FDA Device recall Z-0632-2014
Anspach B-Blue-S 11.25 cm attachment and Anspach B-Green Standard Craniotome
- FDA Device
- Class II
- terminated
- Published 2014-01-15
On 2014-01-15 the FDA classified a Class II recall of Anspach B-Blue-S 11.25 cm attachment and Anspach B-Green Standard Craniotome by The Anspach Effort, citing anspach was contacted by a hospital to inform Anspach that a Blackmax motor had been used in a case where the patient was diagnosed with Creutzfeldt-Jacob Disease (CJD).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0632-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-11 |
| Published | 2014-01-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | The Anspach Effort |
| Distribution | MD |
Product
Anspach B-Blue-S 11.25 cm attachment and Anspach B-Green Standard Craniotome. Cutting and shaping bone.
Reason
Anspach was contacted by a hospital to inform Anspach that a Blackmax motor had been used in a case where the patient was diagnosed with Creutzfeldt-Jacob Disease (CJD).
Identifiers
| code_info | Serial # 50152011-14 (B-Blue-S) Serial # 31447408 (B-Green) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0632-2014%22
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