Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported June 14, 2017
Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017
Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the clos…
Zimmer Biomet Spine Inc. recalled Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting … - a moderate-severity action.
Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting … was recalled by Zimmer Biomet Spine Inc. in June 14, 2017. Reason: Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiti…. Check the official notice for the remedy. Verify recall #Z-2318-2017 with the FDA Devices before acting.
The recall
Zimmer Biomet Spine Inc. issued this moderate-severity FDA Devices recall-Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiti….
- Moderate
- severity level
- 497 units
- affected scope
- Class II
- classification
- June 14, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2318-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2318-2017) was formally reported on June 14, 2017, with the manufacturer initiating the action on May 10, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Zimmer Biomet Spine Inc. is listed as the recalling firm, operating out of Westminster, CO. Federal records list the affected scope as 497 units.
The documented reason for this recall is: Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closure top the driver has the potential to … Distribution data in the federal record shows the product reached: Nationwide, military/VA/govt and foreign consignee (No Canadian consignees). 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
497 units
Related Recalls
6
3 from same agency
Product description
Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017
Reason for recall
Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closure top the driver has the potential to create a torsional spring which can cause damage and the potential for the values of torque to go out of specification.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2318-2017 |
| Date reported | June 14, 2017 |
| Date initiated | May 10, 2017 |
| Recalling firm | Zimmer Biomet Spine Inc. |
| Firm location | Westminster, CO |
| Affected scope | 497 units |
| Distribution | Nationwide, military/VA/govt and foreign consignee (No Canadian consignees) |
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-2318-2017) 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? ▼
Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017. Recalled by Zimmer Biomet Spine Inc.. Units affected: 497 units.
Why was this product recalled? ▼
Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closure top the driver has the potential to create a torsional spring which can cause damage and the potential for the values of torque to go out of specification.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 14, 2017. Severity: Moderate. Recall number: Z-2318-2017.
Where was the recalled product distributed? ▼
Distribution: Nationwide, military/VA/govt and foreign consignee (No Canadian consignees).
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2318-2017) 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 June 14, 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.