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 26701–26720 of 28,355 recalls
Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health hCG Cassette Rapid Test Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego Inc. is recalling the Cardinal Health hCG Cassette Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee systems x-ray Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The firm became aware of a potential issue with Artis zee systems bearing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medium 2-Hooks Spreader Bar for use with Loop Slings Recalled by Arjo, Inc....
The Issue: The upper portion of the hooks on the spreader bar are too flexible for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifeguard Infusion Set with Smartsite Recalled by Churchill Medical Systems,...
The Issue: The label on the device states that the item number is CLGY-2210 when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantx Recalled by GE Healthcare, LLC Due to A locking nut...
The Issue: A locking nut might loosen out of the overhead Video Monitor Suspension yoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chenica Gunnell Rehab Series of Wheelchairs (GRSW) Recalled by CHENICA INC....
The Issue: The wheelchairs may not meet the specifications of WC-19 (crash testing),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Bipolar Generator Foot Pedal Recalled by Aesculap, Inc. Due to The...
The Issue: The bipolar energy did not stop after release of the foot pedal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Recalled by St Jude Medical Inc Due to The distal end of...
The Issue: The distal end of the core wire of the TorqVue FX Delivery System could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Recalled by Elekta, Inc. Due to If the Apex collimator is incorrectly...
The Issue: If the Apex collimator is incorrectly installed on the radiation head, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK INSIGHT DENTAL FILM in SureSoft Packets Recalled by Carestream Health,...
The Issue: Missing symbols and manufacturing information on the clear carton label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SybronEndo Elements Obturation Unit Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SybronEndo Replacement AC Power Cord Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...
The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic Recalled by Philips Healthcare Inc. Due...
The Issue: An inspection shows several IATDs (Installation Acceptance Test could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage:...
The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Catalog Number:283905000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs BleaseSirius Anesthesia Workstation Recalled by Del Mar Reynolds...
The Issue: A defect in CAS I/II Absorbers in the Spacelabs Anesthesia Workstations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.