State

Minnesota product recalls

73,806 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,851
Critical: 1,137
Severe: 2,246
Most recent: 2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42076–42100 of 81657

HighFDA (Devices)·Z-2320-2018·2018-07-04
St Jude Medical Recalls Fortify ICDs and CRT-Ds for Security Firmware Update
St Jude Medical is recalling Fortify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access. Older devices may require permanent disabling of RF communication.
Product
Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2287-2018·2018-07-04
Teleflex Universal Shears Recalled Due to Handle Melting During Sterilization
Teleflex Medical Europe Ltd is recalling 573 units of Pilling Universal Shears because incorrect plastic was used for the handles, causing them to melt during sterilization.
Product
Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2317-2018·2018-07-04
Medtronic Model 53401 Pacemakers Recalled for Unexpected Power Reset
Medtronic is recalling 1,108 Model 53401 temporary external pacemakers because they may revert to nominal settings during use due to an unexpected power on reset.
Product
Single Chamber Temporary External Pacemaker, Model 53401
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-2313-2018·2018-07-04
Siemens Artis zee MP Recall for Display Failure After Power Save
Siemens is recalling Artis zee MP systems because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Product
Artis zee MP, Material no. 10094139, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2322-2018·2018-07-04
St Jude Medical Recalls High Voltage Implantable Cardiac Devices for Security Firmware
St Jude Medical is releasing new firmware for high voltage implantable cardiac devices to strengthen security against unauthorized access.
Product
Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2305-2018·2018-07-04
Siemens Artis Q.zen Biplane Recalled for Display Failure
Siemens Medical Solutions is recalling two Artis Q.zen biplane systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation or patient transfer.
Product
Artis Q.zen biplane, Material no. 10848355, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2283-2018·2018-07-04
Siemens ARTIS Pheno X-Ray System Recalled for C-Arm Drop Hazard
Siemens is recalling 39 ARTIS Pheno Interventional Fluoroscopic X-Ray Systems because the C-arm may drop up to 20 mm, potentially injuring patients.
Product
ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2304-2018·2018-07-04
Siemens Artis Q Ceiling Recalled for Display Failure After Power Save
Siemens Medical Solutions is recalling five Artis Q ceiling units because the display may fail to show an image after exiting power save mode, potentially requiring treatment cancellation.
Product
Artis Q ceiling, Material no. 10848281, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2314-2018·2018-07-04
Siemens Artis zeego X-ray System Recalled for Display Failure
Siemens Medical Solutions is recalling 56 Artis zeego systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Product
Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2308-2018·2018-07-04
Siemens Artis zee Biplane Recalled for Display Failure After Power Save
Siemens is recalling 68 Artis zee biplane systems because the large display may remain black after exiting power save mode, potentially requiring treatment cancellation or patient transfer.
Product
Artis zee biplane, Material no. 10094141, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2288-2018·2018-07-04
HLD Systems Washer Pasteurizer Recalled for Terminal Block Overheating
Cenorin, LLC is recalling 14 HLD Systems 600 Series Washer/Pasteurizers because a supplier quality issue with terminal blocks may cause overheating, charring, or burning.
Product
HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model 610HT, 230V Product Usage: Clean and thermally disinfect medical devices using full immersion pasteurization
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2327-2018·2018-07-04
St Jude Medical Recalls Unify Assura ICDs for Security Firmware Update
St Jude Medical is recalling Unify Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Unify Assura, Sterile EO, Model #/ Part #: CD3257-40/100042333, 100059944; CD3257-40Q/100042334, 100059936; CD3261-40/100048460, 100048546, 100059897, 100059954, 100059996, 100078828; CD3261-40Q/100048568, 100048581, 100059898, 100059955, 100059997, 100078853…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2018·2018-07-04
Zimmer Biomet Recalls Vanguard Knee Bearings Due to Packaging Mix-up
Zimmer Biomet is recalling 48 Vanguard Complete Knee System tibial bearings because two lots were commingled, creating a risk that 14mm bearings are packaged in 12mm boxes or vice versa.
Product
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The product is intended for use in knee joint replacement arthroplasties.
Category
Medical Device
Distribution
18 states
HighFDA (Devices)·Z-2325-2018·2018-07-04
St Jude Medical Recalls Quadra Assura MP Implantable Cardiac Devices for Security Update
St Jude Medical is recalling 68,117 Quadra Assura MP implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Quadra Assura MP, Sterile EO, Model #/ Part #: CD3269-40/100043177; CD3269-40Q/100043178; CD3271-40/100043130; CD3271-40Q/100043191; CD3369-40C/100080339, 100080478; CD3369-40Q/100080439, 100080476, 100105528; CD3371-40/100078814, 100079232, 100079513…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2324-2018·2018-07-04
St Jude Medical Recalls Quadra Assura ICDs for Security Firmware Update
St Jude Medical is recalling 72,673 Quadra Assura implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Quadra Assura, Sterile EO, Model #/ Part #: CD3265-40/100042335, 100059846; CD3265-40Q/100042336, 100059847; CD3267-40/100042956, 100043569, 100059961, 100078810; CD3267-40Q/100043132, 100043539, 100059917, 100059956, 100078904; CD3365-40C/100080435, 100080436…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2328-2018·2018-07-04
St Jude Medical Recalls Unify Quadra ICDs for Security Firmware Update
St Jude Medical is recalling Unify Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2018·2018-07-04
Siemens Artis zee floor MN recalled for display failure
Siemens is recalling Artis zee floor MN systems because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Product
Artis zee floor MN, Material no. 10094142, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2290-2018·2018-07-04
RayStation Radiation Therapy Software Recalled for Dose Calculation Accuracy Issues
RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software versions 6.0 through 7.0 because dose calculation accuracy may be less than expected in some situations.
Product
RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2318-2018·2018-07-04
St Jude Medical Recalls Implantable Cardiac Devices for Security Firmware Update
St Jude Medical is recalling implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
Product
Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2311-2018·2018-07-04
Siemens Artis zee floor recall due to display failure
Siemens is recalling 14 Artis zee floor systems because the display may fail to show images after power save mode, potentially requiring treatment cancellation.
Product
Artis zee floor, Material no. 10094135, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2310-2018·2018-07-04
Siemens Artis zee Ceiling Recalled for Display Malfunction
Siemens is recalling 73 Artis zee ceiling units because the display may fail to show images after power save mode, potentially requiring procedure cancellation.
Product
Artis zee ceiling, Material no. 10094137, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2307-2018·2018-07-04
Siemens Artis Q.zen floor recall for display failure after power save
Siemens is recalling Artis Q.zen floor units because the display may fail to show images after power save mode, potentially requiring procedure cancellation or patient transfer.
Product
Artis Q.zen floor, Material no. 10848353, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2306-2018·2018-07-04
Siemens Artis Q.zeego X-ray System Display Malfunction Recall
Siemens is recalling four Artis Q.zeego X-ray systems because the display may remain black after power save mode, preventing normal operation and requiring procedure cancellation or patient transfer.
Product
Artis Q.zeego, Material no. 10848283, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2329-2018·2018-07-04
St Jude Medical Recalls Merlin PCS Programmer Firmware for Security
St Jude Medical is releasing new firmware for Merlin PCS programmers to strengthen security against unauthorized access to cardiac devices.
Product
Merlin PCS programmer (Model # 3650), Software (Model # 3330)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2303-2018·2018-07-04
Siemens Artis Q Biplane Recalled for Display Failure After Power Save
Siemens is recalling five Artis Q biplanes because the display may fail to show an image after power save mode, potentially requiring procedure cancellation or patient transfer.
Product
Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide