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 26921–26940 of 28,355 recalls
Recalled Item: Medtronic Intersept Custom Tubing Pack with or without coating ( Recalled by...
The Issue: Medtronic is initiating an Urgent Medical Device Customer Notification. We...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher & Paykel Healthcare reusable breathing circuit. Non-heated breathing...
The Issue: FPH has become aware that one batch of tubes supplied to FPH may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable...
The Issue: Zimmer is initiating a lot specific recall because affected lots could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Circuit used with the Life Pulse High Frequency Ventilator. Recalled...
The Issue: Customer complaints received indicate the heater wire insulation can melt,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COONMAD/MORREY TOTAL ELBOW ELBOW COMPONENT REPLACEMENT SET BUSHINGS & PINS...
The Issue: Zimmer is initiating a lot specific recall because affected lots could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoTac Delivery Handle Recalled by BioHorizons Implant Systems Inc Due to...
The Issue: The cleaning instructions provided may not be sufficient to remove residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche COBAS INTEGRA 400 and 400 plus Analyzer Recalled by Roche Diagnostics...
The Issue: A software security issue with Oracles TNS-Listener component has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium Tack Starter Kit Recalled by BioHorizons Implant Systems Inc Due to...
The Issue: The cleaning instructions provided may not be sufficient to remove residual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Praxair Vantage Grab n Go - Gas Cylinder pressure regulator Recalled by...
The Issue: Isolated incidents of ignition inside Grab n' Go cylinders that had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek 11 MM Fully Fluted Reamer Recalled by DePuy Mitek, Inc., a...
The Issue: Specific units of the DePuy Mitek Sterile Reamers are not labeled correctly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 9000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phenobarbital Recalled by Abbott Laboratories, Inc Due to...
The Issue: Abbott Diagnostics is recalling Clinical Chemistry Phenobarbital reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 8000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...
The Issue: There is a potential for data loss associated with empty path names...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity PACS Workstation Recalled by GE Healthcare It Due to While...
The Issue: While merging exams in a test instance, merges carry forward in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viterion TeleHealth Monitor Model Number V100 Recalled by Viterion...
The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Offset Tibial Tray 2.5 mm Adaptor Recalled by Biomet, Inc. Due to...
The Issue: Biomet investigation identified that the square end of the offset tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEG NeuroAmp Recalled by EEG Info Due to Mislabeling
The Issue: EEG Info, Inc. is recalling the EEG Neuroamp device because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viterion TeleHealth Monitor Model Number V100-BGM Recalled by Viterion...
The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viterion TeleHealth Monitor Model Number V500 Recalled by Viterion...
The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.