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. 2,716 recalls have been distributed to Michigan in the last 12 months.
Showing 5761–5780 of 29,286 recalls
Recalled Item: Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA Recalled by Smiths Medical ASD...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PNVMNIB21 Recalled by Cardinal...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Portacath Pack Recalled by Cardinal Health...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion PLUNGER FLOAT PLATE Recalled by Smiths Medical ASD Inc. Due to A...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PG33BTO21 Recalled by Cardinal...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel TODD HEWITT W. CNA (LIM BROTH) Recalled by Remel, Inc Due to On lot of...
The Issue: On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to One lot of KWIK STIK ANA (3...
The Issue: One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software update corrected an issue where "low" and "terminal" battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...
The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...
The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Functional MR V1.0 Recalled by OLEA MEDICAL Due to When exporting regions of...
The Issue: When exporting regions of interest in DICOM SEGMENTATION format, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit -...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran Endobronchial: Models: INS-5925 SPiN Access Catheter¿ 180 Degree for...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard...
The Issue: Diameter mismatch between coaxial and biopsy needle (cutting cannula) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Epiphany Cardio Server E3 ECG Management System Servers with Recalled...
The Issue: Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow ErgoPack Pressure Injectable One-Lumen PICC Recalled by ARROW...
The Issue: This recall has been initiated due to reports that the product code and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.