FDA Device recall Z-2061-2014
ACL TOP 700, automated coagulation laboratory instrument
- FDA Device
- Class II
- terminated
- Published 2014-07-23
On 2014-07-23 the FDA classified a Class II recall of ACL TOP 700, automated coagulation laboratory instrument by Instrumentation Laboratory, citing potential for sample misidentification.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2061-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-03 |
| Published | 2014-07-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Instrumentation Laboratory |
| Distribution | US |
Product
ACL TOP 700, automated coagulation laboratory instrument.
Reason
Potential for sample misidentification.
Identifiers
| code_info | Start SN and Date: 09080100 Aug 2009 and End SN and Date 14050732 May 2014 |
|---|
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-2061-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.