RecallRadar

FDA Device recall Z-0656-2020

Ligamax 5 mm Endoscopic Multiple Clip Applier

On 2019-12-18 the FDA classified a Class II recall of Ligamax 5 mm Endoscopic Multiple Clip Applier by Ethicon Endo Surgery, citing A potential exists that certain LIGAMAX devices within the impacted lots may have small holes in the Tyvek lidding which could result in a breach of sterility.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0656-2020
ClassificationClass II
Statusterminated
Initiated2019-11-07
Published2019-12-18
Last updated2026-09-13 11:55 UTC
CompanyEthicon Endo Surgery
DistributionUS

Product

Ligamax 5 mm Endoscopic Multiple Clip Applier

Reason

A potential exists that certain LIGAMAX devices within the impacted lots may have small holes in the Tyvek lidding which could result in a breach of sterility.

Identifiers

code_info
Product Code: 11EL5ML Lot Numbers: T93X4R, T93X9D, T93Y2Z, T93Y70, T93Y96, T93Z52, T93Z76, T9401C, T9408F, T94118, T94…Product Code: 11EL5ML Lot Numbers: T93X4R, T93X9D, T93Y2Z, T93Y70, T93Y96, T93Z52, T93Z76, T9401C, T9408F, T94118, T9416M, T9422K, T9426Z, T94402, T94536, T94567, T9461M, T94667, T94721, T94758, T94807, T9484Y, T9487J, T9491A T94A9K, T94C2Z, T94C8N, T94D2N, T94E66, T94F3C, T94F7F, T94G99 T94H1N, T94H78

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-0656-2020%22

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