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. 2,564 recalls have been distributed to Michigan in the last 12 months.
Showing 17561–17580 of 29,286 recalls
Recalled Item: FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous...
The Issue: A specific lot of the FlexFlowTM Venous Cannula, 200-200, is being recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Recalled...
The Issue: There have been reported incidents of fluid leaks at the luer connection....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Mobius Imaging, LLC Due to If the...
The Issue: If the tilt-drive motor has an intermittent connection or broken encoder or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System...
The Issue: A faulty footswitch may result in unintended ultrasonic fragmentation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Recalled...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer....
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prevent G Safety Winged Blood Collection Set Glide - Rx Recalled by...
The Issue: Complain due to the hub needle came out when the nurse draw the blood and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier III in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic...
The Issue: This product is not meeting the current storage labeling for unopened VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015) Recalled by...
The Issue: Product was placed into distribution prior to completion of all required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda(R) Intrathecal Catheter Recalled by Medtronic...
The Issue: There is a possibility that specific lots of catheters that have recently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GastriSail" Gastric Positioning Device Product Usage: The GastriSail gastric...
The Issue: Reports of gastric or esophageal perforation occurring in procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...
The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.