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. 2,645 recalls have been distributed to Arkansas in the last 12 months.
Showing 3741–3760 of 49,990 recalls
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo USA, Inc. Due to...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...
The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT Recalled by...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) Port Access Kit Recalled by MEDLINE...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT...
The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 6 Plus Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.