The Recall Desk

State

Michigan product recalls

73,566 recalls have nationwide distribution and so reach Michigan. 9,551 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total
9,551
Critical
1,566
Severe
2,550
Most recent
2026-10-24

Of the 9,551 recalls naming Michigan we have scored against our rubric, 1,566 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,550 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,551 recalls whose distribution notice names Michigan specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22826–22850 of 83117

  • ModerateFDA (Drugs)·D-0979-2022·2022-06-08

    Hand Sanitizer Recalled for Improper Temperature Storage Conditions

    Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer due to storage outside of labeled temperature requirements, which may affect product efficacy.

    Product
    Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E Advanced Aloe Vera, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96537 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1194-2022·2022-06-08

    Busse Convenience Kits Recalled Due to Inadequate Manufacturing Test Validation

    Busse Hospital Disposables is recalling Convenience kits containing swab/swabstick drug products due to uncertainty about the validation of manufacturing test methods. The FDA classified this as a Class II recall.

    Product
    Female SS 3.5MM Pellet Insertion Tray Catalog Number: B1568
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1183-2022·2022-06-08

    Busse Hospital Swab Products Recalled for Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling swab and swabstick drug products due to uncertainty about whether manufacturing test methods were adequately validated. No illnesses or injuries have been reported.

    Product
    SS 3.5MM Pellet Insertion Tray with Medium Gloves Catalog Number: B1354
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1223-2022·2022-06-08

    Medtronic NIM Vital Console 4.0 Surgical Nerve Monitoring Device Software Anomaly Recall

    Medtronic Xomed is recalling 18 units of the NIM Vital Console 4.0 surgical nerve monitoring device due to an identified software anomaly. Distribution was confirmed in Texas, Colorado, New Jersey, and France.

    Product
    NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1191-2022·2022-06-08

    Busse Convenience Kits Recalled Due to Manufacturing Test Validation Uncertainty

    Busse Convenience kits containing swab/swabstick drug products from Professional Disposables International are being recalled due to uncertainty about test method validation during manufacturing. The affected products include lot numbers 2110053 and 2110115, representing 60 units distributed nationwide.

    Product
    SS 3.5MM Diamond Tip Trocar - Medium Gloves Catalog Number: B1555
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1181-2022·2022-06-08

    Medical swab insertion tray recalled due to manufacturing validation uncertainty

    Busse Hospital Disposables recalls swab insertion trays due to uncertainty about manufacturing test method validation. The Class II recall affects products nationwide.

    Product
    SS 3.5Mm Pellet Insertion Tray with large Gloves Catalog Number: B1352
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1224-2022·2022-06-08

    Medical Device Patient Interface Recalled Due to Software Anomaly

    Medtronic is recalling the NIM Vital Patient Interface 4.0 due to a software anomaly identified in the device. The recall affects 29 units distributed worldwide, including in the US and France.

    Product
    NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0975-2022·2022-06-08

    Family Dollar AMBI Skincare Sunscreen Recalled for Improper Storage

    Family Dollar is recalling an AMBI Skincare Even & Clear Nourishing Daily Facial Moisturizer (SPF 30) for improper storage. The product may have reduced efficacy.

    Product
    Only At Family Dollar AMBI Skincare Even & Clear Nourishing Daily Facial Moisturizer With Broad Spectrum SPF 30 Sunscreen, Net Wt. 1.7 FL. OZ. (50 mL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1150-2022·2022-06-08

    Lumbar Tray with Swab Products Recalled Due to Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling Lumbar Tray units nationwide because test methods used during manufacturing could not be adequately validated. The recall affects swab/swabstick products used in medical procedures.

    Product
    Lumbar Tray Catalog 1091
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0972-2022·2022-06-08

    Losartan Potassium tablets recalled for excessive AZIDO impurity

    Strides Pharma is recalling approximately 200,407 bottles of Losartan Potassium 25 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1164-2022·2022-06-08

    Busse Convenience Kits Swabs Recalled Due to Testing Validation Uncertainty

    Busse Hospital Disposables is recalling Busse Convenience Kits containing medical swabs and swabsticks due to uncertainty about test method validation in manufacturing. No illnesses reported.

