Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit IT1075-DUKE-HSP, IT1076-DUKE-HSP and IT1077-DUKE-HSP
FDA Recall Z-0832-2022 · Posted None
Advertisement
Recalling FirmInfuTronix LLC
Recall StatusOpen, Classified
Product CodeFRN
Date Initiated2021-10-19
Product Quantity74 units
Reason for Recall
An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H) infusion pumps in error that may impact patient safety if used on patients.
Firm Action
An IMPORTANT PRODUCT INFORMATION letter dated 10/19/21 was sent to customers.
InfuTronix LLC has recently become aware of an unreleased Version 4 Protocol Library for Duke University Hospital was installed on your Nimbus PainPro (H) infusion pumps in error that may impact patient safety if used on patients. Please ensure that all your potential customers and potential users in your facility are made aware of this notification and the recommended actions.
Product Issue
Version 4 of the Duke Protocol Library was installed on your infusion pumps in error.
Affected Product Details
Nimbus PainPro (H) Pump, Model numbers: IT1072, sold as kits IT1075-DUKE-HSP
Total number of infusion pumps affected: 3
Lot numbers involved: 2009231440
Instructions
1. Place all units you have in-house on product-hold and stop further distribution
2. Inform your customer to discontinue use of the affected infusion pumps.
Product Correction
InfuTronix will be contacting you to resolve this issue as quickly as possible.
Contact Information
Your Account Manager, Vann Griffin, email: [email protected],
phone: (919) 606-8339
Or John LaFratta, Vice President of Sales, email: john.lafratta@ nimbuspainpro.com , phone: 315-729-5564.
Please be assured that maintaining a high level of safety and quality is our highest priority. If you have any questions, please contact us immediately.
Root Cause
Employee error
Distribution Pattern
US Nationwide distribution in the states of NC and OH.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement