60" sizes) can fall from vaulted or sloped ceilings if the mounting hardware breaks. This happens when the chandelier is installed at an angle rather than level. RH has received four reports of chandeliers detaching, though no injuries have been reported yet.
- 2026-01-08CPSCindriverNationwideStop using Lterfear pounding toys immediately
The Lterfear Multifunction Pounding Game (model D888) contains high-powered magnets that can detach and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious internal injuries including intestinal perforation, blockage, and potentially death.
- 2026-01-08CPSCYolaahNationwideStop using Yolaah bed rails model BR-01
Yolaah bed rails (model BR-01) 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 14,250 units were sold online through Amazon between September and October 2025.
- 2026-01-08CPSCVasicarNationwideStop using Vasicar 18-drawer dressers immediately
Vasicar 18-drawer dressers can tip over and trap children if not securely anchored to a wall. These dressers do not meet federal safety standards for furniture stability. About 4,155 units were sold online between September and November 2025.
- 2026-01-08CPSCSangoheNationwideStop using Sangohe bed rails immediately
Sangohe 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 26,200 units sold online at Amazon and Walmart between August 2023 and October 2025 are affected.
- 2026-01-08CPSCShiahahaNationwideStop using Rattan 6-Drawer Dresser if not wall-anchored
Rattan 6-Drawer Dressers (model YD001) sold on Amazon can tip over and trap children if they are not securely anchored to a wall. The dressers do not meet federal safety standards for furniture stability. About 870 units were sold between September and November 2025.
- 2026-01-08CPSCNFSVLBNationwideStop using NFSVLB baby bath seats
NFSVLB baby bath seats (model ZY2025) can tip over during use and have openings that allow infants to slip down and become trapped underwater. The seats do not meet safety standards for infant bath products. About 1,430 seats were sold on Amazon between May and October 2025.
- 2026-01-08CPSCMarcus AdlerNationwideStop using Julie and Judah pajamas and shorts
Marcus Adler Glove Co. is recalling Julie and Judah brand pajama pants and shorts because they don't meet federal flammability standards for children's sleepwear. These garments could catch fire more easily than safe sleepwear, risking burn injuries to children.
- 2026-01-08CPSCKalencomNationwideStop using SARO Braided Crib Bumpers immediately
Kalencom recalled SARO Braided Crib Bumpers (Model 1374) because they violate the federal ban on crib bumpers and can block an infant's breathing, creating a suffocation risk. The bumpers were sold in salmon, gray, and mint colors at MacroBaby, Kalencombaby.com, and Target.com from May 2024 through October 2025. No injuries have been reported.
- 2026-01-08CPSCBabyBondNationwideStop using BabyBond retractable safety gates
BabyBond retractable safety gates can allow a child's torso to fit through the gap between the gate and floor, creating a serious entrapment risk. The gates were sold at Target.com between November 2024 and October 2025. No injuries have been reported, but the hazard poses a risk of serious injury or death.
- 2026-01-08CPSCGeneracNationwideStop using your DR Power leaf vacuum
Pieces inside DR Power leaf vacuums can come loose or debris can pierce the chute, causing material to shoot out and potentially cut users or bystanders. The company has received 46 reports of debris being ejected, though no injuries have been reported yet.
- 2026-01-08CPSCLeboNationwideStop using Agrish adult bed rails immediately
Agrish adult portable bed rails (models 2512, 2513, and 2516) can trap users between the rail and mattress, creating a serious risk of entrapment and suffocation. The rails do not meet federal safety standards. About 5,000 units were sold on Amazon between April and October 2025.
- 2026-01-07FDA-DeviceBeaver-VisitecClass IINationwideCheck BVI Leos system USB cable for defect
Beaver-Visitec International's BVI Leos Laser and Endoscopy System (Model OME6000U) has a manufacturing defect in the USB cable that connects the Nurse Monitor touchscreen to the System Controller. The cable is missing required ferrite components that protect against electromagnetic interference. Five units with specific serial numbers were affected and distributed in Florida, Michigan, Oklahoma, Texas, and Wisconsin.
- 2026-01-07FDA-DevicePhilipsClass IINationwideStop using affected Philips EPIQ ultrasound systems
Philips EPIQ Ultrasound Systems with the X5-1c transducer and certain software versions may unexpectedly restart on their own. This automatic reboot can damage the transducer. No injuries have been reported.
