OBP Medical recalls X-Small ER-Spec vaginal speculums with LED light due to potential burr on plastic blade that could cause sharp edges for patient or provider.
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.
OBP Medical is recalling X-Small ER-Spec vaginal speculums with LED light for possible burrs on the plastic blade that could cause sharp edges during use. This could lead to injury for both patients and healthcare providers.
The speculum may have a burr on the plastic blade that creates a sharp edge. This sharp edge could cause injury to the patient or healthcare provider during use.
Healthcare providers and patients using the X-Small ER-Spec vaginal speculums with LED light source. Those most at risk are individuals who have used the speculum recently.
Check for the X-Small size with LED light source. The product has a reference code (REF) C020130-1 and was sold in lots 24J1202Z, 25D2302Z, 25A0202Z, 25E1502Z, 25B2802Z, 25L0802Z.
Look for the reference code C020130-1 and specific lots listed in the recall notice.
The recall states there is a potential for a burr on the plastic blade that could cause sharp edges, but the risk is low and not all products are affected.
Check for the X-Small size with LED light source and reference code C020130-1 in lots 24J1202Z, 25D2302Z, 25A0202Z, 25E1502Z, 25B2802Z, or 25L0802Z.
The recall does not specify a remedy, so check with OBP Medical for further instructions.
We’ve drafted a message you can send OBP Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2933-2026 — OBP Medical OBP Medical Hello, I own a OBP Medical that is covered by recall Z-2933-2026 from OBP Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
