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. 1,975 recalls have been distributed to Arkansas in the last 12 months.
Showing 15521–15540 of 49,990 recalls
Recalled Item: Logical cup liner - Product Usage: intended to replace a Recalled by...
The Issue: Product mislabeled, with the incorrect product inside the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Interlock Suspension System Lanyard Body: An external prosthetic...
The Issue: the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guan's Enoki Mushroom - Champigons d'enoki Recalled by Forest Mushroom Food...
The Issue: Michigan Department of Agriculture and Rural Development sampled Enoki...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD ChloraPrep Hi-Lite Orange 26 mL Applicator (2% w/v chlorhexidine Recalled...
The Issue: Defective Delivery System: An increase in complaints identified endcap being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Evrysdi (risdiplam) for oral solution Recalled by Genentech Inc Due to...
The Issue: Defective Container: complaints received regarding some incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asenapine Sublingual Tablets Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Incorrect Product Formulation; product was manufactured with the incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asenapine Sublingual Tablets Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Incorrect Product Formulation; product was manufactured with the incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Econocare Plus Waffle Overlay- Intended for use as a medical Recalled by...
The Issue: Product contamination-a trace amount of dried bodily fluids may expose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Enterprise Viewer - Product Usage: intended to be Recalled...
The Issue: A software defect was identified where the Image Styles defined by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 3 (GTIN 00840682147378) Recalled by GE Healthcare,...
The Issue: The IGS system can experience a single vertical line defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Cardiac Assessment System for Exercise Testing and CardioSoft...
The Issue: If a certain sequence of events occur, the pdf test report that belongs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU Recalled by...
The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer....
The Issue: Instruments were assembled and serviced using a defective lot of tubing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...
The Issue: Impacted lot may leak inside the ARIES instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Penumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Elevated rates of false positive/false negative and control failures while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13...
The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.