State

Michigan product recalls

72,933 recalls have nationwide distribution and so reach Michigan. 9,517 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total: 9,517
Critical: 1,556
Severe: 2,144
Most recent: 2026-09-09

Of the 9,517 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 2,144 (23%) are Severe.

Which agencies issued them

These figures cover only the 9,517 recalls whose distribution notice names Michigan specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2601–2625 of 82450

HighFDA (Devices)·Z-1655-2026·2026-04-08
Paradise renal denervation catheter distributed despite being marked for scrapping
Recor Medical is recalling one lot of the Paradise Ultrasound Renal Denervation System Catheter because a nonconforming product that should have been scrapped was distributed instead.
Product
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1698-2026·2026-04-08
da Vinci mega needle driver recalled over broken or frayed cables
Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1742-2026·2026-04-08
MiniMed 770G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 770G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1744-2026·2026-04-08
MiniMed 700G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 700G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1757-2026·2026-04-08
Burlington Medical wrap aprons may lose radiation attenuation over time
Burlington Medical is recalling wrap aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Wrap Aprons.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1709-2026·2026-04-08
Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments
Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1686-2026·2026-04-08
Artoura breast tissue expander infusion set needles may be blunt
Mentor Texas is recalling Artoura Breast Tissue Expanders because the infusion sets may contain a dull or blunt needle tip that may be difficult to advance or may break.
Product
Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1680-2026·2026-04-08
Philips Azurion 5 M20 X-ray may not start from foot switch
Philips is recalling the Azurion 5 M20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1675-2026·2026-04-08
Philips Azurion 7 B12 X-ray may not start from foot switch
Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1688-2026·2026-04-08
Stryker surgical light assembly may not support the ceiling cover weight
Stryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System because the light assembly may not adequately support the weight of the ceiling cover.
Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1670-2026·2026-04-08
Philips Allura Xper FD20/20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/20 OR Table; System Code: 722039;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2026·2026-04-08
da Vinci tenaculum forceps recalled over frayed or broken pitch cables
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1672-2026·2026-04-08
Philips Allura Xper FD20/15 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/15 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/15 OR Table; System Code: 722059;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1697-2026·2026-04-08
da Vinci double fenestrated grasper recalled over broken grip cables
Intuitive Surgical is recalling da Vinci S and Si Double Fenestrated Grasper Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including bl
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1660-2026·2026-04-08
Philips Allura Xper FD10F X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10F because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10F; System Code: 722002;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1681-2026·2026-04-08
CPX 4 SILTEX low height expander infusion needles may be blunt
Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the SILTEX low height range because the infusion sets may contain a dull or blunt needle tip.
Product
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1704-2026·2026-04-08
Finesse BTK angioplasty balloon catheter may not meet burst specifications
The Finesse BTK Multicath injectable angioplasty balloon catheter is being recalled because of the potential for the balloon not to meet burst specifications.
Product
Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 French sheath, 0.014" guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon le
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1669-2026·2026-04-08
Philips Allura Xper FD20/20 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/20; System Code: 722038;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1668-2026·2026-04-08
Philips Allura Xper FD20/10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/10; System Code: 722029;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1667-2026·2026-04-08
Philips Allura Xper FD10 OR Table X-ray may not start reliably
Philips is recalling the Allura Xper FD10 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1662-2026·2026-04-08
Philips Allura Xper FD10/10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1671-2026·2026-04-08
Philips Allura Xper FD20/15 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD20/15 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/15; System Code: 722058;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1699-2026·2026-04-08
da Vinci grasping retractor instruments recalled over broken grip cables
Intuitive Surgical is recalling da Vinci S and Si Grasping Retractor Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1666-2026·2026-04-08
Philips Allura Xper FD20 Biplane OR Table X-ray may not start
Philips is recalling the Allura Xper FD20 Biplane OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1748-2026·2026-04-08
Paradigm insulin pump delivery varies with pump height changes
Medtronic is recalling Paradigm insulin pumps models MMT-712 and MMT-715 because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
Paradigm Insulin Pump (MMT-712, MMT-715)
Category
Medical Device
Distribution
Distributed nationwide