Official recall record

CTP - Tubing sets

What the authority reported

The manufacturer became aware of this issue due to six customer complaint reports. It was found that the sterile barrier was compromised, as the Tyvek lid was found opened prior to use. No harm to any person was reported. An internal investigation has confirmed that all affected products show a consistent similar defect pattern occurring at the same sealing area and were manufactured using the same tool. Therefore, this FSCA is limited to all sterile products within shelf-life manufactured using the same tool. Consignees will be asked to confirm receipt of the field action notification. Consignees will be asked to return all unused, affected sold product from consignee locations.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

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