The Recall Desk

State

Minnesota product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44601–44625 of 81660

  • HighFDA (Food)·F-0598-2018·2018-01-24

    Ventura Foods Recalls Italian Dressing Due to Plastic Foreign Object

    Ventura Foods is recalling single-serve Italian dressing packets because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    Single-serve plastic packet Italian Dressing; Case packing: Sysco Classic Cls Italian 500 12Gm ; 47014SYS; B13017; single-serve plastic packet: Chef's Quality Creamy Italian; Chef's Quality; 60/1.5 OZ Pouches Net Wt 5.6 LB; 16689CHQ, B33317;
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0596-2018·2018-01-24

    Ventura Foods Recalls House Recipe Bleu Cheese Dressing Due to Plastic Foreign Object

    Ventura Foods is recalling 18 cases of House Recipe Bleu Cheese Dressing & Dip because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    plastic cup with foil seal: House Recipe Bleu Cheese Dressing & Dip; Distributed by: Sysco Corporation, Houston, Texas 77077; Net Wt 1.5 OZ.Code: B10127; packed in cardboard case : House Recipe; Distributed By Sysco Corporation; Houston Texas 77077; B10127; HR BluChs…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0382-2018·2018-01-24

    Owen Mumford Recalls Unifine Pentips Pen Needles Due to Sterility Concerns

    Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Consumers should check for discoloration on the protective seal.

    Product
    Unifine Pentips 5mm x 31G pen needles, packaged in 30 ct pen needles. Product Usage: Sterile, non-toxic, non-pyrogenic, single use pen needles for the subcutaneous injection of drugs from pen injectors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0220-2018·2018-01-24

    Pharmedium Recalls Subpotent Ephedrine Sulfate Syringes Nationwide

    Pharmedium Services is recalling 5,002 pre-filled ephedrine sulfate syringes nationwide because the drug was subpotent. The voluntary recall was initiated in October 2017.

    Product
    ePHEDrine Sulfate In 0.9% Sodium Chloride, 5 mg per mL (50 mg per 10 mL), 10 mL Total Volume pre-filled syringes, packaged in a) 5-count cartons, NDC 71030-0003-10 and NDC 71030-0003-20, and b) 25-count cartons, NDC 71030-0003-21 and NDC 71030-0003-12, Rx Only, PharMEDium…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0387-2018·2018-01-24

    Phadia 1000 Instrument Recalled Due to Retry Command Malfunction

    Phadia US Inc is recalling 70 Phadia 1000 Instruments nationwide because a malfunctioning Retry command may cause solution shortages and affect test results.

    Product
    Phadia 1000 Instrument, Article Number 12-3800-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0595-2018·2018-01-24

    Ventura Foods Recalls A&W Papa Sauce Due to Plastic Foreign Object

    Ventura Foods is recalling A&W Papa Sauce because a plastic foreign object was inadvertently introduced into the product stream.

    Product
    A&W All American Food Papa Sauce; 8/24 OZ. Pouches; Net Wt 12 LB. Paced Exclusively For Use By: A&W and its franchisees., Lexington, KY 40611; Use by: 04 29 18 and 04 30 18;
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0374-2018·2018-01-24

    Boston Scientific Recalls Pacemakers Due to Sensor Signal Issues

    Boston Scientific is recalling PROPONENT DR Pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.

    Product
    PROPONENT DR Pacemaker
    Category
    Medical Device
    Distribution
    50 states
  • HighNHTSA·18E006000·2018-01-24

    Dainese Recalls AGV Carbon Modular Helmets Due to Chin Bar Defect

    Dainese is recalling 325 AGV Carbon Modular motorcycle helmets because glue may have caused the chin base material to deteriorate, increasing injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide