FDA recall record

Deroyal Industries, Inc. Lafollette Teleflex Pilling Aortic Punch, 4.0mm recall — FDA Z-1483-2020

The sterile packaging has the potential to be compromised.

Class IIclassification
Z-1483-2020official record ID
Mar 25, 2020report date

Recall record at a glance

Official recordZ-1483-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDeroyal Industries, Inc. Lafollette
Report dateMar 25, 2020
Recall initiation dateFeb 6, 2020
Quantity669 units
LocationLa Follette, TN, United States

Official 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.

Why the product was recalled

The sterile packaging has the potential to be compromised.

Distribution information

International distribution of Kuwait City, Kuwait.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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