Puritan Medical recalls HydroFlock Sterile Flocked Collection Device (part 25-3317-H) due to mislabeled product distribution. Affected units sold with incorrect part code.
It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in all packages.
Puritan Medical is recalling HydroFlock Sterile Flocked Collection Devices that were mislabeled. This means some units sold as part 25-3317-H actually contain part 25-3317-U, which could lead to incorrect use in medical procedures.
The recall involves mislabeled product where units sold as part 25-3317-H contain part 25-3317-U. This could lead to incorrect use in medical procedures if the wrong device is used.
Healthcare professionals using the HydroFlock device for medical procedures may be affected. Patients receiving care with mislabeled devices could face incorrect treatment.
Check for part number 25-3317-H on the device. Look for lot number S1014 on the packaging. The product was distributed by Puritan Medical Products Company, LLC.
Verify the part number on the device and packaging. If it shows 25-3317-H with lot S1014, it is affected.
The recall is due to mislabeling, not a safety hazard. The device itself is safe but may be used incorrectly if the wrong part is installed.
Check for part number 25-3317-H and lot number S1014 on the device packaging.
The recall does not require immediate action. Check the device label and contact Puritan Medical if you have concerns.
We’ve drafted a message you can send Puritan Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1391-2024 — Puritan Medical Puritan Medical Hello, I own a Puritan Medical that is covered by recall Z-1391-2024 from Puritan Medical. 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.
