Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,700 recalls have been distributed to Louisiana in the last 12 months.
Showing 4361–4380 of 29,201 recalls
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 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 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: 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: Alinity m System Recalled by Abbott Molecular, Inc. Due to The Alinity m...
The Issue: The Alinity m System camera detects whether tubes are "capped." If the...
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: 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 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.
Recalled Item: Trilogy Evo 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: LifeVentEVO2 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: Aeris EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...
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 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: Garbin EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...
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: GE Healthcare Innova IGS 6 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.