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. 2,617 recalls have been distributed to Arkansas in the last 12 months.
Showing 11161–11180 of 49,990 recalls
Recalled Item: Colgate Whitening Mouthwash Recalled by Family Dollar Stores, Llc. Due to...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colgate Anticavity Fluoride Toothpaste Recalled by Family Dollar Stores,...
The Issue: cGMP deviation: Product held outside of appropriate temperature storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...
The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Nephron Sc Inc Due to cGMP...
The Issue: cGMP Deviations: deviations leading to potential cross-contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-0.125% Bupivacaine HCl Injection Recalled by Nephron Sterile Compounding...
The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trisodium Citrate 0.5% Solution Recalled by Nephron Sterile Compounding...
The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog Recalled by...
The Issue: OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verify SixCess Challenge Pack. Used to confirm that critical parameters...
The Issue: Product contains incorrect chemical indicators in packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Early Bird Bleed Monitoring System Introducer Sheath Set Recalled by...
The Issue: Bleed monitoring system device design error, causing the device to not power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...
The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...
The Issue: Firm noted an increase in customer reports of leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: Burns of varying degrees can occur to patients with electrodes left in while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...
The Issue: Identification of an unknown impurity at the 12-month stability point....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...
The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.