The Recall Desk

State

Minnesota product recalls

20,304 recalls have nationwide distribution and so reach Minnesota. 0 additional recalls listed Minnesota specifically in their distribution scope.

About recalls in Minnesota

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Minnesota consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11926–11950 of 20304

  • SevereFDA (Devices)·Z-2374-2023·2023-08-23

    Dialysis Catheter Recall: Center Lumen Occlusion Due to Excessive Lubricant

    Covidien LP is recalling MAHURKAR 12 Fr dialysis catheters due to center lumen occlusion from excessive lubricant. The defect may cause treatment delays and serious complications including embolism and thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, PASS Tray REF: 8888103002HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2391-2023·2023-08-23

    Dialysis Catheter Recalled for Center Lumen Occlusion Risk

    Covidien LP is recalling 3,965 MAHURKAR dialysis catheters due to excessive lubricant causing center lumen occlusion. This may obstruct blood flow or cause hemolysis and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, Kit REF: 8888345637HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2411-2023·2023-08-23

    Alcon Custom Pak Intraocular Lens Packages Recalled for Plastic Debris Risk

    Alcon Custom Pak intraocular lens packages are recalled due to reports of patient injury during surgical procedures caused by plastic debris from over-tightening with the included plastic wrench.

    Product
    Alcon Custom Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2385-2023·2023-08-23

    Acute Dialysis Catheter Recalled for Potential Lumen Obstruction and Embolism Risk

    Covidien is recalling MAHURKAR acute dialysis catheters for excessive silicone lubricant causing lumen obstruction that may delay treatment and lead to hemolysis, embolism, or thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit REF: 8888345603HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2407-2023·2023-08-23

    Centurion FMS Pak Recalled Due to Patient Injury Risk from Plastic Debris

    Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.

    Product
    Centurion FMS Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2023·2023-08-23

    HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard

    Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.

    Product
    HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8) A2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2405-2023·2023-08-23

    Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm

    Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.

    Product
    CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2401-2023·2023-08-23

    UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage

    Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.

    Product
    UroPass Ureteral Access Sheaths, 5 pieces/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1084-2023·2023-08-23

    Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons

    Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.

    Product
    hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-p
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2414-2023·2023-08-23

    FreeStyle Libre 2 Readers may fail to activate new sensors

    FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.

    Product
    FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1086-2023·2023-08-23

    Tobramycin Ophthalmic Solution recalled for failed quality specifications

    Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.

    Product
    TOBRAMYCIN OPHTHALMIC SOLUTION — TOBRAMYCIN OPHTHALMIC SOLUTION (TOBRAMYCIN OPHTHALMIC SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1085-2023·2023-08-23

    PLUVICTO Injection Recalled for Incorrect Lot and Expiration Date Labels

    PLUVICTO (lutetium Lu 177 vipivotide tetraxetan) injection vials were labeled with incorrect lot numbers and expiration dates. The manufacturer is recalling affected lots distributed nationwide.

    Product
    PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2412-2023·2023-08-23

    Medtronic ventricular catheter system recalled due to incorrect labeling expiration date

    Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.

    Product
    Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·23263·2023-08-17

    Zipadee Kids Convertible House Bed Frames Recalled for Entrapment and Strangulation Risk

    Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds are being recalled due to spindle spacing that can trap a child's torso while preventing their head from passing through, creating a strangulation hazard. At least two children have become entrapped.

    Product
    Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23783·2023-08-17

    Ubio Labs power banks recalled due to fire hazard

    Costco is recalling approximately 350,000 Ubio Labs power banks (model PWB1071) that can overheat and ignite. The company has received three fire reports, including one on a commercial flight with four smoke inhalation reports and one minor burn injury.

    Product
    Ubio Labs power banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23782·2023-08-17

    Midwest Lubricants Sodium Hydroxide Recalled for Unsafe Packaging

    Midwest Lubricants is recalling about 3,000 units of Sodium Hydroxide (Caustic Soda Beads) because the packaging is not child-resistant and the label lacks required hazard information. The product poses a risk of chemical burns and eye irritation.

    Product
    Midwest Lubricants Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23265·2023-08-17

    Simplay3 Toddler Towers Recalled Due to Fall and Injury Hazards

    Simplay3 Toddler Towers can tip over during use, posing fall and injury hazards to young children. The manufacturer has received 16 reports of tipping, including 10 reports of injuries.

    Product
    Simplay3 Toddler Towers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23262·2023-08-16

    Gree Recalls 1.56 Million Dehumidifiers Due to Fire and Burn Hazards

    Gree is recalling approximately 1.56 million dehumidifiers sold under brand names including GE, Kenmore, SoleusAir, Seabreeze, and Norpole because they can overheat, smoke, and catch fire, creating fire and burn hazards.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1401-2023·2023-08-16

    Cava Spicy Hummus recalled nationwide for undeclared sesame

    Cava Spicy Hummus (8oz, UPC 89832800227) is being recalled because it contains undeclared sesame. The product was distributed nationwide; consumers with sesame allergies may be at risk.

    Product
    Cava Spicy Hummus UPC 89832800227 Net Wt. 8oz./226.8 g Packaged in clear plastic container. 12 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1421-2023·2023-08-16

    Food Recall: ONO Vegan Blueberry Protein Overnight Oats for Undeclared Milk

    ONO LLC is recalling ONO Vegan Blueberry Muffin Protein Overnight Oats because they contain undeclared milk, a common allergen. The product was distributed nationwide and poses a risk to consumers with milk allergies.

    Product
    ONO Vegan Blueberry Muffin Protein Overnight Oats, 2.75oz. UPC 01-95893-47024-2
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1366-2023·2023-08-16

    Energy balls recalled for undeclared sesame allergen

    Betty Lou's Paleo Java Nuts About Energy Balls are being recalled due to undeclared sesame in the product. The recall affects packages distributed nationwide.

    Product
    Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds, shelf-stable, 12-month shelf life, 1.5 oz (42g) package and 12/1.5 oz. packages per display box. Packages are sold individually (UPC 0 1607352146 5) or packaged into 12-ct display box (UPC 0 16073
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2361-2023·2023-08-16

    Siemens ARTIS Angiography Systems: Thermal Overload Risk in Cable Connectors

    Siemens has recalled 10 ARTIS angiography systems due to thermal overload hazard in cable connectors. The issue may cause burning smell and loss of imaging functionality, potentially requiring treatment cancellation or system replacement.

    Product
    ARTIS pheno-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2341-2023·2023-08-16

    Olympus LF-P Tracheal Intubation Fiberscope Sterilization and Compatibility Update

    Olympus is updating labeling for 686 LF-P fiberscopes to clarify they are no longer compatible with OER reprocessors and specify new 100% ETO sterilization protocol.

    Product
    Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Olympus Light Source, documentation equipment, display monitor and other ancillary equipment for management of Endotracheal Tube
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2350-2023·2023-08-16

    Hip stem trial instruments recalled due to excessive removal force

    LINK MP Monoblock hip stem trial instruments may require excessive force to remove after impaction, potentially prolonging surgery or requiring procedural modification.

    Product
    LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 19-Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-119/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2396-2023·2023-08-16

    Ingenia Elition S MR System smoke detection interlock vulnerable to operator bypass

    Philips Ingenia Elition S MR systems can be circumvented by power cycling to bypass the smoke detection safety interlock that locks after smoke is detected. This could allow continued operation despite fire hazards.

    Product
    Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
    Category
    Medical Device
    Distribution
    Distributed nationwide