Resource Optimization & Innovation LLC recalls Regard IV Start Kit for peripheral IV access sites due to a faulty PDI Prevantics Swab component. Affected kits include specific batch numbers and model items.
A kit component, the PDI Prevantics Swab, was recalled.
Resource Optimization & Innovation LLC is recalling their Regard IV Start Kit for preparing peripheral IV access sites because a specific swab component (PDI Prevantics Swab) is defective. This recall affects users who may have the kit with certain batch numbers, as the faulty swab could lead to improper site dressing.
The recall involves a kit component called the PDI Prevantics Swab. While the exact hazard mechanism isn't clearly described in the record, the manufacturer identified this component as defective, which could impact the safety of IV site preparation and dressing.
Healthcare professionals who use the Regard IV Start Kit for peripheral IV access sites are most at risk, particularly those with the specific batch numbers listed in the recall notice.
Check the kit's manufacturer item number (e.g., 303403REG or 303404REG) and batch numbers listed in the recall notice. The affected kits include specific batch numbers such as 272394, 272723, and others.
Identify the manufacturer item number and batch numbers on the kit to see if it matches the recalled items listed in the notice.
The manufacturer identified the PDI Prevantics Swab component as defective, but the specific hazard mechanism isn't clearly described in the recall notice.
Kits with manufacturer item numbers 303403REG, 303404REG, or 57931 and specific batch numbers listed in the recall notice.
The recall does not specify a remedy or immediate action, so there is no instruction to stop using the kit now.
We’ve drafted a message you can send Resource Optimization & Innovation LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-0950-2022 — Resource Optimization & Innovation LLC Resource Optimization & Innovation LLC Hello, I own a Resource Optimization & Innovation LLC that is covered by recall Z-0950-2022 from Resource Optimization & Innovation LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
