Pilling Aortic Punch — Class II medical device recall Z-1269-2020
Terminated recall by TELEFLEX MEDICAL INC, reported 2020-02-26. There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot
| Recall number | Z-1269-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX MEDICAL INC, Morrisville, NC, United States |
| Recall initiated | 2020-01-13 |
| Classified | 2020-02-19 |
| Reported by FDA | 2020-02-26 |
| Terminated | 2021-11-24 |
| Quantity | 1,764 units |
| Reason classes | sterility |
| Lot numbers | 74B1500674 |
| Model numbers | 353440 |
Product
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Reason for recall
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
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-1269-2020. 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.