FDA Device recall Z-1483-2020
Teleflex Pilling Aortic Punch, 4.0mm
- FDA Device
- Class II
- terminated
- Published 2020-03-25
On 2020-03-25 the FDA classified a Class II recall of Teleflex Pilling Aortic Punch, 4.0mm by Deroyal Industries Lafollette, citing the sterile packaging has the potential to be compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1483-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-02-06 |
| Published | 2020-03-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Deroyal Industries Lafollette |
| Distribution | n/a |
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
The sterile packaging has the potential to be compromised.
Identifiers
| code_info | Catalog Number DP40K; Lot Numbers: 74F1802710, 74G1802678, 74H1800763, 74D1900657, 74C1900811, 74D1700564 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1483-2020%22
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