Resource Optimization & Innovation LLC recalls Regard SRHS Central Line Kit (Sterile, 20/case) due to potential packaging holes that could compromise sterile fields. Affected lot numbers include 257967, 259035, and others.
There is a potential for the product to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
Resource Optimization & Innovation LLC is recalling Regard SRHS Central Line Kit sterile syringes because the packaging might develop holes, risking contamination of the sterile field. This could lead to infections if the syringes are used without proper sterility.
The packaging may develop holes, which could compromise the sterile field. If the syringes are not properly sealed, they might become contaminated, increasing the risk of infection during medical procedures.
Healthcare professionals using the Regard SRHS Central Line Kit for vascular access devices are most at risk, particularly those handling the sterile syringes in clinical settings.
Check for lot numbers: 257967, 259035, 259418, 260742, 261252, 261888, 263836, 264669, 268918, 271005, 265730, 270198, and 270567 on the packaging. The product is a sterile saline flush syringe kit for vascular access devices.
Inspect the packaging for holes or damage that could compromise sterility.
The packaging may develop holes, which could compromise the sterile field and lead to contamination.
Lot numbers 257967, 259035, 259418, 260742, 261252, 261888, 263836, 264669, 268918, 271005, 265730, 270198, and 270567.
The recall does not require immediate discontinuation; check for packaging holes before use.
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-2369-2020 — Resource Optimization & Innovation LLC Resource Optimization & Innovation LLC Hello, I own a Resource Optimization & Innovation LLC that is covered by recall Z-2369-2020 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.
