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Use caution Medical device recall · FDA · Published September 11, 2017

Zimmer Biomet Cut Resistant Surgical Glove Liners Recall: Lack Sterility Assurance

Zimmer Biomet recalls cut-resistant surgical glove liners that lack sterility assurance. Affected items have specific item and lot numbers. Consumers should stop using these liners to prevent infection risks during medical procedures.

🇺🇸 FDA recall #Z-0609-2018Medical deviceZimmer Biomet ›
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Recalling firmZimmer Biomet, Inc.56 E Bell Dr · Warsaw, IN 46582-6989
✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling cut-resistant surgical glove liners that lack sterility assurance. This means the liners could cause infections during medical procedures if used without proper sterilization. Read more at govinfonow.com/recall/73039-zimmer-biomet-cut-resistant-surgical-glove-liners-recall-lack-sterility.

Source Summary by GovInfoNow · govinfonow.com/recall/73039-zimmer-biomet-cut-resistant-surgical-glove-liners-recall-lack-sterility · Updated September 18, 2026 · FDA enforcement record: FDA #Z-0609-2018

Cite this page

“Zimmer Biomet Cut Resistant Surgical Glove Liners Recall: Lack Sterility Assurance.” GovInfoNow, updated September 18, 2026. https://govinfonow.com/recall/73039-zimmer-biomet-cut-resistant-surgical-glove-liners-recall-lack-sterility. Based on FDA recall #Z-0609-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0609-2018%22&limit=1).

Why it’s dangerous

The liners are made from stainless steel and synthetic fibers woven together to form a cut-resistant material. However, they lack sterility assurance, meaning they may not be properly sterilized and could introduce infections during medical procedures.

Who’s affected

Surgical professionals and medical facilities using Zimmer Biomet's BlockAid Cut Resistant Surgical Glove Liners are affected. Those handling the liners without proper sterilization are at risk of infection.

How to tell if you have this one

Check for item numbers 650126 through 650131 and corresponding lot numbers listed in the recall notice. These liners are sold with expiration dates up to April 2022.

  • Brand
    Zimmer Biomet
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Liners

    Immediately stop using the recalled BlockAid Cut Resistant Surgical Glove Liners to prevent infection risks during medical procedures.

Where it went and when

Where it was distributed

Distributed in 28 states and D.C., and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: yesIDMontana: yesMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “Distributed in 29 states: AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MO, MT, NC, NE, NJ, NY, OH, OR, PA, SC, TN, TX, VA, WV and Washington, DC. Distributed to 1 Veteran's Administration hospital in MO. Distributed in…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Colorado, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Missouri, Montana, Nebraska, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, West Virginia.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Sep 11, 201712. FDA classified it Class II: Feb 14, 201823. Published in FDA’s Enforcement Report: Feb 21, 201834. FDA terminated the recall: Aug 30, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

Do I need to replace these liners?

Yes, you should stop using the recalled liners and replace them with sterile surgical gloves.

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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-0609-2018 (September 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0609-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on September 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