RecallRadar

FDA Device recall Z-2954-2020

Integra Padgett Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn tr…

On 2020-09-23 the FDA classified a Class II recall of Integra Padgett Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn tr… by Integra Lifesciences, citing lntegra LifeSciences has identified through a number of complaints that the handpiece cable melts following sterilization.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2954-2020
ClassificationClass II
Statusterminated
Initiated2020-08-04
Published2020-09-23
Last updated2026-09-13 11:55 UTC
CompanyIntegra Lifesciences
DistributionUS

Product

Integra Padgett Dermatome Set - Product Usage: are intended for use in the cutting of skin grafts for use in plastic surgery and/or burn treatment. These instruments are intended only for professional use in hospitals and similar medical facilities, where the patient will be under the supervision of trained personnel.

Reason

lntegra LifeSciences has identified through a number of complaints that the handpiece cable melts following sterilization.

Identifiers

code_info
Catalog Number: 3539700 Catalog Description: Slimline Dermatome Set Model #: S Lot/Serial #: S-1949, S-1919, S-1930…Catalog Number: 3539700 Catalog Description: Slimline Dermatome Set Model #: S Lot/Serial #: S-1949, S-1919, S-1930 to S-1932, S-1937 to S-1939, S-1944 to S-1946 ***Updated 5/3/21*** S-1927, S-1928

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-2954-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.