State

Michigan product recalls

73,596 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: 1,562
Severe: 2,554
Most recent: 2026-10-24

Of the 9,551 recalls naming Michigan we have scored against our rubric, 1,562 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,554 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,551 recalls whose distribution notice names Michigan specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25201–25225 of 83147

SevereFDA (Food)·F-0227-2022·2021-12-08
Alsum Farms Red Onions Recalled Due to Salmonella Risk
Alsum Farms & Produce is recalling whole red onions in 2-pound bags due to potential Salmonella contamination. Affected bags have specific lot codes and were distributed in Illinois, Michigan, Pennsylvania, and Wisconsin.
Product
Alsum Farms & Produce Whole Red onions packaged in 2lb. (907g) bags, UPC 39186-60101 Produce of Mexico. Packed by Alsum Farms & Product, Inc., Friesland, WI 53935.
Category
Food
Distribution
4 states
HighCPSC·22027·2021-12-08
Mark of Fifth Avenue Children's Robes Recalled for Flammability Hazard
Mark of Fifth Avenue children's robes do not meet federal flammability standards for sleepwear and pose a risk of burn injuries. About 10,000 units sold online at Amazon and Walmart from August 2019 through June 2021 are affected.
Product
Children's robes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0321-2022·2021-12-08
Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss
Boston Scientific is recalling Hurricane RX dilation balloons used in endoscopic biliary procedures due to pinhole defects causing pressure loss that may prolong treatment.
Product
HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0327-2022·2021-12-08
FDA Recalls Hurricane RX Dilation Balloons for Pressure Failure Risk
Boston Scientific is recalling Hurricane RX Dilation Balloons nationwide due to pinhole defects that cause pressure loss or failure to maintain pressure during endoscopic procedures.
Product
HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545960
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0331-2022·2021-12-08
Siemens Dimension Vista 500 software issue affects test accuracy
Siemens is recalling 1,326 Dimension Vista 500 diagnostic devices worldwide due to incorrect default hemolysis, icterus, and lipemia indices that may affect test result accuracy.
Product
Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10284473 (US) and 10488224 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0315-2022·2021-12-08
INBONE Total Ankle System recalled for package-labeling mismatch
Wright Medical Technology is recalling INBONE Total Ankle System implants because the package contents and package labeling do not match.
Product
INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0320-2022·2021-12-08
Boston Scientific Hurricane RX Dilation Balloons Recalled for Pressure Loss Defect
Boston Scientific is recalling specific lots of Hurricane RX Dilation Balloons due to a pinhole defect that causes pressure loss, resulting in prolonged endoscopic procedures. Affected devices are used for dilating strictures in the bile duct.
Product
HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545890
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0322-2022·2021-12-08
Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect
Boston Scientific is recalling the Hurricane RX Dilation Balloon due to a pinhole defect causing pressure loss during endoscopic procedures. The defect may result in prolonged procedures and inability to effectively treat biliary strictures.
Product
HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN:M00545910
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0330-2022·2021-12-08
Dimension Vista 1500 Diagnostic Device: Incorrect HIL Index Defaults
Siemens is recalling 1,407 Dimension Vista 1500 diagnostic devices worldwide due to incorrect default Hemolysis, Icterus, and Lipemia (HIL) index values affecting five assays.
Product
Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10444801(US) and 10444802 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2022·2021-12-08
UV-C Germicidal Wand Recalled for Excessive Ultraviolet-C Radiation
MAX LUX CORP is recalling approximately 9900 handheld UV-C germicidal wands (Safe-T Lite) distributed nationwide due to excessive ultraviolet-C radiation emissions.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0242-2022·2021-12-08
Target Good & Gather Mixed Berry Sparkling Water Recall for Unlabeled Sulfites
Target Good & Gather Mixed Berry Sparkling Water in 8-packs is being recalled due to unlabeled sulfites. Keurig Dr Pepper discovered the issue after receiving complaints about off flavor and off aroma.
Product
Target Good & Gather Mixed Berry Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 11516 9, UPC outer Carton (8 pack): 0 85239 11345 5
Category
Food
Distribution
Distributed nationwide
HighCPSC·22028·2021-12-08
GE Appliances Recalls Free-Standing and Slide-In Ranges for Tip-Over Hazard
GE Appliances is recalling approximately 132,000 free-standing and slide-in electric and gas ranges because they can tip over if a heavy object is placed on an open oven door and the anti-tip-over bracket is not securely installed, risking burn injuries.
Product
Free-Standing and Slide-In Electric and Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0326-2022·2021-12-08
Boston Scientific HURRICANE RX Dilation Balloon Recalled for Pressure Loss
Boston Scientific is recalling HURRICANE RX Dilation Balloons due to a pinhole defect that causes pressure loss during endoscopic procedures. The device may fail to maintain necessary pressure, potentially prolonging procedures.
Product
HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545950
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0241-2022·2021-12-08
Target Good & Gather Coconut Pineapple Sparkling Water Recalled for Unlabeled Sulfites
Keurig Dr Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water because some cans contain unlabeled sulfites. The affected products were distributed nationwide.
Product
Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton (8 pack): 0 85239 03833 8
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0312-2022·2021-12-08
Blood Culture Identification Test Recalled Due to False Positive Risk
BioFire Blood Culture Identification 2 (BCID2) diagnostic panels are being recalled due to increased risk of false positive Acinetobacter calcoaceticus-baumannii results caused by non-viable contamination in blood culture vials.
Product
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog No./Description: 442023/BD BACTEC Plus Aerobic medium in plastic vials 442021/BD BACTEC Lytic Anaerobic medium in plastic vials 442192//BD BACTEC Plus Aerobic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0328-2022·2021-12-08
Cholesterol test system recalled due to calibration failure
RANDOX CHOL cholesterol test system is recalled due to a calibration defect that causes quality control results to be flagged as out of range. This could result in inaccurate cholesterol measurements in patient samples.
Product
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0318-2022·2021-12-08
Blood collection devices recalled due to premature needle retraction
Magnolia Medical Technologies is recalling Steripath Gen2 Blood Collection Systems due to an uptick in complaints of premature needle retraction during blood collection.
Product
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0239-2022·2021-12-08
7UP Zero Sugar Lemon Lime Soda Recalled for Unlabeled Sulfites
Keurig Dr Pepper is recalling 7UP Zero Sugar Lemon Lime Soda due to unlabeled sulfites detected after customer complaints about off flavor and aroma. The recall affects 9,152 cases distributed nationwide.
Product
7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0317-2022·2021-12-08
HALYARD STERLING ZERO Nitrile Exam Gloves Recall for Discoloration and Loss of Elasticity
O&M Halyard is recalling HALYARD STERLING ZERO nitrile exam gloves in all sizes due to discoloration and loss of elasticity with aging, making the gloves difficult or impossible to don without tearing. Approximately 5.86 million gloves distributed worldwide are affected.
Product
HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0308-2022·2021-12-08
Abbott HeartMate Touch System App may fail due to Bluetooth interference issue
The Abbott HeartMate Touch Communication System may experience temporary app failure when nearby Bluetooth devices attempt connections. Once properly connected, the system functions normally.
Product
Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0325-2022·2021-12-08
Hurricane RX Dilation Balloon Recalled Due to Pinhole Defect Causing Pressure Loss
Boston Scientific is recalling certain lots of the Hurricane RX Dilation Balloon due to a pinhole defect that causes loss of pressure or prevents the balloon from gaining or maintaining pressure during use, potentially prolonging medical procedures.
Product
HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545940
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0240-2022·2021-12-08
Polar Black Cherry Premium Seltzer recalled for unlabeled sulfites
Keurig Dr Pepper is recalling Polar Black Cherry Premium Seltzer 12-packs due to unlabeled sulfites. The recall affects 7,849 cases distributed nationwide with product code date 12/16/2022.
Product
Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0323-2022·2021-12-08
Boston Scientific HURRICANE RX Dilation Balloon Pressure Loss Recalled
Boston Scientific is recalling HURRICANE RX Dilation Balloons across the US due to pinhole defects that cause pressure loss during endoscopic procedures. The defect may prolong procedures and affect patient safety.
Product
HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545920
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0324-2022·2021-12-08
Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect
Boston Scientific is recalling the Hurricane RX Dilation Balloon nationwide due to a pinhole defect causing loss of pressure or failure to maintain pressure during endoscopic procedures used to treat biliary strictures.
Product
HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545930
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0329-2022·2021-12-08
GE Centricity Medical Imaging Software May Display Incomplete Patient Studies
GE Healthcare recalled versions of Centricity Universal Viewer Zero Footprint Client software due to a potential defect that could display incomplete patient imaging studies. No injuries have been reported.
Product
GE Centricity Universal Viewer Zero Footprint Client
Category
Medical Device
Distribution
Distributed nationwide