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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 1641–1660 of 29,286 recalls
Recalled Item: Product Name: SmartPath to Ingenia Elition X Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Ambition S Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Evolution Upgrade 1.5T Recalled by Philips North America Llc...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for XR and 3.0T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for 1.5T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: MR 5300 Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Upgrade to MR 7700 Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The HemoCue Glucose 201 Microcuvettes are designed for use with Recalled by...
The Issue: Glucose microcuvettes experienced transit time outside of limits, so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One+ Continuous Glucose Monitoring System Recalled by Dexcom, Inc....
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One Continuous Glucose Monitoring System Recalled by Dexcom, Inc. Due...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G7 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IVENIX INFUSION SYSTEM LVP Blood Products Administration Set Recalled by...
The Issue: Mis-assembly error of Blood Products Administrations Sets where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium Needle-Free Syringe: 3 mL Recalled by BD SWITZERLAND SARL Due to...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Novum IQ Syringe Pump Recalled by Baxter Healthcare Corporation Due...
The Issue: Baxter has identified a design issue which may cause the pump to detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.