# FDA recall Z-1270-2020

> **TELEFLEX MEDICAL INC** · Class II · device recall initiated 2020-01-13.

## 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.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-1270-2020
- **Recalling firm:** TELEFLEX MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-01-13
- **Report date:** 2020-02-26
- **Termination date:** 2021-11-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1270-2020

## Citation

> AI Analytics. FDA recall Z-1270-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1270-2020. Source: US FDA. Licensed CC0.

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