Teleflex Medical Disposable Aortic Punch — Class II medical device recall Z-1270-2020
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-1270-2020 |
|---|---|
| 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 | 587,066 units |
| Reason classes | sterility |
| Lot numbers | 74A1500172, 74A1500226, 74A1501140, 74A1501142, 74A1501146, 74A1501148, 74A1501153, 74A1502433, 74A1502434, 74A1502835, 74A1502836, 74A1502837, 74A1502848, 74A1502850, 74A1502851, 74A1502852, 74A1503439, 74A1503453, 74A1601248, 74A1601249, 74A1601250, 74A1601251, 74A1601252, 74A1601253, 74A1601254, 74A1601255, 74A1601256, 74A1601257, 74A1601258, 74A1601259, 74A1601260, 74A1602049, 74A1602178, 74A1602179, 74A1602180, 74A1602181, 74A1602182, 74A1602183, 74A1602184, 74A1602185 and 460 more |
| Model numbers | DP-28K, DP-36K, DP-40K, DP-44K, DP-48K, DP-52K, DP-56K, DP-60K, MDP-28K, MDP-36K, MDP-40K, MDP-44K, MDP-48K, MDP-52K, MDP-56K, MDP-60K |
Product
Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF DP-28K b) 3.6 mm, REF DP-36K c) 4.0 mm, REF DP-40K d) 4.4 mm, REF DP-44K e) 4.8 mm, REF DP-48K f) 5.2 mm, REF DP-52K g) 5.6 mm, REF DP-56K h) 6.0 mm, REF DP-60K i) 2.8 mm, REF MDP-28K j) 3.6 mm, REF MDP-36K k) 4.0 mm, REF MDP-40K l) 4.4 mm, REF MDP-44K m) 4.8 mm, REF MDP-48K n) 5.2 mm, REF MDP-52K o) 5.6 mm, REF MDP-56K p) 6.0 mm, REF MDP-60K
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-1270-2020. 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.