AMS-530 7 Microbore Trifurcated Extension sets Product Usage:… — Class II medical device recall Z-0813-2014
Terminated recall by Churchill Medical Systems, Inc., reported 2014-01-29, distributed nationwide. Defective component may cause extension sets to leak.
| Recall number | Z-0813-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Churchill Medical Systems, Inc., Dover, NH, United States |
| Recall initiated | 2014-01-07 |
| Classified | 2014-01-23 |
| Reported by FDA | 2014-01-29 |
| Terminated | 2014-11-03 |
| Distributed | Nationwide (US) |
| Quantity | 3,850 |
| Reason classes | packaging |
| Lot numbers | 1306034, 1307011 |
Product
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
Reason for recall
Defective component may cause extension sets to leak.
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-0813-2014. 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.