MICROFLEX Diamond Grip Examination Gloves — Class II medical device recall Z-0051-2021
Terminated recall by Ansell Healthcare Products LLC, reported 2020-10-14, distributed nationwide. Examination gloves were shipped inadvertently, without to verify barrier integrity.
| Recall number | Z-0051-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ansell Healthcare Products LLC, Reno, NV, United States |
| Recall initiated | 2020-08-19 |
| Classified | 2020-10-02 |
| Reported by FDA | 2020-10-14 |
| Terminated | 2021-11-03 |
| Distributed | Nationwide (US) |
| Quantity | 1,312 cases |
| Lot numbers | 20035314LG, 2003LG |
Product
MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner s hand or finger to prevent contamination between patient and examiner.
Reason for recall
Examination gloves were shipped inadvertently, without to verify barrier integrity.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0051-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.