State

Minnesota product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53951–53975 of 81678

HighFDA (Food)·F-1418-2016·2016-06-15
Werner Brand Sweet Hot Crunch Mix Recalled for Undeclared Milk Allergen
Werner Gourmet Meat Snacks is recalling Sweet Hot Crunch Mix because the label declares butter but fails to declare milk, a major allergen.
Product
Werner Brand Sweet Hot Crunch Mix, net wt. 2 oz, UPC 7 09972 80120 1. Werner Brand Sweet Hot Crunch Mix, net wt. 6 oz, UPC 7 09972 80100 3. The ingredients statement declared: "***BUTTER TOFFEE PEANUTS (PEANUTS, SUGAR, BUTTER, SALT)***". The label contains…
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-1912-2016·2016-06-15
DePuy Synthes Flexible Shaft Reamers Recalled for Cytotoxicity Failure
Synthes (USA) Products LLC is recalling 244 DePuy Synthes 8.0 mm Flexible Shaft Reamers because they failed biological safety evaluations for cytotoxicity.
Product
DePuy Synthes 8.0 mm Flexible Shaft Reamer, 360 mm, Orthopedic manual surgical instrument. Part number 351.43
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1917-2016·2016-06-15
Zimmer Biomet Recalls Persona Trabecular Metal Tibial Plate Instruments
Zimmer Biomet is recalling specific Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets due to incidents of radiolucent lines and loosening in implants.
Product
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-1925-2016·2016-06-15
Berchtold Recalls Surgical Table Cushions Due to Potential Staple Contamination
Berchtold Corp. is recalling 227 HybriGel surgical table cushions because they may contain staples that could appear on patient x-rays.
Product
Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional accessory to the Operon Surgical Table. The pads may be attached to the base section with a Velcro fastener. The HybriGel pad shapes and variants can differ depending on the scope of the delivery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1423-2016·2016-06-15
Karlsburger Mesquite Seasoning Mix Recalled for Undeclared Soy Allergen
Karlsburger Foods is recalling 2 lb containers of Mesquite Seasoning Mix because they contain undeclared soy, a major food allergen.
Product
Karlsburger, Mesquite Seasoning Mix & Marinade, Item 46402, Net WT 2 lbs in plastic shaker jars.
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-1718-2016·2016-06-15
Philips Healthcare Ingenuity Core128 CT System Software Defect Recall
Philips Healthcare is recalling 423 Ingenuity Core128 CT systems in the US due to software defects that cause incorrect scan lengths and dose calculations.
Product
Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1937-2016·2016-06-15
Becton Dickinson Recalls 10 mL Syringes Due to Manufacturing Non-Conformities
Becton Dickinson is recalling 811,200 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.
Product
Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V438000·2016-06-15
Mercedes-Benz Recalls 2016 C300 Vehicles for Steering Software Error
Mercedes-Benz is recalling 2016 C300 4Matic vehicles because a software error may cause the electric power steering assist system to shut down, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ C300
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2016·2016-06-15
Sedecal Mobile X-ray System Recalled for Software Defect
Sedecal USA is recalling 145 mobile x-ray systems in the US due to a software defect that may apply adult exposure parameters to newborns.
Product
Sedecal SA Mobile Diagnost w DR x-ray system
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-1936-2016·2016-06-15
Becton Dickinson Recalls 10 mL Syringes Due to Manufacturing Issues
Becton Dickinson is recalling 176,000 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.
Product
Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1713-2016·2016-06-15
Philips Brilliance 64 CT System Software Defect Recall
Philips Healthcare is recalling 423 Brilliance 64 CT systems in the US due to software defects causing incorrect scan lengths and dose calculations.
Product
Philips Healthcare Brilliance 64 Computed Tomography X-Ray System
Category
Medical Device
Distribution
29 states
HighNHTSA·16V439000·2016-06-15
Mercedes-Benz Recalls 2016 SLK and SL Models for Headlight Aim
Mercedes-Benz is recalling certain 2016 SLK and SL models because low-beam headlights may be aimed incorrectly, potentially reducing driver visibility.
Product
MERCEDES-BENZ — MERCEDES-BENZ SLK300, SL63, SL550, SLK350
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16197·2016-06-15
Sony Recalls VAIO Laptop Battery Packs Due to Fire and Burn Hazards
Sony is recalling Panasonic lithium-ion battery packs for VAIO laptops because they can overheat, posing burn and fire hazards. No injuries have been reported.
Product
Panasonic battery packs used in Sony Electronics laptop computers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·16V436000·2016-06-15
Nissan Recalls 2016 Leaf and Sentra for Passenger Air Bag Wiring Defect
Nissan is recalling specific 2016 Leaf and Sentra vehicles because a wiring harness connector may disconnect, preventing the passenger air bag from deploying in a crash.
