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. 2,632 recalls have been distributed to Michigan in the last 12 months.
Showing 19061–19080 of 53,342 recalls
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nabumetone Tablets Recalled by American Health Packaging Due to Labeling Not...
The Issue: Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expansion Control Overlay Recalled by EHOB, Inc. Due to QC inspection...
The Issue: QC inspection observed that a portion of the lot may have been contaminated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista one-piece hydrophobic acrylic toric intraocular lens Recalled by...
The Issue: The toric axis marks were misaligned (from the expected position in relation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.8mm Truss Wire Recalled by New Standard Device Inc Due to 1.8mm truss...
The Issue: 1.8mm truss wires are being removed to facilitate the introduction of 2.0mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACTIV.A.C Therapy System Recalled by KCI USA, INC. Due to The device may...
The Issue: The device may power off without notification to the user resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips M3015A Microstream CO2 Extension Model No. 862393 -used with...
The Issue: Affected M3015A extensions are incompatible with the lntelliVue X3 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lokomat Pro Recalled by Hocoma AG Due to The motor controller may fail,...
The Issue: The motor controller may fail, which can potentially lead to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.