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. 1,088 recalls have been distributed to Michigan in the last 12 months.
Showing 11541–11560 of 53,342 recalls
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ampicillin for Injection Recalled by Viatris Inc Due to Presence of...
The Issue: Presence of Particulate Matter: A complaint was received for the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride...
The Issue: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Standard Starburst Recalled by Baxter Healthcare Corporation Due to...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Advance Table Recalled by Baxter Healthcare Corporation Due to the...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Life Assist Beach Chair Recalled by Baxter Healthcare Corporation Due...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Polar Head Positnr-Device Only Recalled by Baxter Healthcare...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beach Chair Clamp Recalled by Baxter Healthcare Corporation Due to the...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simple Clamp Recalled by Baxter Healthcare Corporation Due to the adhesive,...
The Issue: the adhesive, applied to screws and bolts as an additional holding force,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...
The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 125 series iGO2 Portable Oxygen Concentrator-indicated for the...
The Issue: An unapproved adhesive used to manufacture the accumulator tank sub assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...
The Issue: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.