Severity
Critical
CriticalClass ITerminated
FDA Devices recall · Reported September 26, 2018
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and …
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Pro-Med Instruments Gmbh recalled DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous cranio… - a critical-severity action.
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous cranio… was recalled by Pro-Med Instruments Gmbh in September 26, 2018. Reason: The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and …. Check the official notice for the remedy. Verify recall #Z-2970-2018 with the FDA Devices before acting.
The recall
Pro-Med Instruments Gmbh issued this critical-severity FDA Devices recall-The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and ….
- Critical
- severity level
- 30 units
- affected scope
- Class I
- classification
- September 26, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2970-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2970-2018) was formally reported on September 26, 2018, with the manufacturer initiating the action on July 5, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. Pro-Med Instruments Gmbh is listed as the recalling firm, operating out of Freiburg Im Breisgau, N/A. Federal records list the affected scope as 30 units.
The documented reason for this recall is: The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and failure of the headrest system. Distribution data in the federal record shows the product reached: Worldwide distribution to US states of CA, TX, TN, MS, GA, WV, and OH, Qatar, India, UK, Singapore, Australia, Germany, South Africa, Italy, and Japan. 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
30 units
Related Recalls
6
0 from same agency
Product description
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
Reason for recall
The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and failure of the headrest system.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | Z-2970-2018 |
| Date reported | September 26, 2018 |
| Date initiated | July 5, 2018 |
| Recalling firm | Pro-Med Instruments Gmbh |
| Firm location | Freiburg Im Breisgau, N/A |
| Affected scope | 30 units |
| Distribution | Worldwide distribution to US states of CA, TX, TN, MS, GA, WV, and OH, Qatar, India, UK, Singapore, Australia, Germany, South Africa, Italy, and Japan |
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-2970-2018) 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.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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? ▼
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries. Recalled by Pro-Med Instruments Gmbh. Units affected: 30 units.
Why was this product recalled? ▼
The combination of two different design revisions of DORO LUCENT Base Unit, Locking Transitional Member, and Transitional Member within one set up might lead to a malfunction and failure of the headrest system.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 26, 2018. Severity: Critical. Recall number: Z-2970-2018.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution to US states of CA, TX, TN, MS, GA, WV, and OH, Qatar, India, UK, Singapore, Australia, Germany, South Africa, Italy, and Japan.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2970-2018) 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 26, 2018. 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.