Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,635 recalls have been distributed to Arkansas in the last 12 months.
Showing 6181–6200 of 49,990 recalls
Recalled Item: HONEY MANUKA BUNNY LOVE Recalled by Pyramids Wholesale Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SILVERBACK XXX POWER MALE ENHANCEMENT Recalled by Pyramids Wholesale Inc....
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The GOAT SUBLINGUAL STRIP Recalled by Pyramids Wholesale Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: libigrow RED DRAGON+ Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GoHARD 25000 Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: 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: 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: GE Healthcare Allia IGS 7 OR 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 Interact Discovery RT Recalled by GE Medical Systems, SCS Due...
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.
Recalled Item: GE Healthcare Innova IGS 5 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 7 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 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.