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. 2,673 recalls have been distributed to Michigan in the last 12 months.
Showing 13601–13620 of 53,342 recalls
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Aid Kits containing acetaminophen under brand names Equate (Walmart)...
The Issue: Kits contained recalled acetaminophen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Delivery Catheter System. Part of the Harmony Transcatheter...
The Issue: There is potential for the capsule bond to break during the procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars...
The Issue: Undeclared allergen - egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Recalled by DEL...
The Issue: Product being recalled due to potential metal fragment approximately 2-3mm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AccessPLUS Large Bore Hemostasis Valves Recalled by Merit Medical Systems,...
The Issue: A design change made to a hemostasis valve to improve manufacturability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access-9 Large Bore Hemostasis Valves Recalled by Merit Medical Systems,...
The Issue: A design change made to a hemostasis valve to improve manufacturability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORE-SIGHT ELITE Absolute Tissue Oximeter Recalled by Edwards Lifesciences,...
The Issue: The StO2 values may be inaccurately low when using either the FORE-SIGHT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORE-SIGHT ELITE Tissue Oximeter module Recalled by Edwards Lifesciences,...
The Issue: The StO2 values may be inaccurately low when using either the FORE-SIGHT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALIPERIDONE EXTENDED-RELEASE TABLETS Recalled by The Harvard Drug Group Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NanoSight LM10 fitted with LM12 module. A laboratory instrument for Recalled...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoSight LM10 fitted with LM14 module. A laboratory instrument for Recalled...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL Recalled by Medtronic...
The Issue: There is a software anomaly with the InterStim X Clinician software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V680 Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Universal Flexible Arm part number Recalled by Integra LifeSciences...
The Issue: Excess force used to tighten the Universal Flexible Arm can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical, Inc. Due to...
The Issue: Lack of sterility assurance: leaking bags
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.