Medela recalls Invia Foam Dressing Kit with FitPad X-Large (3 pcs) SKU #0876224 due to potential holes in sterile packaging. This could compromise sterility during medical use. Affected units were sold with specific expiration dates.
Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging.
Medela is recalling Invia Foam Dressing Kit with FitPad X-Large (3 pcs) SKU #0876224 because the sterile packaging might have holes. This could allow contamination during medical procedures, making the dressing unsafe for use.
The sterile packaging could develop holes, potentially allowing contaminants to enter the dressing. This might compromise the sterility needed for medical procedures, increasing infection risk.
Healthcare professionals and patients using this dressing kit for medical care. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the product name 'Invia Foam Dressing Kit with FitPad - X-Large (3 pcs)' and SKU #0876224. Look for lot numbers: 17110012731 (exp 17-Nov-19), 17110022736 (exp 22-Nov-19), 17120012746 (exp 8-Dec-19), 18010012767 (4-Jan-20), 18070012913 (31-Jul-20), 18090012960 (exp 28-Sep-20), 18110013046 (5-Nov-20).
Verify the product name, SKU, and lot numbers to confirm if your kit is affected.
The sterile packaging could have holes, potentially allowing contaminants to enter the dressing during medical use.
The recall record does not specify a remedy, so check the product details to confirm if it's affected.
Yes, affected lots include 17110012731 (exp 17-Nov-19), 17110022736 (exp 22-Nov-19), 17120012746 (exp 8-Dec-19), 18010012767 (4-Jan-20), 18070012913 (31-Jul-20), 18090012960 (exp 28-Sep-20), and 18110013046 (5-Nov-20).
We’ve drafted a message you can send Medela to request your refund or repair — edit it as you like.
Subject: Recall Z-0773-2020 — Medela Medela Hello, I own a Medela that is covered by recall Z-0773-2020 from Medela. 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.
