Deroyal Industries, Inc. Lafollette: Medical Device Recall in 2020 - (Recall #: Z-1483-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: February 6, 2020

Date Posted: March 25, 2020

Recall Number: Z-1483-2020

Event ID: 84943

Reason for Recall:

The sterile packaging has the potential to be compromised.

Status: Terminated

Product Quantity: 669 units

Code Information:

Catalog Number DP40K; Lot Numbers: 74F1802710, 74G1802678, 74H1800763, 74D1900657, 74C1900811, 74D1700564

Distribution Pattern:

International distribution of Kuwait City, Kuwait.

Voluntary or Mandated:

Voluntary: Firm initiated