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. 2,469 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,469 in last 12 months

Showing 2296122980 of 28,748 recalls

Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NOBELREPLACE Tapered Groovy RP 4.3x8mm Recalled by Nobel Biocare Usa Llc Due...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC PMC RP 4.3x10mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving MRI...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC RP 5.0x13mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC RP 5.0x8mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: Replace Select Tapered TiU NP 3.5x10mm Recalled by Nobel Biocare Usa Llc Due...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC RP 4.3x13mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: NobelReplace CC PMC RP 5.0x10mm Recalled by Nobel Biocare Usa Llc Due to A...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Nobel Biocare Usa Llc

Recalled Item: Replace Select Tapered TiU NP 3.5x11.5mm Recalled by Nobel Biocare Usa Llc...

The Issue: A material used in the packaging of the dental implants may impart a sticky...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a Recalled...

The Issue: Fujifilm is reporting a corrective action due to an FDA inspection.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product...

The Issue: Fujifilm is conducting a corrective action due to an FDA inspection.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte-JetStream AZ (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 40 - Slices (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF PET/CT 16 Slice (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Diamond Select Brilliance CT 16 (Uninterruptible Power Supply (UPS)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: AXIS (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing