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. 2,661 recalls have been distributed to Arkansas in the last 12 months.
Showing 2861–2880 of 49,990 recalls
Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...
The Issue: Presence of foreign substance: Presence of Benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Rising Pharma Holding, Inc....
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tolterodine Tartrate Extended-Release Capsules Recalled by The Harvard Drug...
The Issue: Failed Dissolution Specifications: Out of specification results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations: Nitrosamine Drug...
The Issue: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: InPen smart insulin pen Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pens may have been incorrectly assembled therefore users could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...
The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...
The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...
The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...
The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...
The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...
The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimulation RC Clinician Programmer Application Recalled by Medtronic...
The Issue: There is a software issue that can permanently disable communication with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Recalled by Cordis US Corp Due to product mix-up; Vascular stent...
The Issue: product mix-up; Vascular stent labeled as one size but contains a different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Recalled by Cordis US Corp Due to product mix-up; Vascular stent...
The Issue: product mix-up; Vascular stent labeled as one size but contains a different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.