ConvaTec recalls sterile disposable forceps due to potential sterile barrier breach in packaging. Affected units sold with specific lot codes; contact for return instructions.
An internal assessment of packaging confirmed the potential for a breach in the sterile barrier.
ConvaTec is recalling sterile disposable forceps that may have packaging issues risking contamination. This could lead to infections during medical procedures if the forceps are not properly sterile.
The packaging might not maintain sterility properly, potentially allowing contamination. This could lead to infections during medical procedures if the forceps are not sterile when used.
Healthcare professionals and medical facilities using the recalled forceps for wound care procedures. Patients undergoing surgeries or wound treatments are at risk if the forceps become contaminated.
Check for lot codes: 167069, 168288, 171981, 176327, 179936, 182217, 187735, 225174, 231247, 231248, 307362, 307578, 308189, 318432, 318433, 318434, 489868, 489951, 490747, 493969. The forceps are sold in packs of 100.
Look for lot codes on the packaging: 167069, 168288, 171981, 176327, 179936, 182217, 187735, 225174, 231247, 231248, 307362, 307578, 308189, 318432, 318433, 318434, 489868, 489951, 490747, 493969.
An internal assessment found potential for a breach in the sterile barrier of the packaging.
Check the lot codes on the packaging to see if your forceps are affected. Contact ConvaTec for return instructions.
The forceps may not be sterile if the packaging is compromised, which could lead to infections during medical procedures.
We’ve drafted a message you can send ConvaTec to request your refund or repair — edit it as you like.
Subject: Recall Z-1035-2019 — ConvaTec ConvaTec Hello, I own a ConvaTec that is covered by recall Z-1035-2019 from ConvaTec. 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.
