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Urgent Enforcement Amended Final

O&M Halyard Recalls Halyard Purezero Ultraviolet Examination Gloves, R2610893

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Summary

ANSM has relayed a lot withdrawal (recall) of Halyard Purezero Ultraviolet examination gloves initiated by O&M Halyard, Inc. (reference R2610893). The affected products carry dual status as both a medical device and personal protective equipment (PPE/EPI), with the safety concern specifically related to the PPE application. Users have already received direct notification from O&M Halyard, Inc. ANSM is not the originator of this corrective action — it serves solely as a relay of the manufacturer's field safety corrective action notice.

“L'ANSM assure uniquement le relai de cette notification de sécurité.”

ANSM , verbatim from source
Published by ANSM on ansm.sante.fr . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

About this source

ANSM is France's national medicines and medical devices safety agency. Its safety information page publishes drug recalls, medical device field safety notices, batch withdrawals, and benefit-risk reassessments for products on the French market. Around 100 alerts a month, written in French. Many of the affected products are also sold across the EU and UK, so an ANSM recall often previews a wider regulatory response from the EMA, MHRA, BfArM, or AIFA in the days that follow. Watch this if you manufacture or distribute medical devices in Europe, run a hospital pharmacy network, or track post-market safety signals across the European market. Recent recalls include Monnal T60 ventilators, Murex HBsAg reagents, and Arrow Teleflex hemodialysis catheters.

What changed

ANSM issued a safety alert (R2610893) relaying a voluntary lot withdrawal (recall) of Halyard Purezero Ultraviolet examination gloves initiated by O&M Halyard, Inc. The products are classified as both a medical device and personal protective equipment (PPI/EPI), with the safety issue specifically concerning the PPE application. ANSM clarifies it is not the originating authority for this corrective action and is merely serving as a relay of the manufacturer's field safety corrective action notification.

Healthcare facilities and pharmacies that use Halyard Purezero Ultraviolet examination gloves should verify whether any lots covered by R2610893 are in stock. Since users have already received direct correspondence from O&M Halyard, affected parties should review that communication and follow any instructions provided by the manufacturer directly. Questions should be directed to O&M Halyard, Inc., the issuing party of the safety action.

Archived snapshot

Apr 23, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Rappel n° R2610893 destiné aux pharmacies d'usage intérieur et aux établissements de santé L'ANSM a été informée de la mise en œuvre d’un retrait de lots effectué par la société O&M Halyard, Inc.

Les produits concernés ont le double statut dispositif médical et équipement de protection individuel (EPI) et la problématique concerne l’application EPI. L’ANSM assure uniquement le relai de cette notification de sécurité.

Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2610893. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société O&M Halyard, Inc. (23/04/2026)

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Last updated

Classification

Agency
ANSM
Filed
April 23rd, 2026
Instrument
Enforcement
Branch
Executive
Source language
fr
Legal weight
Binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Healthcare providers Medical device makers Retailers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Medical device recall Safety alert notification
Geographic scope
France FR

Taxonomy

Primary area
Medical Devices
Operational domain
Clinical Operations
Topics
Pharmaceuticals Product Safety

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