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. 2,428 recalls have been distributed to Michigan in the last 12 months.
Showing 47861–47880 of 53,342 recalls
Recalled Item: Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile Recalled...
The Issue: Issues with the Ingenuity TF PET/CT Software Version 4.0 could pose a risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND Safety Introducer with Extended Dwell Catheter Recalled by Access...
The Issue: Access Scientific is recalling the POWERWAND Saftey Introducer with Extended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buurma Farms Cilantro Recalled by Buurma Farms Inc Due to Potential Listeria...
The Issue: The firm was notified by one of their customers of a positive Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Harmony Equipment Management System Recalled by Steris Corporation Due to...
The Issue: Dr¿ger Medical GmbH has notified STERIS of the potential for a break in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: The manufacturer has conducted a review of the results of product testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO - Beam shaping block for Radiation Therapy. Recalled by Elekta,...
The Issue: Clinical mistreatment may occur when there are errors in the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particulate embedded in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride 2% and Epinephrine 1:100 Recalled by Novocol...
The Issue: Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEART CATH CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH TRAY Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.