[Recalled] AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs. — Cutter was longer than was stated on the label | FDA 2011-03-31
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs. |
|---|---|
| Brand / manufacturer | The Anspach Effort, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0829-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 31 March 2011 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Cutter was longer than was stated on the label
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 The Anspach Effort, 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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