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Lower risk Medical device recall · FDA · Published February 27, 2024

ConvaTec CarboFlex Odor Control Dressing Recall: Sterility Risk

ConvaTec recalls sterile odor control dressings that don't meet sterility standards. Affected units include specific lot numbers and packaging. Consumers should check their product details to determine if recalled.

🇺🇸 FDA recall #Z-1495-2024Medical deviceConvaTec ›
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Recalling firmConvaTec, Inc7815 National Service Rd Ste 600 · Greensboro, NC 27409-9403
✎ GovInfoNow plain-language explainer

ConvaTec is recalling sterile odor control dressings that fail to meet sterility standards. This could lead to infections if used improperly. Affected items have specific lot numbers and packaging details. Read more at govinfonow.com/recall/56054-convatec-carboflex-odor-control-dressing-recall-sterility-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/56054-convatec-carboflex-odor-control-dressing-recall-sterility-risk · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1495-2024

Cite this page

“ConvaTec CarboFlex Odor Control Dressing Recall: Sterility Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/56054-convatec-carboflex-odor-control-dressing-recall-sterility-risk. Based on FDA recall #Z-1495-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1495-2024%22&limit=1).

The FDA announced on Feb. 27, 2024, that ConvaTec, Inc. is recalling ConvaTec CarboFlex odor control dressings because they do not meet sterility assurance levels. The agency classified the Class II recall as voluntary.

How to tell if you have it

  • Brand: ConvaTec
  • Product: ConvaTec CarboFlex, 15cm x 20cm, 6 in. x 8 in., Order No. 403204, Odor Control Dressing, Sterile
  • Lot numbers: 3J00675, 3J02320, 3J02332, 3L04811, and 4A00343

The hazard

According to the FDA, the ConvaTec CarboFlex dressings do not meet sterility assurance levels. The recall involves 63 market units distributed in California, Missouri, New Mexico, Pennsylvania, Texas, and Washington.

Context

GovInfoNow's records show ConvaTec, Inc. has had 17 other recalls since Oct. 26, 2017. Recent brand recalls include ConvaTec Esteem Body Soft Urostomy Pouches on July 6, 2026, and ConvaTec Aquacel Ag Surgical SP Dressings on June 8, 2026. Other recent recalls of similar products include DeRoyal Covaderm Plus Dressing (May 18, 2026) and Medline Convenience Kits (June 12, 2026).

How to tell if you have this one

Check for the product name 'ConvaTec CarboFlex', size 15cm x 20cm (6 in. x 8 in.), and order number 403204. Look for lot numbers 3J00675, 3J02320, 3J02332, 3L04811, or 4A00343.

  • Brand
    ConvaTec
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Identify the lot number and packaging to confirm if your ConvaTec CarboFlex dressing is affected.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 6 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: named in the noticeWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: nationwideWIMichigan: nationwideMINew York: nationwideNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: named in the noticePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: named in the noticeMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: named in the noticeNMKansas: nationwideKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: nationwideNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: nationwideGAHawaii: nationwideHITexas: named in the noticeTXFlorida: nationwideFL

FDA distribution: “US Nationwide distribution in the states of CA, MO, NM, PA, TX, and WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Missouri, New Mexico, Pennsylvania, Texas, Washington.

Recall timeline

FDA published this recall 50 days after the firm started it.

1. Firm started the recall: Feb 27, 202412. FDA classified it Class II: Apr 8, 202423. Published in FDA’s Enforcement Report: Apr 17, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #Z-1495-2024 (February 27, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1495-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA