State

Michigan product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22276–22300 of 83060

HighFDA (Drugs)·D-1143-2022·2022-06-22
Prefilled Syringes of Medroxyprogesterone Acetate Recalled for Lack of Sterility Assurance
Afaxys Pharma is recalling 79,339 prefilled syringes of medroxyprogesterone acetate because the manufacturer could not assure sterility. The syringes were distributed nationwide.
Product
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by: Sun Pharmaceutical Industries, Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India Distributed by: Afaxys Pharma, LLC, Charleston, SC, 29403, USA, Product…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1259-2022·2022-06-22
Illumina MiSeq Dx Sequencing Instruments Recalled Due to Cybersecurity Vulnerability
Illumina is recalling approximately 1,014 MiSeq Dx sequencing instruments due to a cybersecurity vulnerability. The devices are distributed worldwide and throughout the United States.
Product
illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1297-2022·2022-06-22
Cedar Crest Caramel Collision Ice Cream Recalled for Plastic Contamination
Cedar Crest Caramel Collision Ice Cream is being recalled due to the presence of plastic foreign material in the product. The affected product was distributed across IL, MI, MN, TX, and WI.
Product
Cedar Crest Caramel Collision Ice Cream, Net Wt. 1.5 Quarts (1.41 L). UPC 20652-00714. Caramel Ice Cream with a Caramel Swirl and Chocolate coated Caramel Mini Cups. Cedar Crest Specialties, Inc. Cedarburg, WI 53012
Category
Food
Distribution
5 states
HighFDA (Drugs)·D-1126-2022·2022-06-22
Homeopathic drug Bacillinum Pulmo recalled for manufacturing deviations
Washington Homeopathic Products recalled Bacillinum Pulmo homeopathic drug due to manufacturing practice deviations. The Class II recall, initiated in May 2022 and terminated in May 2023, affected nationwide distribution.
Product
Bacillinum Pulmo, Potency: 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1267-2022·2022-06-22
Medtronic Cobalt ICD and CRT-D Telemetry Software Error Recall
Medtronic is recalling Cobalt and Crome ICDs and CRT-Ds due to a software telemetry error in the CareLink SmartSync Device Manager. The error may affect device communication and remote monitoring.
Product
Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1, DVPA2D4; b) Cobalt VR: DVPB3D1, DVPB3D4; c) Cobalt XT DR: DDPA2D1, DDPA2D4; d) Cobalt DR: DDPB3D1, DDPB3D4; e) Cobalt XT HF: DTPA2D4, DTPA2D1 f) Cobalt…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V441000·2022-06-22
2023 Thomas Built Saf-T-Liner C2 School Buses Recalled for Emergency Exit Defect
Daimler Trucks North America is recalling 2023 Thomas Built Saf-T-Liner C2 school buses because they may lack sufficient emergency exits, increasing injury risk during emergencies.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1376-2022·2022-06-22
Dawn's Campfire BBQ Beans Recalled for Metal Foreign Object
Morski Brands recalls 1,312 units of Dawn's Campfire BBQ Beans nationwide due to metal foreign objects. Consumers should not consume the product.
Product
Dawn's Campfire BBQ Beans, #90125, Net Wt 8 lb (3.63 kg) Keep Refrigerated UPC 0 32345 90125 4. Mfg By Morski Brands, Inc., Portage, WI 53901
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1146-2022·2022-06-22
Medroxyprogesterone acetate injectable suspension recalled for lack of sterility assurance
Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension (150 mg/mL) nationwide due to lack of assurance of sterility. Affected lots contain vials with expiration dates from December 2022 through September 2023.
Product
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Manufactured for: Northstart Rx LLC, Memphis, TN, 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1374-2022·2022-06-22
Ranch BLT Pasta Salad Recalled for Metal Foreign Objects
Morski Brands recalls Ranch BLT Pasta Salad nationwide due to possible metal fragments. The product was sold under Finest Traditions and Dawn's brands with a best-before date of 6-13-22.
Product
Ranch BLT Pasta Salad, Keep Refrigerated packaged in the following brands and plastic container sizes: 1. Finest Traditions, Net Wt. 2/5 lbs. (10 lbs) (4.54kg), Item 10406332. UPC 10 7 33147 11722 1. Distributed By: DBC Foods, St. Cloud, MN 56302. 2. Dawn's…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1262-2022·2022-06-22
Olympus endoscope diopter ring adhesive failure may impair vision
Olympus endoscopes with defective diopter ring adhesive may cause vision loss and, in rare cases, urinary tract perforation.
Product
Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5
Category
Medical Device
Distribution
9 states
HighFDA (Drugs)·D-1135-2022·2022-06-22
Homeopathic drug Proteus recalled for manufacturing quality control deviations
Washington Homeopathic Products is recalling Proteus homeopathic remedy in multiple potencies due to manufacturing process deviations. The firm initiated this voluntary recall in May 2022.
Product
Proteus, Potency: 7C, 8C, 9C, 12C, 15C, 16C, 20C, 30C, 200C, OTC, Liquid Pellets, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V443000·2022-06-22
2022 Freightliner Cascadia brake system may fail to engage
The emergency braking system on certain 2022 Freightliner Cascadia trucks may fail to engage, creating a risk of brake failure. Dealers will install a corrective valve at no cost.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1373-2022·2022-06-22
Steakhouse Potato Salad Recalled Due to Metal Contamination
Morski Brands is recalling Steakhouse Potato Salad products nationwide due to metal contamination. Affected brands include Finest Traditions and Dawn's.
