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Lower risk Medical device recall · FDA · Published March 20, 2024

3M Durapore Surgical Tape: Incorrect 5-Year Shelf Life Label

3M recalls Durapore Surgical Tape (Catalog 1538-118) with incorrect 5-year shelf life label instead of 3 years. Affected lots may expire sooner than intended.

🇺🇸 FDA recall #Z-1633-2024Medical device3M ›
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Recalling firm3M Company - Health Care Business3m Center 2510 Conway Ave, Bldg 275-5w-06 · Saint Paul, MN 55144-0001
✎ GovInfoNow plain-language explainer

What happened, in plain English

3M is recalling specific lots of Durapore Surgical Tape (Catalog 1538-118) because some were labeled with a 5-year shelf life instead of the correct 3-year shelf life. This means the tape could expire earlier than intended, potentially causing issues with product safety or effectiveness. Read more at govinfonow.com/recall/55815-3m-durapore-surgical-tape-incorrect-5-year-shelf-life-label.

Source Summary by GovInfoNow · govinfonow.com/recall/55815-3m-durapore-surgical-tape-incorrect-5-year-shelf-life-label · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1633-2024

Cite this page

“3M Durapore Surgical Tape: Incorrect 5-Year Shelf Life Label.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55815-3m-durapore-surgical-tape-incorrect-5-year-shelf-life-label. Based on FDA recall #Z-1633-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1633-2024%22&limit=1).

Why it’s dangerous

The tape was incorrectly labeled with a 5-year shelf life instead of the standard 3-year shelf life. This could lead to the tape becoming ineffective or unsafe before the intended expiration date, potentially affecting medical procedures.

Who’s affected

Healthcare professionals and individuals using surgical tape for medical purposes who own the affected lots. Those most at risk are users who rely on the tape for critical medical applications.

How to tell if you have this one

Check for the catalog number 1538-118 and lot codes listed: 33DER3, 33DTMA, 33DTPN, 33EDDE, 33ETFA, 33ETHX, 33FDHA, 33FDYN, 33FE9D, 33FEY6, 33FTLA, 33FW6E, 33FWPC, 33JE7T, 33JEFK, 33JENC, 33JYPX, 33JYW5, 33K3EJ, 33KPWT, 33KT6R, 33KT8F, 33LJWC, 33LK5M, 33LLEY, 33LLPT, 33LM6R, 33LMET, 33LMX3, 33N56W, 33N5K4, 33N5TC, 33NF36, 33NF6A, 33NY98, 33NYP9, 33P37P, 33PKLN, 33PL6J, 33PMFA, 33R35M, 33R3P6, 33RMNF, 33RNP4, 33TL39, 33TL8F, 33TLF4, 33TN55, 33WEA8, 33WEHJ, 33WERX, 33WF5P, 33WFD5.

  • Brand
    3M
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the catalog number 1538-118 and lot codes listed in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 11 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: named in the noticeNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: named in the noticeILWisconsin: nationwideWIMichigan: nationwideMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: nationwideINOhio: nationwideOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: nationwideMOKentucky: nationwideKYWest Virginia: nationwideWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: nationwideDEArizona: named in the noticeAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: named in the noticeNCSouth Carolina: nationwideSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “Worldwide distribution - US Nationwide in the states of TX, NY, NH, AZ, NC, CA, IL, GA, VA, MD, FL, and the country of Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arizona, California, Florida, Georgia, Illinois, Maryland, New Hampshire, New York, North Carolina, Texas, Virginia.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: Mar 20, 202412. FDA classified it Class II: Apr 24, 202423. Published in FDA’s Enforcement Report: May 1, 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-1633-2024 (March 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1633-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 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