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. 939 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
939 in last 12 months

Showing 44141–44160 of 53,342 recalls

Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2014· Frito-Lay, Inc

Recalled Item: Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package Recalled by...

The Issue: Printing error by the packaging manufacturer erroneously added a "GF" symbol...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2014· Alexion Pharmaceuticals, Inc.

Recalled Item: Soliris (eculizumab) Recalled by Alexion Pharmaceuticals, Inc. Due to...

The Issue: Presence of Particulate Matter: Product failed the appearance for the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Carestream Health Inc.

Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...

The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...

The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...

The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...

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

Class III — Low RiskOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Synthes, Inc.

Recalled Item: Synthes Guide Blocks for the 2 Column Plate 6 Hole Recalled by Synthes, Inc....

The Issue: The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2014· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an oncology information system used to manage Recalled by...

The Issue: MOSAIQ does not re-calculate the agent volume when the user changes the...

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

Class II — Potential Health HazardOngoing