FDA Device recall Z-2430-2012
Model 324JL On-Board Suction System Intended use: On-board suction system for Ambulance manufacturers
- FDA Device
- Class III
- terminated
- Published 2012-09-26
On 2012-09-26 the FDA classified a Class III recall of Model 324JL On-Board Suction System Intended use: On-board suction system for Ambulance manufacturers by Impact Instrumentation, citing A shipment mix-up took place.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2430-2012 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2012-03-30 |
| Published | 2012-09-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Impact Instrumentation |
| Distribution | US |
Product
Model 324JL On-Board Suction System Intended use: On-board suction system for Ambulance manufacturers.
Reason
A shipment mix-up took place.
Identifiers
| code_info | Model 324JL S/N 120142 and S/N 120144 |
|---|
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-2430-2012%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.