FDA · Class II · August 19, 2026

OBP Medical recall: ER-Spec Single-Use Vaginal Speculum with LED Light Source

OBP Medical Corporation is recalling ER-Spec Single-Use Vaginal Speculum with LED Light Source – 8,224 boxes (148,032 units). The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on July 13, 2026. Distributed nationwide.

Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.

Illustration: An FDA laboratory that tests medical devices – not the recalled product. Photo: U.S. Food and Drug Administration, public domain.

Product	ER-Spec Single-Use Vaginal Speculum with LED Light Source
Brand	OBP Medical
Company	OBP Medical Corporation
Type	Medical devices
Classification	Class II
Recall date	July 13, 2026
Published by FDA	August 19, 2026
Quantity	8,224 boxes (148,032 units)
Recall ID	99433

As listed by FDA

Recalled products

OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
FDA recall number
Z-2933-2026
Codes, lots and dates
UDI: (01)20888937027451/ Lots: 24J1202Z, 25D2302Z, 25A0202Z, 25E1502Z, 25B2802Z, 25L0802Z
Quantity
8,224 boxes (148,032 units)
Classification
Class II

Exactly as the agency lists them

Identifiers and details

FDA event ID: 99433
Initiated: Voluntary: Firm initiated
Status: Ongoing
Firm location: Lawrence, MA, United States

Why it was recalled

The reason the FDA lists: “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.”

Where it was sold

Nationwide. Distribution as the FDA records it: “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.”

What to do

Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.

Official notice: FDA Enforcement Report record (event 99433, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.

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FAQ

About this recall

Is OBP Medical ER-Spec Single-Use Vaginal Speculum with LED Light Source recalled?

Yes. OBP Medical Corporation recalled it on July 13, 2026; FDA published it August 19, 2026 (Class II). Only the lots, dates or models listed on this page are included.

Why was it recalled?

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 should I do if I have it?

Where was it sold?

Nationwide.

Recalls

More recalls

Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.