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FDA
Food and Drug Administration · Recall Z-2933-2026 · Jul 13, 2026

OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

OBP Medical Corporation

The hazard

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. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDI: (01)20888937027451/ Lots: 24J1202ZModel 25D2302ZModel 25A0202ZModel 25E1502ZModel 25B2802ZModel 25L0802ZUPC 20888937027451

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.