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. 2,662 recalls have been distributed to Arkansas in the last 12 months.
Showing 1021–1040 of 49,990 recalls
Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: an out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: an out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CentriMag Blood Pump Recalled by Thoratec LLC Due to Acute circulatory...
The Issue: Acute circulatory support system pump may not fit into the motor and reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kit Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia circuit kit Recalled by Medline Industries, LP Due to Firm...
The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine Hydrochloride Recalled by STAQ Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % Recalled by USV...
The Issue: Failed Impurities/Degradation Specifications: The result for 'Any individual...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sucralfate Tablets Recalled by Amerisource Health Services LLC Due to CGMP...
The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 on September 30,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCL PF Recalled by STAQ Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL Citrate PF Recalled by STAQ Pharma, Inc. Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...
The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.