Recall archive / FDA device enforcement
Colonoscope, Model Number CF-HQ190L. — FDA record Z-1207-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jan 11, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Colonoscope, Model Number CF-HQ190L.
- Reason
- Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.
- Classification
- Class II
- Recalling firm
- Olympus Corporation of the Americas
- Quantity
- 97
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1207-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model Number: CF-HQ190L; UDI DI: 04953170305115; Serial Number: 2082724, 2082896, 2082936, 2083461, 2083765, 2084560, 2085050, 2186261, 2187110, 2187274, 2187811, 2188037, 2188206, 2200530, 2201625, 2201677, 2201844, 2202345, 2288483, 2288940, 2289129, 2289391, 2289421, 2289572, 2290978, 2291472, 2303312, 2304024, 2304070, 2314598, 2315390, 2391750, 2391772, 2391857, 2392281, 2417328, 2417450, 2417702, 2417736, 2417755, 2418202, 2418754, 2418843, 2419006, 2419007, 2419105, 2510489, 2510795, 2510801, 2511164, 2512292, 2512458, 2512470, 2512569, 2512817, 2513285, 2524619, 2524916, 2625144, 2635605, 2635832, 2636020, 2636500, 2636782, 2637892, 2659060, 2659357, 2759754, 2761671, 2762243, 2772492, 2773247, 2773259, 2773324, 2773552, 2874236, 2875490, 2875615, 2875616, 2875656, 2876636, 2876811, 2876877, 2877237, 2877319, 2877901, 2978291, 2978331, 2978640, 2979287, 2979510, 2980281, 2980304, 2980541, 2981322, 2982038, 2982143; |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Nationwide distribution.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Mar 6, 2024
- Recall initiation date
- Jan 11, 2024
- Center classification date
- Feb 29, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.