Ethicon recalls PERMA-HAND Silk Suture Size 5, Black 30" (75cm) Double Armed LR Needles (Product Code 485T) due to incorrect suture size in packaging. This could lead to improper use during medical procedures.
The sutures inside the packaging are not the same size or type as indicated on the label.
Ethicon is recalling PERMA-HAND Silk Suture Size 5, Black 30" (75cm) Double Armed LR Needles (Product Code 485T) because the sutures in the packaging don't match the label. This could cause improper use during medical procedures if the wrong suture size is used.
The sutures inside the packaging are not the same size or type as labeled. This mismatch could lead to using the wrong suture size during medical procedures, potentially causing improper tissue approximation or ligation.
Medical professionals who use these sutures for procedures like cardiovascular, ophthalmic, or neurological surgeries may be affected. Patients undergoing such procedures could be at risk if the incorrect suture is used.
Check for the product code 485T on the packaging. The suture is black, 30 inches (75cm) long, and labeled as PERMA-HAND Silk Suture Size 5, Double Armed LR Needles. Product lot MEH906 is also associated with this recall.
Verify the product code 485T and lot number MEH906 on the packaging to confirm if it's recalled.
The recall indicates the sutures in the packaging do not match the label, so they may not be safe for use as intended. Medical professionals should not use these specific units without confirming the correct suture size.
Check the packaging for product code 485T and lot number MEH906. If you have these items, contact Ethicon for guidance on next steps.
The recall states the sutures inside the packaging are not the same size or type as labeled, so using them could lead to improper use during medical procedures.
We’ve drafted a message you can send Ethicon to request your refund or repair — edit it as you like.
Subject: Recall Z-0747-2019 — Ethicon Ethicon Hello, I own a Ethicon that is covered by recall Z-0747-2019 from Ethicon. 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.