    Product
    Pain Tray Catalog Number: 9883
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1159-2022·2022-06-08

    Single Shot Epidural Tray Recalled Due to Test Validation Uncertainty

    Single Shot Epidural Trays made by Busse Hospital Disposables are being recalled nationwide due to inadequate validation of the test methods used to manufacture the product. The recall affects 400 units.

    Product
    Single Shot Epidural Tray Catalog Number: 8417
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1146-2022·2022-06-08

    FDA recalls APD Drain Manifold units lacking regulatory clearance

    Baxter Healthcare is recalling 180 APD Drain Manifold units distributed in nine US states because certain product codes lack FDA regulatory clearance. Patients using affected units should contact Baxter Healthcare immediately.

    Product
    APD Drain Manifold
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1168-2022·2022-06-08

    Cervical Tray Recalled for Manufacturing Test Method Validation Uncertainty

    Busse Hospital Disposables is recalling Cervical Tray Catalog Number 3765R2 units containing swab products due to uncertainty about the adequacy of manufacturing test method validation. Lot Numbers 2031213S and 2130221S are affected.

    Product
    Cervical Tray Catalog Number: 3765R2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1151-2022·2022-06-08

    Busse Hospital Epidural Trays Recalled for Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling Single Shot Epidural Trays due to uncertainty about whether manufacturing test methods were adequately validated. No illnesses or injuries have been reported.

    Product
    Single Shot Epidural Tray Catalog 1165
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1197-2022·2022-06-08

    Drug Swab Products Recalled for Manufacturing Validation Uncertainty

    Busse Convenience kits containing swab/swabstick drug products made by PDI are being recalled due to uncertainty about validation testing adequacy in manufacturing. Users should discontinue use of affected lot numbers.

    Product
    3.2MM Pellet Insertion Tray Catalog Number: B7345R1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V398000·2022-06-07

    C.E. Smith and Malone Auto Racks Recall Boat Trailers Due to Axle Weld Failure

    C.E. Smith is recalling 2021-2022 boat trailers because a weld may fail, causing the wheel to separate and increasing crash risk.

    Product
    MALONE AUTO RACKS — MALONE AUTO RACKS, C.E. SMITH COMPANY MICROSPORT MPG460, MULTI-SPORT 48810, ECOLIGHT MPG585, MULTI-SPORT 48815
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V400000·2022-06-07

    Off Grid Trailers Recalls 2021-2022 Models Due to Gas Leak Risk

    Off Grid Trailers is recalling 2021-2022 Expedition, Pando, and Switchback travel trailers because damaged burner control valves may cause a gas leak.

    Product
    OFF GRID TRAILERS — OFF GRID TRAILERS EXPEDITION, SWITCHBACK, PANDO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22C002000·2022-06-07

    Clek Recalls Olli and Ozzi Booster Seats Due to Missing Label

    Clek is recalling Olli and Ozzi booster seats because a required installation diagram is missing, which could lead to improper installation and increased injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V397000·2022-06-07

    Kawasaki Recalls LX230 Motorcycles Due to Brake Rotor Defect

    Kawasaki is recalling 2020-2022 LX230 motorcycles because an incorrect front brake rotor may have been installed, reducing brake performance and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI LX230G, LX230A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V401000·2022-06-07

    2021-2022 Mack trucks recalled for defective steering gears

    Mack Trucks is recalling certain 2021-2022 tractor trailers due to steering gears that may fracture, causing loss of steering control and crash risk.

    Product
    MACK — MACK PINNACLE (PI/PN), TE, ANTHEM (AN), GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V396000·2022-06-06

    Micro Bird Recalls 2017-2018 G5 School Buses Due to Seat Belt Defect

    Micro Bird is recalling 2017-2018 G5 school buses because an incorrect bracket may interfere with the driver's seat belt pretensioner, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V395000·2022-06-06

    Forest River Recalls 2022 Travel Trailers Due to Table Weld Defect

    Forest River is recalling 2022 East to West Alta and Palomino SolAire travel trailers because incomplete welds on the swing-up table base may cause it to drop unexpectedly, increasing injury risk.

    Product
    PALOMINO — PALOMINO, EAST TO WEST SOLAIRE, ALTA
    Category
    Vehicle
    Distribution
    Distributed nationwide