Access Scientific recalls BD PosiFlush SF Saline Flush Syringe 10mL used in POWERWAND XL kits due to packaging holes compromising sterility. Affected units have REF/UDI 94116/10859821006237. No remedy specified in official notice.
Saline Flush Syringe compromised sterility due to holes in the packaging.
Access Scientific recalls BD PosiFlush SF Saline Flush Syringes used with POWERWAND XL kits because packaging holes risk contamination. This could lead to infections if used for blood draws or IV fluids. The recall affects specific units with the REF/UDI code 94116/10859821006237.
The syringe packaging has holes that could allow contaminants to enter the sterile product. This poses a risk of infection if the syringe is used for blood sampling or intravenous fluid administration.
Healthcare professionals using the syringe for blood draws or IV fluids are most at risk. The recall affects specific units with the REF/UDI code 94116/10859821006237.
Check for the REF/UDI code 94116/10859821006237 on the packaging. The product is used in POWERWAND XL 5Fr 8cm Max Barrier Kits for blood draws and IV fluids.
Look for the REF/UDI code 94116/10859821006237 on the syringe packaging to confirm if it's affected.
The syringe packaging has holes that could allow contaminants to enter, risking infection during blood draws or IV fluid administration.
The official recall notice does not specify any remedy for this issue.
Check for the REF/UDI code 94116/10859821006237 on the syringe packaging. The product is used in POWERWAND XL 5Fr 8cm Max Barrier Kits.
We’ve drafted a message you can send Access Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1983-2020 — Access Scientific Access Scientific Hello, I own a Access Scientific that is covered by recall Z-1983-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
