Access Scientific recalls BD PosiFlush SF Saline Flush Syringes with packaging holes that could compromise sterility. Affected units include specific lot numbers for POWERWAND ED Quick Kit 3FR 6cm. Stop using immediately to prevent infection risks.
Saline Flush Syringe compromised sterility due to holes in the packaging.
Access Scientific recalls BD PosiFlush SF Saline Flush Syringes used in POWERWAND ED Quick Kit 3FR 6cm. The syringes have packaging holes that could compromise sterility, risking infection if used for medical procedures.
The syringe packaging has holes that could allow contaminants to enter the sterile product. This compromises sterility, meaning the syringe might not be safe for medical use and could cause infections if used for blood sampling or intravenous fluid administration.
Users of the BD PosiFlush SF Saline Flush Syringe 10mL in POWERWAND ED Quick Kit 3FR 6cm are affected. Healthcare professionals and patients using this syringe for blood sampling or intravenous fluid administration are at highest risk.
Check for the lot numbers: 257828, 258294, 259262, 260814, 260173, 261861, 264561, 266804, 266805, 267191, 269121. The syringe is part of the POWERWAND ED Quick Kit 3FR 6cm product line.
Discard the syringe if you have the affected lot numbers listed above to prevent potential contamination.
The syringe packaging has holes that could compromise sterility, risking infection if used for medical procedures.
Lot numbers 257828, 258294, 259262, 260814, 260173, 261861, 264561, 266804, 266805, 267191, and 269121.
The recall record does not mention any remedy or replacement options.
We’ve drafted a message you can send Access Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1972-2020 — Access Scientific Access Scientific Hello, I own a Access Scientific that is covered by recall Z-1972-2020 from Access Scientific. 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.
