Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 — Class II medical device recall Z-1222-2017
Terminated recall by Atrium Medical Corporation, reported 2017-02-22, distributed nationwide. Labeling icon depicts a catheter having six (6) eyelets; however the correct number of eyelets on the 8 Fr and
| Recall number | Z-1222-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atrium Medical Corporation, Hudson, NH, United States |
| Recall initiated | 2017-01-20 |
| Classified | 2017-02-16 |
| Reported by FDA | 2017-02-22 |
| Terminated | 2020-11-03 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
Product
Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010
Reason for recall
Labeling icon depicts a catheter having six (6) eyelets; however the correct number of eyelets on the 8 Fr and 10 Fr thoracic catheters is two (2)
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-1222-2017. 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.