OBP Medical — Class II medical device recall Z-2933-2026
Ongoing recall by OBP Medical Corporation, reported 2026-08-19, distributed nationwide. There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduc
| Recall number | Z-2933-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | OBP Medical Corporation, Lawrence, MA, United States |
| Recall initiated | 2026-07-13 |
| Classified | 2026-08-10 |
| Reported by FDA | 2026-08-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE |
| UPC / GTIN / UDI-DI | 20888937027451 |
| Lot numbers | 24J1202Z, 25A0202Z, 25B2802Z, 25D2302Z, 25E1502Z, 25L0802Z |
| Model numbers | C020130-1 |
Product
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
Reason for recall
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.
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-2933-2026. 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.