OBP Medical Corporation recalls OBP Medical

Recalling company

OBP Medical Corporation

Product

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

Reason

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Jul 13, 2026

Reported

Aug 19, 2026

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 the countries of HKG, CAN, NOR, UAE.

Status

Ongoing

Quantity

8,224 boxes (148,032 units)

Lot / codes

UDI: (01)20888937027451/ Lots: 24J1202Z, 25D2302Z, 25A0202Z, 25E1502Z, 25B2802Z, 25L0802Z

Company location

Lawrence, MA

Recall type

Voluntary: Firm initiated

Recall number

Z-2933-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2933-2026 in the FDA Enforcement Report. Also see FDA recall press releases.