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. 2,451 recalls have been distributed to Arkansas in the last 12 months.
Showing 26441–26460 of 28,355 recalls
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...
The Issue: The recall was initiated because Shimadzu Corporation has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....
The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...
The Issue: There was an occurrence where the patient case data did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrea CT Multi-Chamber Cardiac Functional Analysis application on Vitrea...
The Issue: Vital Images has made a decision to perform a field correction to the Vitrea...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...
The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...
The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...
The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...
The Issue: The Column rotation can accidentally be moved to a different position which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...
The Issue: Two unsealed pouches were found at an Edwards' distribution location in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...
The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rad-8 Pulse Oximeters The Rad-8 family of pulse oximeters and Recalled by...
The Issue: Masimo has identified a very small number (0.02%) of Rad-8 devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...
The Issue: This recall is being initiated because the affected lots of this product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.