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. 2,576 recalls have been distributed to Michigan in the last 12 months.
Showing 22001–22020 of 53,342 recalls
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Jarit GEMINI CLAMP 9 1/4 inch - used in Recalled by Integra...
The Issue: A small crack at the box lock corner may after multiple cleaning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...
The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...
The Issue: The device data being collected and transferred to the monitoring center may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Recalled...
The Issue: Possible presence of small plastic pieces caused by a manufacturing failure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...
The Issue: A complaint was received regarding kinking of the device prior to use. If a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...
The Issue: The electrode lead connector has a protruding conductor beyond insulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...
The Issue: The mounts on the monitor may have an insufficient weld.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder...
The Issue: Separation of front and rear barrels upon activation of the safety feature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 Nerve Monitor Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker C2 NerveMonitor's design and instructions may not optimally address...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.