Access Scientific recalls POWERWAND XL 4Fr 10cm Maximum Barrier Kit due to mislabeled catheter length, which could cause treatment delays or user dissatisfaction. No immediate action needed.
Convenience kit mislabeled with the incorrect catheter effective length on the device label and the packaging label. Use may lead to a delay or interruption of treatment and user dissatisfaction or annoyance.
Access Scientific is recalling their POWERWAND XL 4Fr 8cm Maximum Barrier Kit because the device label and packaging incorrectly state the catheter's effective length. This mislabeling might cause treatment delays or patient dissatisfaction but does not pose a safety risk.
The kit's label and packaging incorrectly state the catheter's effective length. This could lead to treatment delays or patient dissatisfaction if healthcare providers or patients misunderstand the device's specifications.
Healthcare professionals using the POWERWAND XL kit for intravenous access or contrast injections may be affected. Patients receiving treatments with this kit could experience delays or frustration due to the mislabeling.
Check for the POWERWAND XL 4Fr 8cm Maximum Barrier Kit with Catalog No. 94108. Look for lot numbers 269939, 270552, 270874, or 272261 on the device or packaging.
Verify the device label and packaging for the correct catheter length as specified in the recall notice.
No, the recall is for mislabeling that could cause treatment delays or patient dissatisfaction, not a safety hazard.
Check the kit's label and packaging for the correct catheter length; no action is needed if the labeling is accurate.
Lot numbers 269939, 270552, 270874, and 272261 are affected.
We’ve drafted a message you can send Access Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-2550-2020 — Access Scientific Access Scientific Hello, I own a Access Scientific that is covered by recall Z-2550-2020 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.
