Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported August 27, 2025
Pentax Medical Video Processor; Model Number: EPK-i8020c;
During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have obser…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Pentax of America Inc recalled Pentax Medical Video Processor; Model Number: EPK-i8020c; - a moderate-severity action.
Pentax Medical Video Processor; Model Number: EPK-i8020c; was recalled by Pentax of America Inc in August 27, 2025. Reason: During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endo…. Check the official notice for the remedy. Verify recall #Z-2329-2025 with the FDA Devices before acting.
The recall
Pentax of America Inc issued this moderate-severity FDA Devices recall-During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endo….
- Moderate
- severity level
- 144 units
- affected scope
- Class II
- classification
- August 27, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2329-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2329-2025) was formally reported on August 27, 2025, with the manufacturer initiating the action on July 16, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Pentax of America Inc is listed as the recalling firm, operating out of Montvale, NJ. Federal records list the affected scope as 144 units.
The documented reason for this recall is: During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke like steam and noted that the … Distribution data in the federal record shows the product reached: US Distribution to states of: AZ, CA, DC, FL IA, ID, IL, KS, MA, MD, MI, MO, NC, NJ, NM, NY, OK, PA, TX, WA.. 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
144 units
Related Recalls
6
3 from same agency
Product description
Pentax Medical Video Processor; Model Number: EPK-i8020c;
Reason for recall
During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient and may cause thermal injury to the patient s mucous membrane.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2329-2025 |
| Date reported | August 27, 2025 |
| Date initiated | July 16, 2025 |
| Recalling firm | Pentax of America Inc |
| Firm location | Montvale, NJ |
| Affected scope | 144 units |
| Distribution | US Distribution to states of: AZ, CA, DC, FL IA, ID, IL, KS, MA, MD, MI, MO, NC, NJ, NM, NY, OK, PA, TX, WA. |
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-2329-2025) 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? ▼
Pentax Medical Video Processor; Model Number: EPK-i8020c;. Recalled by Pentax of America Inc. Units affected: 144 units.
Why was this product recalled? ▼
During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient and may cause thermal injury to the patient s mucous membrane.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 27, 2025. Severity: Moderate. Recall number: Z-2329-2025.
Where was the recalled product distributed? ▼
Distribution: US Distribution to states of: AZ, CA, DC, FL IA, ID, IL, KS, MA, MD, MI, MO, NC, NJ, NM, NY, OK, PA, TX, WA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2329-2025) 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 August 27, 2025. 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.