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. 2,576 recalls have been distributed to Michigan in the last 12 months.
Showing 22841–22860 of 53,342 recalls
Recalled Item: AXIOM Artis MP Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis TC Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dFC Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL AED PRO Automated External Defibrillator Product Usage: The AED...
The Issue: There is a potential for the device to fail to deliver energy to the patient.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Assayed Multi-Sera Level 2 Recalled by Randox Laboratories, Limited...
The Issue: The RX Series control target and range value for ALT (Tris buffer without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci -series System Control¿Module Recalled by Abbott Gmbh & Co. KG...
The Issue: Abbott has identified an issue with all on market versions (v2.6.0 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luer Lock Set - Catalog # MPC-125 Recalled by Molded Products Inc Due to...
The Issue: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to An...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to An...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only)...
The Issue: Lack of an adequate sterilization validation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only)...
The Issue: Lack of an adequate sterilization validation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm...
The Issue: WM-NP/DP2 workstations could become unstable and may fall over if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone HCl in 0.9% sodium chloride Recalled by PharMEDium Services,...
The Issue: Incorrect Product Formulation; Firm's customer resource center (CRC)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myorisan (isotretinoin capsules Recalled by Akorn Inc Due to Labeling: Label...
The Issue: Labeling: Label mix-up: Product secondary carton erroneously states 40mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PTS Panels Lipid Panel test strip: IVD Lipid Panel Test Recalled by Polymer...
The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Panels Lipid Panel test strip: IVD Lipid Panel Recalled by...
The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Overlap Vest Recalled by Burlington Medical, LLC Due to The protective...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vest Recalled by Burlington Medical, LLC Due to The protective material used...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.