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. 2,532 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,532 in last 12 months

Showing 2866128680 of 53,342 recalls

Medical DeviceDecember 4, 2017· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...

The Issue: Distribution of medical devices with unapproved green LED light used to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Smiths Medical ASD Inc.

Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...

The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2017· Accord Media, LLC

Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...

The Issue: Distribution of medical devices with unapproved green LED light used to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2017· ProSun International, LLC

Recalled Item: Sundream 12 V tanning bed Recalled by ProSun International, LLC Due to The...

The Issue: The 30 minute maximum tanning time has been reduced to 20 minutes.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2017· Fresenius Vial Sa

Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...

The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Elekta, Inc.

Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...

The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Mako Surgical Corporation

Recalled Item: RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee...

The Issue: Incorrect product and/or label. Sizing is labeled incorrectly.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...

The Issue: The firm made multiple changes to the product requiring the submission of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 1, 2017· Ohmeda Medical

Recalled Item: Rotating IV Pole Rotating IV Pole falls under the category Recalled by...

The Issue: There is the potential for the Rotating IV Pole to fall. A fall could result...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 30, 2017· BYL Solutions Inc.

Recalled Item: Bull Capsules Recalled by BYL Solutions Inc. Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA; product found to be tainted with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

Recalled Item: All sterile drug preparations remaining within expiry prepared from...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

Recalled Item: All sterile drug preparations remaining within expiry prepared from Morphine...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

Recalled Item: All sterile drug preparations remaining within expiry prepared from Fentanyl...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

Recalled Item: All sterile drug preparations remaining within expiry prepared from...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 29, 2017· Prinston Pharmaceutical Inc

Recalled Item: Valsartan Tablets Recalled by Prinston Pharmaceutical Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: confirmed customer complaint of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 29, 2017· Blue Fusion Natural

Recalled Item: BLUE PEARL capsules Recalled by Blue Fusion Natural Due to Undeclared Sildenafil

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LPS-FLEX GSF OPT SZ C-L¿ LPS-FLEX GSF OPT SZ C-R¿ Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing