Access Scientific recalls BD PosiFlush SF Saline Flush Syringes with packaging holes that could compromise sterility. Affected units include specific lot numbers from 259489 to 268776. 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 that may have holes in the packaging, risking contamination. This could lead to infections if used for medical procedures. Affected units have specific lot numbers listed in the recall.
The syringe packaging may have holes that allow contaminants to enter the sterile product. This could lead to infections if the syringe is used for blood sampling or administering fluids intravenously.
Healthcare professionals and patients using the BD PosiFlush SF Saline Flush Syringe for intravenous procedures are most at risk. The recall affects specific lot numbers produced between 2019 and 2023.
Check the lot numbers on the syringe packaging: 259489, 259956, 261313, 262479, 263893, 265955, 266809, 267719, or 268776. The syringe is part of the POWERWAND XL Alternate Site Kit, 4Fr, with reference number 80701/10859821006213.
Inspect the syringe packaging for holes that could compromise sterility.
The syringe packaging may have holes that allow contaminants to enter, risking infection during medical procedures.
Affected lot numbers are 259489, 259956, 261313, 262479, 263893, 265955, 266809, 267719, and 268776.
The syringe is part of the POWERWAND XL Alternate Site Kit, 4Fr, with reference number 80701/10859821006213 and the listed lot numbers.
We’ve drafted a message you can send Access Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1973-2020 — Access Scientific Access Scientific Hello, I own a Access Scientific that is covered by recall Z-1973-2020 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.
