State

Minnesota product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45526–45550 of 81668

SevereFDA (Drugs)·D-1177-2017·2017-10-04
Pfizer Recalls Sterile Water for Injection Vials Due to Cracked Glass
Pfizer is recalling 18,725 vials of Sterile Water for Injection due to cracked or chipped glass at the neck, which poses a non-sterility risk.
Product
Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3196-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 3.5 mm Diameter 110 mm Length, Item Number/EDI 00480611035, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V618000·2017-10-04
Prevost Recalls Motor Coaches Due to Fuel Tank Cradle Defect
Prevost is recalling 2008-2018 motor coaches because fuel tank cradles may loosen, causing the tank to fall off and increasing crash risk.
Product
PREVOST — PREVOST X3-45 VIP ENTERTAINER, X3-45 VIP, XL2, H3-45 VIP
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3106-2017·2017-10-04
Spectranetics Bridge Occlusion Balloon Catheter Recalled for Guidewire Issues
Spectranetics is recalling Bridge Occlusion Balloon catheters because the guidewire may not pass through the device, potentially delaying treatment.
Product
Spectranetics Bridge Occlusion Balloon catheter, Sheath Compatibility 12F, Guidewire Compatibility 0.035in, Working Length 90cm, Balloon Outer Diameter 31mm, Balloon Length 80mm, Rx Only. Product Usage: It is a device used to occlude the vessel and prevent blood loss as the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3175-2017·2017-10-04
Zimmer Biomet Recalls Straight Shank Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 62 units of 4.0 mm Straight Shank Drill Bits because raw material anomalies may increase the risk of instrument fracture during use.
Product
Straight Shank Drill Bits 4.0 mm Diameter, Item Number/EDI 00231804006, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3202-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 150 nonsterile orthopedic drill bits because raw material anomalies may cause the instruments to fracture during use.
Product
Drill Bit Quick-Connect 4.5 mm Diameter 145 mm Length, Item Number/EDI 00480614545, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3199-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 15 nonsterile orthopedic drill bits because raw material anomalies may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 3-Fluted 4.5 mm Diameter 195 mm Length, Item Number/EDI 00480719545, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3231-2017·2017-10-04
Sorin Platinium VR ICDs Recalled for Potential Overconsumption Risk
Sorin Group is recalling 72 Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Product
Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3167-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fixation Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling ECT Internal Fixation Drill Bits because raw material anomalies may cause the instruments to fracture during use.
Product
ECT Internal Fixation Drill Bits 2.5 mm Diameter (0.98 Inch), Item Number/EDI 00231802506, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3158-2017·2017-10-04
Zimmer Biomet Recalls M/DN Intramedullary Fixation Distal Drill Pilot Tips
Zimmer Biomet is recalling 182 M/DN Intramedullary Fixation Distal Drill Pilot Tips due to raw material anomalies that may increase the risk of instrument fracture.
Product
M/DN Intramedullary Fixation Distal Drill Pilot Tip 3.2 mm Diameter, Item Number/EDI 00225503332, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V617000·2017-10-04
Hyundai Sonata Seat Belt Linkage Recall for Detachment Risk
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles previously repaired under a prior campaign because seat belt linkages may detach from pretensioners, increasing injury risk in a crash.
Product
HYUNDAI — HYUNDAI SONATA HYBRID, SONATA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3228-2017·2017-10-04
Sorin Platinium VR ICDs Recalled for Potential Overconsumption Risk
Sorin Group is recalling Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Product
Platinium VR 1210, Model Number TDF031U, UDI/GTIN 08031527015514, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3187-2017·2017-10-04
Zimmer Biomet Recalls ECT Quick-Connect Drills Due to Fracture Risk
Zimmer Biomet is recalling 62 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may cause the instruments to fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 3.5 mm Diameter 11 cm Length, Item Number/EDI 00241003500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V619000·2017-10-04
Lexus Recalls 2010 HS 250h Hybrid for Transaxle Short Circuit Risk
Toyota is recalling 2010 Lexus HS 250h Hybrid vehicles because a hybrid transaxle component may short circuit, causing a loss of power and increasing crash risk.
Product
LEXUS — LEXUS HS 250 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3191-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.
Product
Drill Bit Jacobs Chuck 3.2 mm Diameter 130 mm Length, Item Number/EDI 00480513032, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3188-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Quick-Connect Drill Bits
Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Quick-Connect Drills due to a raw material anomaly that may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 4.0 mm Diameter 20cm Length, Item Number/EDI 00241004000, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3157-2017·2017-10-04
Zimmer Biomet Recalls NCB Periprosthetic Plate System Drill Bits
Zimmer Biomet is recalling 185 NCB Periprosthetic Plate System Drill Bits due to a raw material anomaly that may increase the risk of instrument fracture during use.
Product
NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 4.5 mm Diameter 195 mm Length, Item Number/EDI 0200024330, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V620000·2017-10-04
Grand Design Recalls 2017-2018 Imagine Trailers for Fire Risk
Grand Design RV is recalling 2017-2018 Imagine recreational trailers because air conditioning wires may detach and short circuit, increasing fire risk.
Product
GRAND DESIGN — GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3150-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Quick-Connect Drills
Zimmer Biomet is recalling 4 units of ECT Internal Fracture Fixation Quick-Connect Drills due to raw material anomalies that may increase the risk of instrument fracture.
Product
ECT Internal Fracture Fixation Quick-Connect Drill, 1.5 mm Diameter, 85mm Length, Item Number/EDI 00241001500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3178-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Screw Taps Due to Material Anomaly
Zimmer Biomet is recalling 198 nonsterile orthopedic screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Product
Zimmer Periarticular Locking Plate System, Locking Screw Tap Standard Quick-Connect 3.5 mm Diameter, Item Number/EDI 00236015335, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3160-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Instruments Due to Fracture Risk
Zimmer Biomet is recalling 21 units of M/DN Intramedullary Fixation Femoral Drills because raw material anomalies may cause the instruments to fracture during use.
Product
M/DN Intramedullary Fixation Femoral Drill Large 5.0 mm Item Number/EDI 00225503550, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3180-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Drills Due to Fracture Risk
Zimmer Biomet is recalling 1,091 nonsterile orthopedic surgical drills and screw taps because raw material anomalies may cause instrument fracture.
Product
Zimmer Periarticular Locking Plate System Drill Standard 2.0 mm Diameter, Item Number/EDI 00236017520, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3193-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because a raw material anomaly may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 2.0 mm Diameter 100 mm Length, Item Number/EDI 00480610020, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3224-2017·2017-10-04
Teleflex Percuvance Surgical System Recalled for Connection and Tip Defects
Teleflex Medical is recalling Percuvance 29cm Shaft surgical systems because the shaft connection may be compromised or tool tips may close abruptly.
Product
Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft tissue…
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-3162-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Drills Due to Material Anomaly
Zimmer Biomet is recalling 1,999 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Drill 1.5 mm Diameter (.059 Inch), Item Number/EDI 00231801500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide