OBP Medical ER-Spec Vaginal Speculum Recall: Burr Risk
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.
Lower-risk 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.
What happened, in plain English
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. Read more at govinfonow.com/recall/459410-obp-medical-er-spec-vaginal-speculum-recall-burr-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/459410-obp-medical-er-spec-vaginal-speculum-recall-burr-risk · Updated August 27, 2026 · FDA enforcement record: FDA #Z-2933-2026
Cite this page
“OBP Medical ER-Spec Vaginal Speculum Recall: Burr Risk.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/459410-obp-medical-er-spec-vaginal-speculum-recall-burr-risk. Based on FDA recall #Z-2933-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2933-2026%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
OBP Medical- Product
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1- Category
Medical device
What to do — step by step
Check Product Details
Look for the reference code C020130-1 and specific lots listed in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 42 states.
FDA distribution: “Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV and…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 37 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2933-2026 (July 13, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2933-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.