Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported September 20, 2017
Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other purposes.
Fujifilm is reporting a corrective action due to an FDA inspection.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Fujifilm Medical Systems U.S.A., Inc. recalled Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endosc… - a moderate-severity action.
Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endosc… was recalled by Fujifilm Medical Systems U.S.A., Inc. in September 20, 2017. Reason: Fujifilm is reporting a corrective action due to an FDA inspection.. Check the official notice for the remedy. Verify recall #Z-3128-2017 with the FDA Devices before acting.
The recall
Fujifilm Medical Systems U.S.A., Inc. issued this moderate-severity FDA Devices recall-Fujifilm is reporting a corrective action due to an FDA inspection..
- Moderate
- severity level
- Class II
- classification
- September 20, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-3128-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-3128-2017) was formally reported on September 20, 2017, with the manufacturer initiating the action on March 9, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Fujifilm Medical Systems U.S.A., Inc. is listed as the recalling firm, operating out of Wayne, NJ. Federal records list the affected scope as 260 manuals in total.
The documented reason for this recall is: Fujifilm is reporting a corrective action due to an FDA inspection. Distribution data in the federal record shows the product reached: US Nationwide Distribution. 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 - 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 - 40,422 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
260 manuals in total
Related Recalls
6
0 from same agency
Product description
Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other purposes.
Reason for recall
Fujifilm is reporting a corrective action due to an FDA inspection.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-3128-2017 |
| Date reported | September 20, 2017 |
| Date initiated | March 9, 2015 |
| Recalling firm | Fujifilm Medical Systems U.S.A., Inc. |
| Firm location | Wayne, NJ |
| Affected scope | 260 manuals in total |
| Distribution | US Nationwide Distribution |
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-3128-2017) 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? ▼
Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other purposes.. Recalled by Fujifilm Medical Systems U.S.A., Inc.. Units affected: 260 manuals in total.
Why was this product recalled? ▼
Fujifilm is reporting a corrective action due to an FDA inspection.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 20, 2017. Severity: Moderate. Recall number: Z-3128-2017.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-3128-2017) 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 September 20, 2017. 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.