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.
Showing 22341–22360 of 29,286 recalls
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Achieve Cables Recalled by Medtronic Inc. Due to 64 units of...
The Issue: 64 units of Achieve Electrical Cables were shipped with a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...
The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...
The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...
The Issue: Inaccurate distance measurements with magnified projection X-ray images.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...
The Issue: The firm is conducting a product correction due to an increase in U90-382 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...
The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Hemoglobin A1c_3 Recalled by Siemens Healthcare Diagnostics,...
The Issue: Reagent in these lots may demonstrate an increased occurrence of high %HbA1c...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....
The Issue: Airways Development LLC has received a complaint about a canister leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Patient-Specific Surgical Guides Recalled by Materialise N.V. Due...
The Issue: Potential inaccuracies in the alignment of the guides. Surgery was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...
The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...
The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Surgical Suite II Table Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE became aware of an issue with the table transfer release mechanism of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...
The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 100 system included the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 300 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.