Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported December 6, 2023
CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Aizu Olympus Co., Ltd. recalled CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE - a moderate-severity action.
CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE was recalled by Aizu Olympus Co., Ltd. in December 6, 2023. Reason: Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the …. Check the official notice for the remedy. Verify recall #Z-0415-2024 with the FDA Devices before acting.
The recall
Aizu Olympus Co., Ltd. issued this moderate-severity FDA Devices recall-Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the ….
- Moderate
- severity level
- Class II
- classification
- December 6, 2023
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0415-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0415-2024) was formally reported on December 6, 2023, with the manufacturer initiating the action on October 16, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Aizu Olympus Co., Ltd. is listed as the recalling firm, operating out of Aizuwakamatsu. Federal records list the affected scope as 24 incorrectly repaired units.
The documented reason for this recall is: Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or im… Distribution data in the federal record shows the product reached: Domestic distribution to FL, KY, MA, NJ, NY, and PA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
24 incorrectly repaired units
Related Recalls
6
3 from same agency
Product description
CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE
Reason for recall
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0415-2024 |
| Date reported | December 6, 2023 |
| Date initiated | October 16, 2023 |
| Recalling firm | Aizu Olympus Co., Ltd. |
| Firm location | Aizuwakamatsu |
| Affected scope | 24 incorrectly repaired units |
| Distribution | Domestic distribution to FL, KY, MA, NJ, NY, and PA |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0415-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE. Recalled by Aizu Olympus Co., Ltd.. Units affected: 24 incorrectly repaired units.
Why was this product recalled? ▼
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 6, 2023. Severity: Moderate. Recall number: Z-0415-2024.
Where was the recalled product distributed? ▼
Distribution: Domestic distribution to FL, KY, MA, NJ, NY, and PA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0415-2024) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 6, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.