Product Recalls in Kentucky
Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,646 recalls have been distributed to Kentucky in the last 12 months.
Showing 5841–5860 of 28,748 recalls
Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...
The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...
The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenition 70. The device is to be used in health Recalled by Philips Medical...
The Issue: Philips has become aware of the potential for unintended radiation exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cosmedent FlexiCup Composite Finishing & Polishing System Recalled by...
The Issue: Reports were received the elastomer cup material is crumbling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: For intraventricular indications mainly used for operations within the brain...
The Issue: Trocar manufactured with the shaft too long and does not meet manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visera Hysterovideoscope Olympus HYF Type V Recalled by Olympus Corporation...
The Issue: IFU labeling is being updated to revise EtO gas mixture and elimination of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOROPTOR VRX DIGITAL SYSTEM-Digital intended for the subjective Recalled by...
The Issue: Phoroptor VRx Head may detach from the bracket that connects the Phoroptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...
The Issue: Replacement of the internal Sample Pump due to high failure rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim" XR 7 Implantable Pulse Generator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 5 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim XR 5 Implantable Pulse Genterator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...
The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System-Intended to provide fluid distension of the...
The Issue: The display of inflow volume can reach its limit of 30,000 ml during long...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.