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. 1,743 recalls have been distributed to Michigan in the last 12 months.
Showing 42161–42180 of 53,342 recalls
Recalled Item: Dried Bean Curd Anka Flavor 24x150g Recalled by Gemini Food Corporation Inc...
The Issue: Gemini Foods is recalling bean curd products because they may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips IntelliVue Information Center iX (release A.00 Recalled by Philips...
The Issue: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-Lipo Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...
The Issue: Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SLIM-K Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M ESPE Clinpro 5000 (1.1% Sodium Flouride) Recalled by 3M Company/3m Espe...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The XN-Series modules (XN-10 Recalled by Sysmex Corporation Due to There is...
The Issue: There is a potential for elevated hemoglobin (Hgb) and impedance platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Recalled by St Jude Medical...
The Issue: Transmitter may initiate a software reset resulting in backup operation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform...
The Issue: The devices were not shipped with the Starter Kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...
The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer Recalled...
The Issue: Chemical component of the F3 Fluid pack and environmental bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit Recalled by Reily Foods...
The Issue: Kits contain peanut and almond allergens that are not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT Recalled by Reily Foods Co....
The Issue: Kits contain peanut and almond allergens that are not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit Recalled by Reily Foods...
The Issue: Kits contain peanut and almond allergens that are not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT Recalled by...
The Issue: Kits contain peanut and almond allergens that are not declared on the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Femoral Head - indicated for hip arthroplasty for noncemented Recalled...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo (cold) Laser Desktop Control Units Recalled by Pivotal Health...
The Issue: Control units were equipped with an internal mounting kit that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...
The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...
The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.