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. 2,537 recalls have been distributed to Michigan in the last 12 months.
Showing 26701–26720 of 53,342 recalls
Recalled Item: AMPI Whey Powder Recalled by AMPI Due to Potential Salmonella Contamination
The Issue: Whey powder may have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...
The Issue: The product was mislabeled with the incorrect label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...
The Issue: Analyzers were distributed with software which lacks a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT systems with the SmartStep Option The system is Recalled by GE...
The Issue: On the Revolution CT systems equipped with the SmartStep Option, the Z...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET Recalled by Medical...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set Recalled by Medical...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left Recalled by...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products - Folate Reagent Pack(10758750009237)...
The Issue: The recalling firm determined that biased results may occur for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled...
The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duo-Flow Catheter Full Tray Recalled by Medical Components, Inc dba MedComp...
The Issue: The suture wings have the potential to crack or break. Potential patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922...
The Issue: The recalling firm determined that biased results may occur for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.