The Recall Desk

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.

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.

48151–48175 of 81668

  • CriticalFDA (Food)·F-2215-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 1,196,880 units of Lays Kettle Cooked Multipack Trays nationwide due to the potential presence of Salmonella.

    Product
    30 count Lays Kettle Cooked Multipack Tray 41.25 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2213-2017·2017-05-17

    Frito-Lay Bold Mix Sack Recalled for Potential Salmonella Presence

    Frito-Lay is recalling 20-count Bold Mix Sacks nationwide due to the potential presence of Salmonella.

    Product
    20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2186-2017·2017-05-17

    Jimmy's Cookies Peanut Butter Chocolate Chunk Cookies Recalled for Undeclared Milk

    Jimmy's Cookies is recalling The Bakery Peanut Butter Chocolate Chunk Cookies because they may contain undeclared milk. The product was distributed nationwide.

    Product
    The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14 oz. (396g), packaged in a clear plastic clam shell, UPC 0 78742 06652 3, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2211-2017·2017-05-17

    Frito-Lay Recalls Jalapeño Flavored Potato Chips Due to Salmonella Risk

    Frito-Lay is recalling Jalapeño Flavored Lays Kettle Cooked and Miss Vickies Kettle Cooked potato chips due to a potential presence of Salmonella.

    Product
    Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape¿o Flavored Miss Vickies Kettle Cooked potato chips in the following unit sizes: 1.75 oz, 2.75 oz, 8 oz, 13.5 oz, 2.125 oz, 6.5 oz, 0.85 oz, 1.375 oz, 2.25 oz, and 1.375 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2214-2017·2017-05-17

    Frito-Lay Recalls Miss Vickies Multipack Trays Due to Potential Salmonella

    Frito-Lay is recalling 30-count Miss Vickies Multipack Trays nationwide and in Puerto Rico due to the potential presence of Salmonella.

    Product
    30 count Miss Vickies Multipack Tray 41.25 oz. packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2042-2017·2017-05-17

    Arthrex Recalls Anthrex PEEK SwiveLock SP Vented Anchors Due to Breakage

    Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion. The recall covers units distributed in the US and several international locations.

    Product
    Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2045-2017·2017-05-17

    Arthrex SpeedBridge Implant System Recalled for Broken Eyelets

    Arthrex is recalling specific SpeedBridge Implant Systems because some eyelets broke during insertion. The recall covers multiple batches distributed in the US and internationally.

    Product
    Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2050-2017·2017-05-17

    Mederi Stretta Catheter Recalled Due to Sterility Compromise

    Mederi Therapeutics is recalling 1,458 Stretta Catheter kits because a breach in the sterile barrier package compromised sterility.

    Product
    Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR ONLY. Used in the treatment of gastroesophageal reflux disease (GERD). REF 175-5580
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V324000·2017-05-17

    Isuzu Recalls NPR and GMC Trucks Due to Stuck Accelerator Pedal

    Isuzu is recalling certain 2008-2009 and 2012-2013 NPR, NPR HD, and GMC W3500/W4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.

    Product
    ISUZU — ISUZU, CHEVROLET, GMC NPR, W3500, W4500, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2068-2017·2017-05-17

    Zimmer Biomet Recalls Regenerex Patella Implants Due to Peg Shearing

    Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.

    Product
    Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2212-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 12-count Lays Kettle Cooked Multipacks nationwide due to potential Salmonella presence.

    Product
    12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2049-2017·2017-05-17

    Roche Diagnostics Recalls Sample Probes for Corrosion-Related Liquid Level Detection Issues

    Roche Diagnostics is recalling 3,946 sample probes for cobas analyzers because corrosion on electrical contacts can disrupt liquid level detection, potentially causing sample carryover.

    Product
    Sample probes associated with: cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 analyzer cobas c 501/502 cobas c 701/702 cobas 8000 ISE Product Usage: The cobas 6000 series is a fully automated, random-access, software-controlled system for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0705-2017·2017-05-17

    Teva Recalls Clozapine Tablets Due to Microbial Contamination

    Teva Pharmaceuticals is recalling specific lots of Clozapine Tablets USP, 25 mg, due to microbial contamination of non-sterile products.

    Product
    Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-4359-93), Individual Blister Pack (NDC 0093-4359-19), Rx Only, Manufactured By: Teva Pharmaceutical Industries Ltd., Jerusalem…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2200-2017·2017-05-17

    Pinnacle Foods Recalls Great Value Bread and Butter Chips for Glass Fragments

    Pinnacle Foods is recalling Great Value Bread and Butter Chips because glass fragments were found in the product. The chips were distributed nationwide.

    Product
    Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716 UPC 078742145990
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2046-2017·2017-05-17

    Arthrex Recalls Anthrex SpeedBridge Implant System Due to Broken Eyelets

    Arthrex, Inc. is recalling the Anthrex SpeedBridge Implant System because some eyelets broke from the SwiveLock Anchor during insertion.

    Product
    Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-2207-2017·2017-05-17

    Treehouse Foods Recalls Macaroni and Cheese Cups for Salmonella Risk

    Treehouse Foods is recalling specific brands of microwaveable macaroni and cheese cups because they may be contaminated with Salmonella.

    Product
    Macaroni & Cheese microwaveable cups sold under the following brands: 1. Big Win Original Macaroni & Cheese Dinner, UPC 11822-58403. 2. Cheese Club express mac Macaroni Cheese Dinner, UPC 41498-17167, 3. Great Value Macaroni & Cheese Dinner, UPC 78742-08249.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V325000·2017-05-17

    Bison Horse Trailers Recalled for Incorrect Weight Rating Labels

    Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.

    Product
    BISON — BISON LAREDO, TRAIL HAND, TRAIL BOSS, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17154·2017-05-17

    Cabrinha Recalls Kiteboard Control Systems Due to Injury and Fall Hazards

    Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.

    Product
    Cabrinha Kiteboard control systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2017·2017-05-17

    Arthrex Bio-SwiveLock SP Vented Anchor Recall Due to Broken Eyelets

    Arthrex, Inc. is recalling specific Bio-SwiveLock SP Vented anchors because some eyelets broke during insertion.

    Product
    Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-2043-2017·2017-05-17

    Arthrex Bio Composite SwiveLock Anchor Eyelets Break on Insertion

    Arthrex is recalling specific batches of Bio Composite SwiveLock anchors because some eyelets broke during insertion.

    Product
    Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-2040-2017·2017-05-17

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Patient ID Error

    Siemens is recalling 159 RAPIDPoint 500 Blood Gas Analyzers because a blank patient ID field may cause demographic errors.

    Product
    RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total hemoglobin, and hemoglobin derivatives in arterial, venous, and capillary whole blood samples.…
    Category
    Medical Device
    Distribution
    Distributed nationwide