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. 2,457 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,457 in last 12 months

Showing 2592125940 of 28,748 recalls

Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Straight Recalled by Smith & Nephew, Inc....

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture Recalled...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture Recalled...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith &...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...

The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company - Health Care Business

Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...

The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Medicel Ag

Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...

The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...

The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...

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

Class II — Potential Health HazardOngoing