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. 1,053 recalls have been distributed to Arkansas in the last 12 months.
Showing 16001–16020 of 49,990 recalls
Recalled Item: Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed...
The Issue: SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Radiological Image Processing System - Product Usage:...
The Issue: The wrong patient information may be displayed in the viewer or PowerJacket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS XP System: Multipurpose system for in vitro coagulation studies....
The Issue: Siemens Healthcare Diagnostics Products GmbH has confirmed that the BCS XP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Recalled by...
The Issue: Due to Products being incorrect labeling "for diagnostic use" and labelled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consist of a distal connection mechanism (either standard Terumo Ball...
The Issue: There is a potential for the stainless steel locking plates on the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen Recalled by A-S Medication Solutions LLC. Due to Labeling:...
The Issue: Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Menopur 75 IU Recalled by Ferring Pharmaceuticals Inc Due to Failed pH...
The Issue: Failed pH specifications: Out of Specification pH results for 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wilton Holiday Mix Sprinkles Recalled by Wilton Industries Inc Due to...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Holiday Home Assorted Treat Toppings Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Autumn Assorted Treat Toppings Sprinkles Recalled by Wilton...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Valentine Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilton Rainbow Chip Crunch Sprinkles Recalled by Wilton Industries Inc Due...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...
The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyWay Walker Chassis - Product Usage: is intended for use Recalled by James...
The Issue: Due to a failure of the welds, the casters detached from the rear legs of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cellex qSARS-Cov-2 Antigen Rapid Test Recalled by Cellex Due to The kit does...
The Issue: The kit does not have an emergency use authorization (EUA).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic (Medical Charged-Particle Radiation Therapy System)....
The Issue: In case of a failed automatic marker detection, a software error causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to...
The Issue: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.