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. 2,591 recalls have been distributed to Arkansas in the last 12 months.
Showing 15101–15120 of 49,990 recalls
Recalled Item: Solifenacin Succinate Tablets Recalled by CIPLA Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arjo Citadel beds originally assembled with the IndiGo modules during...
The Issue: The IndiGo power cord might wear during use which could lead to its damage,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for 15%...
The Issue: There is a potential for 15% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D Imaging Recalled by GE OEC Medical Systems, Inc Due to There is a...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Recalled by...
The Issue: Due to a design issue, inflation syringe handle separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite mobile C-arm - Product Usage: intended to provide Recalled by GE...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lingen SAMPLE Disposable Virus Sampling Kit pack Recalled by Mercedes...
The Issue: No 510(k) clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lingen Disposable Virus Sampling Kit Recalled by Mercedes Medical, Inc. Due...
The Issue: No 510(k) clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chantix (varenicline) tablets Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chantix (varenicline)Tablets Recalled by Pfizer Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDAs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xolair (omalizumab) Injection Recalled by Genentech Inc Due to Failed...
The Issue: Failed Stability Specifications: Out of Specification results of Polysorbate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation...
The Issue: Expired adhesive used as an electrical insulation barrier and as a secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmer with Attachment Tab Recalled by Cardinal Health 200, LLC...
The Issue: A caution statement is being added to remind the user to activate away from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmer without Attachment Tab Recalled by Cardinal Health 200,...
The Issue: A caution statement is being added to remind the user to activate away from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for...
The Issue: The product in the packaging is larger (both inner and outer diameter) than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mephyton (Phytonadione) 5 mg tablets Recalled by Bausch Health Companies,...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.