Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,496 recalls have been distributed to Connecticut in the last 12 months.
Showing 16661–16680 of 28,245 recalls
Recalled Item: ACE(TM) BRAND Recalled by 3M Company - Health Care Business Due to Mold was...
The Issue: Mold was found on the non-patient contact surfaces of the product and was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...
The Issue: The internal configuration of the electrometers and the Real-Time control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Mednet(TM) Medication Management Suite 6.1 and 6.21 Recalled by ICU...
The Issue: Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...
The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...
The Issue: Report was of an interrupted MR scan after patient complained about acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...
The Issue: L3 has determined in airport environments, there have been several cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...
The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fastener Recalled by Zimmer Biomet, Inc. Due to It was identified that the...
The Issue: It was identified that the product was not assembled correctly causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Extended Stem Size 2. Orthopedic implant for replacement...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Recon Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: rHead Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp. Due to...
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.