Product
NISSAN — NISSAN LEAF, SENTRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1417-2016·2016-06-15
Werner Butter Toffee Peanuts Recalled for Undeclared Milk Allergen
Werner Gourmet Meat Snacks, Inc. is recalling Werner Brand Butter Toffee Peanuts because the labels declared butter but failed to declare milk as an ingredient.
Product
Werner Brand Butter Toffee Peanuts, net wt. 2.25 oz, UPC 7 09972 80113 3 Werner Brand Butter Toffee Peanuts, net wt. 6 oz., UPC 7 09972 80027 3 The ingredients statement declared: Peanuts, Sugar, Butter, Salt. The label contains an advisory statement Allergen…
Category
Food
Distribution
19 states
HighFDA (Drugs)·D-0956-2016·2016-06-15
Novo Nordisk Recalls Norditropin Pens Due to Delivery System Defect
Novo Nordisk is recalling 723 Norditropin FlexPro pens due to a potential assembly fault that may cause the pen to block during the air shot step.
Product
NORDITROPIN — NORDITROPIN (SOMATROPIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1716-2016·2016-06-15
Philips Healthcare Ingenuity Core CT System Software Defect Recall
Philips Healthcare is recalling Ingenuity Core CT systems due to software defects that cause incorrect scan lengths and dose calculations.
Product
Philips Healthcare Ingenuity Core Computed Tomography X-Ray System
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1715-2016·2016-06-15
Philips Brilliance iCT SP CT System Recalled for Software Defects
Philips Healthcare is recalling Brilliance iCT SP CT systems due to software defects that cause incorrect scan lengths and dose calculations.
Product
Philips Healthcare Brilliance iCT SP Computed Tomography X-Ray System
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1914-2016·2016-06-15
Ortho VITROS 5600 System Recalled for Software Timing Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 5600 systems due to a software defect that may cause sample aspiration errors, leading to inaccurate or contaminated test results.
Product
VITROS 5600 Integrated System, Catalog Number 6802413, Unique Device Identifier No. 10758750002740; and VITROS 5600 Integrated System (refurbished), Catalog Number 6802915, Unique Device Identifier No. 10758750007110; IVD.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1913-2016·2016-06-15
Ortho VITROS 3600 Immunodiagnostic System Recalled for Software Timing Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 3600 systems due to a software timing anomaly that may cause the device to aspirate or dispense into unintended samples, potentially leading to erroneous or contaminated results.
Product
VITROS 3600 Immunodiagnostic System, Catalog Number 6802783,for use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1717-2016·2016-06-15
Philips Ingenuity CT System Recalled for Software Defects
Philips Healthcare is recalling Ingenuity CT systems due to software defects that cause incorrect scan lengths and dose calculations.
Product
Philips Healthcare Ingenuity CT Computed Tomography X-Ray System
Category
Medical Device
Distribution
29 states
ModerateFDA (Devices)·Z-1943-2016·2016-06-15
DePuy Synthes Recalls Norian Drillable Inject Due to Labeling Error
DePuy Synthes is voluntarily recalling Norian Drillable Inject 5 CC-Sterile units because the internal rotary pouch may be labeled with the incorrect powder volume, though the actual contents are correct.
Product
Norian Drillable Inject 5 CC-Sterile; catalog # 07.704.005S Intended for bony voids or defects of the extremities and pelvis that are not instrinsic to the stability of the bony structure.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1697-2016·2016-06-15
Ellipse ND: YAG Laser Applicator Recalled for Missing Calibration Instructions
Ellipse A/S is recalling 14 Ellipse ND: YAG Laser applicators because they lack required instructions for calibration procedures and schedules.
Product
Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1938-2016·2016-06-15
Teleflex Recalls Sterile Tracheal Tubes Due to Size Labeling Error
Teleflex Medical is recalling 6,390 sterile tracheal tubes because some units labeled as 7mm may actually be 7.5mm.
Product
Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex Incorporated. A tracheal tube is inserted into a patients mouth or nose for airway management.
Category
Medical Device
Distribution
23 states
ModerateFDA (Devices)·Z-1932-2016·2016-06-15
Beckman Coulter Uric Acid Reagent Recalled for False Low Results
Beckman Coulter is recalling Uric Acid reagent (OSR6x98) because Dipyrone may cause erroneous, false low results in assays.
Product
Uric Acid, Catalog No. OSR6x98 Product Usage:Uric acid OSR6x98 is intended as a System reagent for the quantitative determination of Uric Acid in human serum, heparinized plasma and urine on Beckman Coulter AU analyzers.
Category
Medical Device
Distribution
Distributed nationwide