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. 2,698 recalls have been distributed to Michigan in the last 12 months.
Showing 7961–7980 of 29,286 recalls
Recalled Item: HeartWare Ventricular Assist Device (HVAD) System Batteries Recalled by...
The Issue: Battery performance issues. Battery electrical faults render it unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use Recalled by...
The Issue: Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Bag Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Vial Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C6 Intensive Care Ventilator Recalled by Hamilton Medical AG Due to...
The Issue: Ventilator status indicator board can become loose, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation...
The Issue: The device may potentially cause a fire, leading to a safety risk.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right Recalled by Smith &...
The Issue: The product was mispackaged (swapped). The devices within the inner tray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Recalled by Neotract Inc Due to There is the potential that...
The Issue: There is the potential that during implant deployment, the device may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sprinter OTW Recalled by Medtronic Inc Due to Luer has balloon...
The Issue: Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 2.3mm Tapered Router Recalled by Stryker Instruments Due to There is...
The Issue: There is a potential for the core diameter to be undersized, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEISS Axio Observer 5 microscope Recalled by Zeiss, Carl Inc Due to An...
The Issue: An incorrect Unique Device Identification (UDI) label was installed on some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier magnetic resonance scanner Recalled by GE Healthcare, LLC Due...
The Issue: Under rare conditions, SIGNA Premier gradient coils could result in elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress Recalled by...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 40" Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 36" Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambra PACS Recalled by DICOM Grid, Inc. d/b/a Ambra Health Due to A race...
The Issue: A race condition between the storage system and services database has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.