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 26581–26600 of 28,355 recalls
Recalled Item: U2 Acetabular cup Recalled by Orthopedic Alliance LLC Due to The recall of...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zweimueller Type Stem SCS-Standard Sz 01 Zweimueller Type Stem SCS-Standard...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50 mm Screw Recalled by Spinal Solutions, LLC Due to The recall of the...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 50 mm Rod Recalled by Spinal Solutions, LLC Due to The recall of the Loaner...
The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.75mm x 12mm Fixed Cervical Screws. Components of the Genesys Recalled by...
The Issue: Manufacturing residue may be present on the cervical screws. Use of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DPL Single Stage Venous Cannula with Metal Tip Recalled by...
The Issue: Potential for uncharacteristically rough metal edges to occur along the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel X/pect Flu A&B Control Swabs Recalled by Remel Inc Due to Flu A+...
The Issue: Flu A+ Control Swabs incorrectly give Flu A- results when used for quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tecan Freedom EVO with Touch Tools Suite Version 3.0 The Recalled by Tecan...
The Issue: WIth TouchTools 3.0 after the execution of a Rich User Prompt in Display and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helion S Exam Light or H300 The device is intended Recalled by Trumpf...
The Issue: Possible fatigue failure of the plastic joint may occur after an average use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...
The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...
The Issue: It was reported from a complaint that study category labels of "Prior" and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...
The Issue: A software defect was discovered that causes images to be out of context...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 and Ingenuity Computed Tomography X-Ray Systems The Brilliance...
The Issue: This field change order is being released to update software and customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.