Teleflex Pilling Aortic Punch — Class II medical device recall Z-1483-2020
Terminated recall by Deroyal Industries, Inc. Lafollette, reported 2020-03-25. The sterile packaging has the potential to be compromised.
| Recall number | Z-1483-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Deroyal Industries, Inc. Lafollette, La Follette, TN, United States |
| Recall initiated | 2020-02-06 |
| Classified | 2020-03-13 |
| Reported by FDA | 2020-03-25 |
| Terminated | 2021-02-11 |
| Countries outside the US | KW |
| Quantity | 669 units |
| Reason classes | sterility |
| Lot numbers | 74C1900811, 74D1700564, 74D1900657, 74F1802710, 74G1802678, 74H1800763 |
| Model numbers | DP40K |
Product
Teleflex Pilling Aortic Punch, 4.0mm. Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit - Product Usage: This device is used for cardiovascular surgical procedures.
Reason for recall
The sterile packaging has the potential to be compromised.
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-1483-2020. 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.