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. 2,666 recalls have been distributed to Michigan in the last 12 months.
Showing 14161–14180 of 53,342 recalls
Recalled Item: Rugby Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Fex D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddys Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid Pharmacy Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kroger Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Optima Coil System consists of an implantable embolization coil Recalled...
The Issue: Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRA SURFIX ALPHA Screwdriver Torx 10 Recalled by Smith & Nephew, Inc....
The Issue: The affected screwdrivers are out of specification and may not mate with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCareManager version 4.2.1 Recalled by Philips North America Llc Due to...
The Issue: eCareManager (eCM) Sentry Score software not approved for use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY Recalled by Immuno-Mycologics, Inc...
The Issue: The firm found immunoassay products used to detect cryptococcal antigen in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets Recalled by Rubicon Research Private Limited Due...
The Issue: Complaint received of foreign matter (metal) embedded in tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RayStation/RayPlan- designed for treatment planning and analysis of...
The Issue: If a new primary image set is selected while the cine loop is running, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exeter V40 Cemented Hip (150mm) Stem Recalled by Howmedica Osteonics Corp....
The Issue: There is a potential label mix between certain lots of Exeter V40 Cemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exeter V40 Cemented Hip (125mm) Stem Recalled by Howmedica Osteonics Corp....
The Issue: There is a potential label mix between certain lots of Exeter V40 Cemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pioglitazone Tablets USP Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Superpotent and Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefixime 400 mg capsule Recalled by RemedyRepack Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes Recalled by MEDLINE...
The Issue: Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR Titan OFW - MTB - Right - 1.0mm Recalled by Stryker Leibinger GmbH &...
The Issue: Inside the packaging of one reported item a non-conforming product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X060-0270 Recalled by XTANT Medical Due to The proximal opening of the...
The Issue: The proximal opening of the inserts exhibit an out of specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion Pumps Recalled by Baxter Healthcare Corporation...
The Issue: There is the potential for reduced or non-delivery of medication, in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.