Model 324JL On-Board Suction System Intended use: On-board suction… — Class III medical device recall Z-2430-2012
Terminated recall by Impact Instrumentation, Inc., reported 2012-09-26, distributed nationwide. A shipment mix-up took place.
| Recall number | Z-2430-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Impact Instrumentation, Inc., West Caldwell, NJ, United States |
| Recall initiated | 2012-03-30 |
| Classified | 2012-09-20 |
| Reported by FDA | 2012-09-26 |
| Terminated | 2015-07-21 |
| Distributed | Nationwide (US) |
| Quantity | 2 devices |
| Model numbers | 120142, 120144, 324JL |
Product
Model 324JL On-Board Suction System Intended use: On-board suction system for Ambulance manufacturers.
Reason for recall
A shipment mix-up took place.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2430-2012. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.