Smith & Nephew recalls RENASYS EDGE 800ML canisters with solidifier for NPWT patients due to black particulate matter from carbon filters potentially damaging the pump.
Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
Smith & Nephew is recalling RENASYS EDGE 800ML canisters with solidifier for patients using negative pressure wound therapy. Black particles from the carbon filter may damage the pump, which could affect wound healing.
Black particulate matter from the carbon filter in the canister can enter the NPWT pump. This may cause damage to the pump, potentially affecting the wound healing process.
Patients using the RENASYS EDGE 800ML canister with solidifier for negative pressure wound therapy (NPWT) are affected. Those with the specific product numbers or lot numbers listed are most at risk.
Check for the product name 'RENASYS EDGE 800ML CANISTER WITH Solidifier' and product number 66803140 or lot numbers 1016051, 1017549.
Identify if your canister has product number 66803140 or lot numbers 1016051, 1017549.
Black particulate matter from the carbon filter may enter the NPWT pump and cause damage.
The recall record does not specify a remedy, so check product details to see if it's affected.
The recall record does not indicate that the canister is unsafe; it may require checking product details to confirm.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-1597-2024 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-1597-2024 from Smith & Nephew. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.