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. 2,520 recalls have been distributed to Michigan in the last 12 months.
Showing 23381–23400 of 29,286 recalls
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedecal SA Mobile Diagnost w DR x-ray system Recalled by Sedecal USA, Inc....
The Issue: Due to a software defect, the system may sporadically apply the default x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...
The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Catheter / Cholangiogram Catheter 9100 Series. Recalled by American...
The Issue: Catheters were not sealed before sterilization. and was not detected through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...
The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...
The Issue: A drop in staining intensity over time has been observed. These lots may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity Core Computed Tomography X-ray Systems....
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems...
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity Core 128 Computed Tomography X-ray...
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific autoHDL Reagent H7545 H7545-R1 in a bulk cube Recalled by...
The Issue: Crystals may be observed in the R1 reagent. Crystals may be a result of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pluer-evac Sahara Chest Drainage System Recalled by Teleflex Medical Due to...
The Issue: Package contains incorrect sized unit: The adult sized S-1100-08LF product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuclear Gamma Cameras (ADAC Vertex Classic Recalled by Philips Medical...
The Issue: During clinical use of a Vertex Plus Gamma Camera, as the detector heads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Vital Signs LightWand Stylet. A device inserted into an Recalled...
The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introduction Pack. A device inserted into an endotracheal tube to Recalled...
The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...
The Issue: Multiaxial screws may not meet internal requirements related to fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.