O&M HALYARD INC recalls
Every recall we track for O&M HALYARD INC — 8 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from O&M HALYARD INC fell by more than half in 2025 (1, down from 4 in 2024). 13% rated “stop using now”.
All FDA recall records for O&M HALYARD INC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 1 | 0 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 4 | 0 | 4 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled O&M HALYARD INC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All O&M HALYARD INC recalls
7 shown- Lower riskMedical device
O&M HALYARD INC recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.),
Halyard Purezero Ultraviolet Nitrile Exam Gloves with reference numbers 48771-48775 may fail to meet chemical permeation standards. Consumers should check packaging for UDI codes to determine if affected.
HalyardApr 13, 2026 - Use cautionMedical device
O&M HALYARD INC recalls Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029
O&M HALYARD recalls two orthopedic surgical drape packs with potential open seals that could compromise sterility. Affected packs have specific model numbers and dates. Consumers should check their items and contact the company for details.
O&M HALYARDJul 17, 2025 - Lower riskMedical device
O&M HALYARD, INC. recalls Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product
HALYARD recalls Laparotomy Pack model 88231 due to elevated anti-block/slip additive residues in sterile packaging. This could compromise surgical safety. Affected units include specific lot numbers and expiration dates.
HALYARDNov 26, 2024 - Lower riskMedical device
O&M HALYARD, INC. recalls O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117
O&M Halyard recalls yellow disposable surgical masks with SO SOFT* earloops (Product Code 47117) due to failing EU bioburden testing standards. Masks sold in the U.S. don't require this standard but must comply if labeled.
O&M HALYARDNov 8, 2024 - Lower riskMedical device
O&M HALYARD, INC. recalls HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100)
O&M HALYARD recalls 300-count blue surgical hood (model 69110) mislabeled as surgical cap. Affected units sold in 2022-2023; no safety risk but may cause confusion.
O&M HALYARDFeb 20, 2024 - Stop using nowMedical device
O&M HALYARD, INC. recalls FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with SO SOFT* Lining, Orange, size small, Product
O&M HALYARD recalls Fluidshield 3 N95 masks with soft lining that failed filtration tests, risking inadequate protection from particles.
O&M HALYARDAug 9, 2023 - Lower riskMedical device
O&M HALYARD INC recalls HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
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.
HalyardSep 27, 2021
O&M HALYARD INC recall questions
How many recalls has O&M HALYARD INC had?
8 recalls from O&M HALYARD INC are on record with U.S. safety agencies, from 2021–2026.
What is the most recent O&M HALYARD INC recall?
O&M HALYARD INC recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.),, dated Apr 13, 2026. Every O&M HALYARD INC recall is listed on this page, newest first.
What should I do if I have a recalled O&M HALYARD INC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new O&M HALYARD INC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.