Product
Steakhouse Potato Salad, Keep Refrigerated packaged in the following brands and plastic container sizes: 1. Finest Traditions, Net Wt. 10 lb (4.54kg), Item 1038364. UPC 10-73314710773-4. Mfg By Morski Brands, Inc., Portage, WI 53801. 2. Finest Traditions, Net Wt.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1268-2022·2022-06-22
Medtronic Crome and Cobalt Cardiac Defibrillators Recalled Due to Telemetry Error
Medtronic recalls 3,944 Crome and Cobalt ICDs and CRT-Ds due to a potential telemetry error affecting device communication with external monitors.
Product
Crome Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Crome VR: DVPC3D1, DVPC3D4; b) Crome DR: DDPC3D1, DDPC3D4; c) Crome HF: DTPC2D4, DTPC2D1; d) Crome HF Quad: DTPC2QQ, DTPC2Q1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1150-2022·2022-06-22
Zileuton Extended-Release Tablets recalled for failed dissolution specifications
Lupin Pharmaceuticals is recalling Zileuton Extended-Release Tablets, 600 mg, due to failed dissolution specifications found during stability testing that may affect medication efficacy.
Product
Zileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 by Lupin Limited, Nagpur-441108, India, NDC 68180-169-16
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1260-2022·2022-06-22
Illumina NextSeq 550 Genetic Sequencer Cybersecurity Vulnerability Recall
Illumina is recalling 799 NextSeq 550 Dx genetic sequencers due to a cybersecurity vulnerability in the Local Run Manager software. Affected devices have been distributed worldwide and in the United States.
Product
illumina Model NextSeq 550 Dx REF 20005715
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1263-2022·2022-06-22
Olympus Uretero-Reno Fiberscope Recalled for Defective Adhesive and Vision Loss
The Olympus URETERO-RENO FIBERSCOPE Model URF-P6 is recalled for incorrect adhesive securing the diopter ring. The defect may cause loss of adjustment function, blurred vision, and in rare cases, urinary tract perforation.
Product
Olympus URETERO-RENO FIBERSCOPE Model: URF-P6
Category
Medical Device
Distribution
9 states
HighFDA (Food)·F-1377-2022·2022-06-22
Finest Traditions Smokey Baked Beans recalled for potential metal contamination
Morski Brands, Inc. is recalling 2,648 units of Finest Traditions Smokey Baked Beans due to the potential presence of foreign metal objects. The recalled product was distributed nationwide.
Product
Finest Traditions Smokey Baked Beans, #1038700, Net Wt 8 lb (3.63 kg) Keep Refrigerated UPC 10 7 33147 10231 9. Distributed By: DBC Foods, St Cloud, MN 56302
Category
Food
Distribution
Distributed nationwide
HighNHTSA·22V442000·2022-06-22
2022 Grand Design Momentum Travel Trailer Electrical Fire Hazard Recall
Grand Design is recalling 165 model-year 2022 Momentum travel trailers due to improper 110-volt electrical wiring that can overheat and create a fire risk. Dealers will rewire the power supply at no cost.
Product
GRAND DESIGN — GRAND DESIGN MOMENTUM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1378-2022·2022-06-22
Potato Salad Recalled Nationwide for Metal Contamination Risk
Morski Brands recalled 832 units of Dawn's Smoked Gouda & Bacon Potato Salad due to possible metal fragments. Consumers with products bearing best-before dates 5-13-22, 6-21-22, 6-24-22, or 6-27-22 should not consume them.
Product
Dawn's Smoked Gouda & Bacon Potato Salad, #10079, Net Wt 8 lb (3.63 kg) Keep Refrigerated. UPC 10032345130019. Mfg By Morski Brands, Inc., Portage, WI 53901
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1144-2022·2022-06-22
Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Assurance Failure
Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension due to lack of assurance of sterility. The recall affects approximately 57,997 prefilled syringes distributed nationwide.
Product
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1130-2022·2022-06-22
Homeopathic Drug Diphtherinum Recalled for Manufacturing Practice Deviations
Washington Homeopathic Products is recalling Diphtherinum homeopathic remedy (potencies 14C, 30C, 200C) distributed nationwide due to manufacturing practice deviations (cGMP violations). Affected lots: 20332, 20333.
Product
Diphtherinum, Potency: 14C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1127-2022·2022-06-22
Homeopathic Drug Recall: Candida Albicans Remedy for Manufacturing Quality Issues
Washington Homeopathic Products is recalling Candida Albicans homeopathic remedy due to manufacturing quality control violations. The voluntary recall affects 1,047 bottles distributed nationwide.
Product
Candida Albicans, Potency: 9C, 10C, 12C, 13C, 14C 15C 16C, 19C, 24C, 25C, 26C, 30C, 200C, 14X, 15X, 16X, 20X, 288X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1128-2022·2022-06-22
Candida Parapsilosis homeopathic remedy recalled for manufacturing practice deviations
Washington Homeopathic Products is recalling Candida Parapsilosis homeopathic remedies distributed nationwide due to manufacturing practice deviations. The recall affects 134 bottles under lot numbers 22315 and 26502.
Product
Candida Parapsilosis, Potency: 14X, 15X, 16X, 20X, 28X, 30X, 9C, 10C, 13C, 15C, 25C, 30C, 13X, 27X, 30X, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1158-2022·2022-06-22
Artri Ajo King Tablets Recalled for Unapproved Drug Claims
Walmart is recalling all lots of Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets nationwide. The product was marketed without FDA approval based on unapproved labeling claims.
Product
Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Category
Drug
Distribution
Distributed nationwide