Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported February 7, 2024
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilize…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Vortex Surgical Inc. recalled Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25 - a moderate-severity action.
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25 was recalled by Vortex Surgical Inc. in February 7, 2024. Reason: Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The…. Check the official notice for the remedy. Verify recall #Z-0970-2024 with the FDA Devices before acting.
The recall
Vortex Surgical Inc. issued this moderate-severity FDA Devices recall-Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The….
- Moderate
- severity level
- 800 units
- affected scope
- Class II
- classification
- February 7, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0970-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0970-2024) was formally reported on February 7, 2024, with the manufacturer initiating the action on December 18, 2023. It is classified under Moderate severity (Class II), with a current status of Terminated. Vortex Surgical Inc. is listed as the recalling firm, operating out of Saint Charles, MO. Federal records list the affected scope as 800 devices.
The documented reason for this recall is: Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps … Distribution data in the federal record shows the product reached: Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and the country of Republic of Korea. 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
800 devices
Related Recalls
6
3 from same agency
Product description
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Reason for recall
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0970-2024 |
| Date reported | February 7, 2024 |
| Date initiated | December 18, 2023 |
| Recalling firm | Vortex Surgical Inc. |
| Firm location | Saint Charles, MO |
| Affected scope | 800 devices |
| Distribution | Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and the country of Republic of Korea |
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-0970-2024) 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? ▼
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25. Recalled by Vortex Surgical Inc.. Units affected: 800 devices.
Why was this product recalled? ▼
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 7, 2024. Severity: Moderate. Recall number: Z-0970-2024.
Where was the recalled product distributed? ▼
Distribution: Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and the country of Republic of Korea.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0970-2024) 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 February 7, 2024. 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.