[Recalled] CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 22mm Material Number: 66-122 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as n
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 22mm Material Number: 66-122 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of the disc confirmed b |
|---|---|
| Brand / manufacturer | RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1243-2021 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 15 January 2021 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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