- 2026-01-07FDA-DeviceSheathing TechnologiesClass IINationwideStop using Sheathes3D probe covers
Sheathes3D Seamless Viral Barrier ultrasound probe covers may have manufacturing defects that could allow contamination during medical use. This poses a risk of infection to patients. The recall affects a limited quantity distributed in Washington State.
- 2026-01-07FDA-DeviceFerndaleClass IINationwideStop using Mastisol Liquid Adhesive lot 24161B
Ferndale Laboratories is recalling Mastisol Liquid Adhesive (lot 24161B, expiration 10-31-2029) because the butyrate tube can crack when you try to use it, making the product unusable. This affects 24,589 vials distributed in the US and UK.
- 2026-01-07FDA-DeviceVortex SurgicalClass IINationwideStop using Vortex Surgical laser probe (lot 2509040)
Some units of the Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe (catalog VS0135.25, lot 2509040) may not fit smoothly through a 25-gauge cannula as intended. This could affect proper use during medical procedures. The recall affects 221 units distributed in the US and Japan.
- 2026-01-07FDA-DeviceAtomstackClass IINationwideStop using Atomstack laser processing equipment
Atomstack material processing laser products lack a required remote interlock connector that is designed to shut down the laser if the protective enclosure is opened. This safety feature is mandated by federal laser safety regulations to prevent accidental exposure.
- 2026-01-07FDA-FoodTom BumbleClass IINationwideStop eating Tom Bumble Nutty candy
Tom Bumble LLC is recalling Nutty Peanut Butter Flake Candy bars because they may contain foreign material. The affected products have Best By dates between May 21, 2026 and June 9, 2026. No injuries have been reported.
- 2026-01-07FDA-DrugZydusClass IIINationwideCheck your trazodone tablets for dents
Zydus Pharmaceuticals is recalling certain bottles of trazodone 100mg tablets because some tablets have dents on the surface. The defect affects lot EA00237A with an expiration date of 04/30/2027. No injuries have been reported.
- 2026-01-07FDA-DrugGlenmarkClass IINationwideStop using Glenmark Ondansetron 4mg tablets
Glenmark Pharmaceuticals discovered that blister packs containing Ondansetron 4mg orally disintegrating tablets are not fully sealed, allowing tablets to fall out. The affected product was repackaged and distributed nationwide. This applies to lot #19251311 with an expiration date of April 2027.
- 2026-01-07FDA-DrugNovo NordiskClass IINationwideStop using Novo Nordisk Wegovy injection pens
Novo Nordisk has recalled specific batches of Wegovy (semaglutide) 1 mg injection pens because hair was found inside prefilled syringes. This affects two lot numbers distributed nationwide. No injuries have been reported.
- 2026-01-07FDA-DrugNovo NordiskClass IINationwideStop using Wegovy 0.5 mg prefilled pens (specific lots)
Novo Nordisk discovered hair in some prefilled Wegovy injection pens. This affects specific lot numbers manufactured in Denmark. No injuries have been reported.
- 2026-01-07FDA-DrugCareFusionClass IINationwideStop using BD ChloraPrep Triple Swabsticks
CareFusion 213, LLC is recalling BD ChloraPrep Triple Swabsticks (a skin antiseptic swab) because the manufacturer cannot confirm the product was properly sterilized. The affected lot (#5086623, expiring 3/31/2028) was distributed nationwide. No injuries have been reported.
- 2025-12-31FDA-DeviceBeckman CoulterClass IINationwideStop using affected Beckman Coulter Bicarbonate Reagent
Beckman Coulter Bicarbonate Reagent (catalog numbers OSR6137, OSR6237, OSR6637) used in laboratory analyzers may produce falsely high bicarbonate test results. This happens because a substance in blood samples called Lactate Dehydrogenase (LDH) interferes with the test. Affected lot numbers are listed in specific ranges for each catalog number.
- 2025-12-31FDA-DeviceMedtronicClass IINationwideUpdate Medtronic Restore Programmer App immediately
A software problem in the Medtronic Restore Clinician Programmer App (versions before v.1.0.4489) can cause a Device Reset message that cannot be cleared. In rare cases, this prevents the pain management device from resuming therapy, causing patients to experience pain symptoms again. The implanted devices themselves are not affected—only the programmer application used by clinicians.
- 2025-12-31FDA-DeviceCookClass IINationwideContact Cook Medical about liver access device
Cook Medical recalled Rösch-Uchida Transjugular Liver Access Sets (part number RUPS-100) used in liver procedures because some units were manufactured incorrectly. Affected devices may have been cut to the wrong length, not properly trimmed, or not inspected. Only 23 units were affected worldwide.
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