State

Minnesota product recalls

72,936 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,804
Critical: 1,125
Severe: 1,892
Most recent: 2026-09-09

Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2876–2900 of 80740

HighFDA (Devices)·Z-1564-2026·2026-03-18
Medline surgical drapes may delaminate prematurely after recommended laundering
Medline is recalling five surgical drape products because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGN DBD-DRAPE,COVER,MAYO STAND,RESISTAT/XALT MDTZ1003656GN DBD-POCKET SHEET,RESISTAT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1518-2026·2026-03-18
Link Endo-Model plateau 15-8521/09 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/09 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/09;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1558-2026·2026-03-18
Lutronic Clarity II laser system reported sparking and popping during use
Lutronic is recalling the CLARITY II Laser System after reports of devices sparking or popping and potentially burning patients.
Product
CLARITY II Laser System; Model No. 1110200210.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1554-2026·2026-03-18
Artelon FlexBand Dynamic Matrix failed bacterial endotoxin testing
International Life Sciences is recalling the Artelon FlexBand Dynamic Matrix, ref 31057, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Dynamic Matrix Ref: 31057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1497-2026·2026-03-18
IBA proton therapy system may not interrupt beam when gating fails
Ion Beam Applications is recalling PROTEUS 235 proton therapy systems because a disabled interface means the safety system may not interrupt beam delivery if the external gating signal is lost.
Product
IBA Proton Therapy System - PROTEUS 235
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1551-2026·2026-03-18
EndoVive PEG kits recalled over compromised ChloraPrep swabstick seals
Boston Scientific is recalling EndoVive Safety PEG Kits containing BD ChloraPrep Triple Swabsticks because open or compromised seals on the swabstick packaging could cause loss of sterility.
Product
EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1511-2026·2026-03-18
Link Endo-Model SL component 16-2840/05 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/05 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1526-2026·2026-03-18
GEM Premier 5000 PAK part 00055360010 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2026·2026-03-18
Link Endo-Model SL component 16-2840/02 recalled over bushing fracture
Waldemar Link is recalling Endo-Model SL Connection Component item 16-2840/02 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1555-2026·2026-03-18
Artelon FlexBand Plus implants failed bacterial endotoxin testing
International Life Sciences is recalling Artelon FlexBand Plus, refs 41054 and 41057, because the augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Plus Ref: 41054 & 41057
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1520-2026·2026-03-18
Link Endo-Model plateau 15-8521/15 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/15 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/15;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1539-2026·2026-03-18
GEM Premier 5000 cartridges may eject repeatedly during analyzer warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 analyzers after confirmed complaints that GEM PAK cartridges may show increased Process Control Solution Not Detected errors during warm-up.
Product
GEM Premier 5000; Model No. 00055430010.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2026·2026-03-18
Beckman Coulter AU5800 analyzer may stop analyzing after database errors
Beckman Coulter is recalling Chemistry Analyzer AU5800 units because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1557-2026·2026-03-18
Vital Sync remote monitoring may not receive bedside monitor alarms
Covidien is recalling the HealthCast Vital Sync Remote Patient Monitoring System after complaints that alarms from the primary patient bedside monitor were not transmitted to or received by the remote system.
Product
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 /
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2026·2026-03-18
Raz shower commode chair seat may be reinstalled without engaging brackets
Raz Design is recalling several Mobile Shower Commode Chair models because a vendor modification means the seat may be reinstalled without properly engaging the outside rear seat brackets that hold it in place.
Product
Raz-AT (Attendant Tilt) Mobile Shower Commode Chair, Catalog Number Z300 UDI-DI code: (01)00628758003007 Raz-ART (Attendant Rotational Tilt) Mobile Shower Commode Chair, Catalog Number Z333 UDI-DI code: (01)00628758003335 Raz-AT600 (Bariatric Tilt) Mobile Shower Commode C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1519-2026·2026-03-18
Link Endo-Model plateau 15-8521/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-8521/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-8521/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1535-2026·2026-03-18
GEM Premier 5000 part 00055415010 may eject cartridges during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 part 00055415010 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000; Part No. 00055415010.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V162000·2026-03-18
Lexus NX, RX, and TX rearview camera software malfunction recall
Toyota is recalling certain 2022–2026 Lexus NX, RX, and TX vehicles because the rearview camera image may fail to display when the vehicle is in reverse, reducing rear visibility and increasing crash risk.
Product
LEXUS — LEXUS NX, RX, TX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1544-2026·2026-03-18
Infant and child defibrillator electrodes recalled over pediatric electrode delamination
Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes, catalogue numbers 11101-000016 and 11101-000017, due to pediatric defibrillator electrode delamination.
Product
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11101-000017 UDI-DI code: 00721902682483 Infant/Child Reduced Energy Defibrillation Electrodes are pre gelled, self-adhesive, the
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1521-2026·2026-03-18
Link Endo-Model plateau 15-0027/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-0027/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1510-2026·2026-03-18
Exactech Equinoxe core instrument kits may have handles missing cross-pins
Exactech is recalling the Equinoxe Core Instrument Kit, model KIT-311X, because the impactor handle may be missing a cross-pin.
Product
Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-1552-2026·2026-03-18
Beckman Coulter DxC 700 AU analyzer may stop analyzing after errors
Beckman Coulter is recalling DxC 700 AU analyzers because leaving the calibration monitor open beyond 15 minutes can trigger database errors that stop the system analyzing.
Product
DxC 700 AU, REF: B86444, B86446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1527-2026·2026-03-18
GEM Premier 5000 PAK part 00055360011 may eject during warm-up
Instrumentation Laboratory is recalling GEM Premier 5000 PAK part 00055360011 after confirmed complaints of Process Control Solution Not Detected errors during warm-up causing cartridge ejection.
Product
GEM Premier 5000 PAK; Part No. 00055360011.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V161000·2026-03-18
2026 Keystone Montana Fifth Wheel Recreational Trailers Electrical Wiring Recall
Keystone is recalling certain 2026 Montana fifth wheel trailers because improperly secured 12-volt and 120-volt wiring may be pinched and damaged when the bedroom slide-out moves, increasing fire risk.
Product
KEYSTONE — KEYSTONE MONTANA
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1549-2026·2026-03-18
Medartis APTUS 2.5 TriLock screw lots mixed with 2.8 mm
Medartis is recalling one lot of the APTUS 2.5 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.
Product
Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
Category
Medical Device
Distribution
Distributed nationwide