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Lower risk Medical device recall · FDA · Published September 27, 2021

Halyard Sterling Zero Exam Gloves Recall: Discoloration and Tearing Risk

Halyard Sterling Zero nitrite-free exam gloves (sizes XS-SL) may discolor and lose elasticity over time, causing tearing during use. Affected units include specific lot numbers and sizes listed in the recall.

🇺🇸 FDA recall #Z-0317-2022Medical deviceHalyard ›
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Recalling firmO&M HALYARD INC1 Edison Dr · Alpharetta, GA 30004-3894
✎ GovInfoNow plain-language explainer

Halyard Sterling Zero nitrite-free exam gloves (sizes XS, S, M, L, XL) may discolor and lose elasticity over time, making them tear easily when worn. This could lead to injury if gloves fail during use. Read more at govinfonow.com/recall/61750-halyard-sterling-zero-exam-gloves-recall-discoloration-and-tearing-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/61750-halyard-sterling-zero-exam-gloves-recall-discoloration-and-tearing-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0317-2022

Cite this page

“Halyard Sterling Zero Exam Gloves Recall: Discoloration and Tearing Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61750-halyard-sterling-zero-exam-gloves-recall-discoloration-and-tearing-risk. Based on FDA recall #Z-0317-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0317-2022%22&limit=1).

The FDA announced on September 27, 2021, that O&M HALYARD INC is recalling all lots of HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES in sizes XS through XL. The agency cited the hazard that aging gloves may discolor and lose elasticity, preventing users from donning them without tearing.

How to tell if you have it

  • HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
  • UPC 20680651474593 (XS)
  • UPC 20680651474609 (S)
  • UPC 20680651474616 (M)
  • UPC 20680651474623 (L)
  • UPC 20680651474630 (XL)

The hazard

According to the FDA, all lots of the gloves may discolor and lose elasticity upon aging. This condition results in the inability of the user to don the gloves without tearing.

Context

GovInfoNow's records show O&M HALYARD INC has had six other recalls on record since August 9, 2023. Other recent recalls include the Halyard Purezero Ultraviolet Nitrile Exam Gloves Recall (April 13, 2026) and the O&M HALYARD Orthopedic Pack Recall (July 17, 2025). Similar recent recalls of comparable products include the Performance Pro Blue Nitrile Gloves Recall (August 14, 2026) and the AVID Medical Halyard IV Start Kit Non-Sterile Recall (July 14, 2026).

How to tell if you have this one

Check for the following sizes: XS, S, M, L, and XL. Look for the specific lot numbers listed in the recall: REF 47459-47463 with UDI codes starting with (01)20680651474593.

  • Brand
    Halyard
  • Product
    HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Your Gloves

    Identify if your gloves match the recalled sizes and lot numbers listed in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution - US Nationwide and the countries of EU/Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Sep 27, 202112. FDA classified it Class II: Dec 1, 202123. Published in FDA’s Enforcement Report: Dec 8, 202132021
  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-0317-2022 (September 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0317-2022 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