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. 2,722 recalls have been distributed to Michigan in the last 12 months.
Showing 4701–4720 of 29,286 recalls
Recalled Item: Masimo Rad-G Recalled by Masimo Corporation Due to Their is a potential that...
The Issue: Their is a potential that Oximeter may automatically power off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Rad Recalled by Bio-Rad Laboratories Due to Due to incorrect...
The Issue: Due to incorrect calibrations and controls, their is a potential of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signia" Small Diameter Curved Tip Intelligent Reload Recalled by Covidien,...
The Issue: Under certain firing conditions, reloads were found to articulate in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload Recalled by...
The Issue: Under certain firing conditions, reloads were found to articulate in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cystatin C Calibrator - In vitro diagnostic (IVD) use in Recalled by Randox...
The Issue: Cystatin C Calibrator Series CVS 2699, is running with a negative bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Boot Assembly Recalled by Baxter Healthcare Corporation Due to Three...
The Issue: Three lots of the Boot Assembly, Traction Device are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator): Type/Catalog: SAM...
The Issue: Automated external defibrillators were shipped in their test configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a Recalled...
The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW QuickFlash Radial Artery Catherization (wire Recalled by ARROW...
The Issue: Teleflex is initiating this voluntary recall for the above-mentioned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Nasal Intubation Kit with 6mm Endotrol Tube-To perform a Recalled...
The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assembly Recalled by Think Surgical, Inc. Due to There is a galling effect...
The Issue: There is a galling effect (cold-weld) caused by friction between the array...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preat Nobel Active/Conical-compatible RP Titanium Blank Recalled by Preat...
The Issue: Due to a manufacturing issue, the screw seat location on the abutment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: UNclog Eye Mask Product Name: UNclog Eye Mask Recalled by EYE...
The Issue: Due to a change in the safety clips for the heated eye masks, the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Total T4 Recalled by Beckman Coulter, Inc. Due to Four lots of Access...
The Issue: Four lots of Access Total T4 reagent lots demonstrated imprecision outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microStar Reader Recalled by Landauer Due to Permanent discontinuance of the...
The Issue: Permanent discontinuance of the microSTARii medical dosimetry system....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK Non-DEHP Solution Set Luer Lock Adapter Recalled by Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software versions 5.14 and earlier used in Recalled by Life...
The Issue: Torrent Suite Dx Software versions 5.14 and earlier used in connection with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Substrate Recalled by Beckman Coulter, Inc. Due to On 07 February...
The Issue: On 07 February 2024 Beckman Coulter made the decision to conduct a field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENSIVE Conductive Adhesive Gel Recalled by Natus Neurology Inc Due to Natus...
The Issue: Natus has become aware that its third-party supplier Parker Laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP...
The Issue: When a paraPAC plus ventilator is switched to the operating mode of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.