Product Recalls in Michigan
Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,532 recalls have been distributed to Michigan in the last 12 months.
Showing 28821–28840 of 53,342 recalls
Recalled Item: Natural Dark Chocolate Cranberries Recalled by JLM Manufacturing LLC Due to...
The Issue: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dark Chocolate Coffee Beans Recalled by JLM Manufacturing LLC Due to...
The Issue: JLM Manufacturing LLC is recalling multiple dark chocolate products due to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted & Salted Cashews and Chocolate Covered Cashews Recalled by Meijer...
The Issue: Packages are mislabeled and actually contain undeclared mixed nuts instead...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra...
The Issue: The Spectra System/Legacy Guided Surgery Handle Kit had guided handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...
The Issue: Potential for cracked luer hubs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triage Drugs of Abuse Plus TCA 25 Test Kit Recalled by Alere San Diego, Inc....
The Issue: The recalled lots have demonstrated unexpected false positive THC results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath Recalled by...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Superpotent
The Issue: Superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nexterone (amiodarone HCl) Premixed Injection Recalled by Baxter Healthcare...
The Issue: Presence of Particulate Matter:Particulate identified as polyethylene, the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.