Ment: CPX 4 US Breast Tissue Expanders with Suture Tabs (Reference SCPX-157LH, 650cc) may have dull needle tips that are hard to advance or break. Affected patients should contact Mentor Texas for details.
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Mentor Texas is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs (Reference SCPX-157LH, 650cc) because their infusion sets might have dull or blunt needle tips that are difficult to advance or break. This could cause issues during medical procedures.
The infusion sets for these tissue expanders may have dull or blunt needle tips that are difficult to advance or break. This could lead to complications during medical procedures if the needle doesn't move properly or breaks unexpectedly.
Patients with CPX 4 US Breast Tissue Expanders (Reference SCPX-157LH, 650cc) who use the infusion sets for medical procedures are most at risk. The recall applies to those who have the specific reference numbers listed.
Check for the reference number SCPX-157LH on the product label. The expanders are 650cc smooth low height tissue expanders with suture tabs. They were sold with the serial number 10081317028335.
Look for the reference number SCPX-157LH on the product label to confirm if you have the recalled item.
The recall does not require stopping use immediately; patients should contact Mentor Texas for specific guidance.
The official notice does not specify a remedy, so contact Mentor Texas directly for instructions.
The hazard description mentions potential issues with needle advancement or breaking, but no serious injury risk is stated.
We’ve drafted a message you can send Mentor Texas to request your refund or repair — edit it as you like.
Subject: Recall Z-1682-2026 — Mentor Texas Mentor Texas Hello, I own a Mentor Texas that is covered by recall Z-1682-2026 from Mentor Texas. 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.
