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. 2,063 recalls have been distributed to Kentucky in the last 12 months.
Showing 4361–4380 of 28,748 recalls
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion Pump Recalled by Baxter Healthcare Corporation...
The Issue: One device was improperly performed testing prior to release from a Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Surgical Tape Recalled by 3M Company - Health Care Business Due...
The Issue: Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP Distal Lateral Fibular Plate Recalled by Zimmer, Inc. Due to Thread...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24K Premium Lense Recalled by Ontact Inc Due to Contact lenses recalled due...
The Issue: Contact lenses recalled due to potential bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...
The Issue: Nail system contains an out of specification driver-socket which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...
The Issue: Nail system contains an out of specification driver-socket which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Potential for...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Potential for...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.