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. 2,463 recalls have been distributed to Michigan in the last 12 months.
Showing 43701–43720 of 53,342 recalls
Recalled Item: Array LaserLink Recalled by Lumenis, Inc. Due to Lumenis initiated a...
The Issue: Lumenis initiated a field-correction for the Array Laser Link",...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below...
The Issue: Potential issues with the ProVue driver have been identified which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED). For use in general traumatology....
The Issue: The affected Small Electric Drive (SED) may operate solely in reverse mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAM Junctional Tourniquet (SJT) Auxiliary Recalled by Sam Medical Products...
The Issue: SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ HbA1c Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Defective...
The Issue: Defective Container: Product leaks when inverted.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROPRANOLOL HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due...
The Issue: CGMP Deviations: Citations given to API supplier by the Italian Health...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McCormick Ground Oregano in 0.75 oz plastic bottle. NUMBER: Recalled by...
The Issue: Retail sample of ground oregano tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...
The Issue: An internal finding identified the presence of pinholes/cuts in some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is...
The Issue: BioFire Defense, LLC is initiating a field action for JBAIDS Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...
The Issue: Water may leak into the center gas lumen of the Patient Circuit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...
The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP Immunoassay System Recalled by Siemens Healthcare...
The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.