FDA Device recall Z-0813-2014
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set
- FDA Device
- Class II
- terminated
- Published 2014-01-29
On 2014-01-29 the FDA classified a Class II recall of AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set by Churchill Medical Systems, citing defective component may cause extension sets to leak.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0813-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-01-07 |
| Published | 2014-01-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Churchill Medical Systems |
| Distribution | US |
Product
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
Reason
Defective component may cause extension sets to leak.
Identifiers
| code_info | Lot Number: 1306034, 1307011 |
|---|
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-0813-2014%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.