Access Scientific recalls BD PosiFlush SF Saline Flush Syringe 10mL used in POWERWAND XL kits due to packaging holes risking contamination. Affected units have specific lot numbers. Stop using immediately to prevent infection.
Saline Flush Syringe compromised sterility due to holes in the packaging.
Access Scientific is recalling BD PosiFlush SF Saline Flush Syringes used with POWERWAND XL kits because the packaging has holes that could compromise sterility. This means the syringes might not be sterile, increasing infection risk during medical procedures.
The syringes' packaging has holes that can let contaminants enter the sterile product. This compromises sterility, meaning the syringes might not be safe for medical use, potentially causing infections during procedures.
Healthcare professionals using the syringes for blood draws or IV fluids are most at risk. Patients receiving treatments with these syringes could face infections if the packaging holes allow contamination.
Check for lot numbers: 259731, 261932, 263922, 267010, 268210, 269118, 269714, 270347, 270778. The product is used in POWERWAND XL 4Fr 8cm Max Barrier Kits and has the reference code 94106/10859821006176.
Discard the syringe if you have the affected lot numbers listed above.
The packaging has holes that can compromise sterility, increasing infection risk during medical procedures.
Lot numbers 259731, 261932, 263922, 267010, 268210, 269118, 269714, 270347, 270778.
Check the lot number on the syringe packaging; affected units have the specific lot numbers listed above.
We’ve drafted a message you can send Access Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1976-2020 — Access Scientific Access Scientific Hello, I own a Access Scientific that is covered by recall Z-1976-2020 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.
