Avid Medical, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0793-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

AVID TruCustom LOWER EXTREMITY convenience kits, Item Code: LGHM038-03 and LGHM038-04

Product Classification:

Class II

Date Initiated: June 22, 2017

Date Posted: March 7, 2018

Recall Number: Z-0793-2018

Event ID: 79162

Reason for Recall:

Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.

Status: Terminated

Product Quantity: 120

Code Information:

Lot, Expiration Date: 1207468, 9/1/2019; 1216677, 9/1/2019; 1221264, 9/20/2019; 1222553, 9/1/2019

Distribution Pattern:

Distributed in 10 states: IL, KY, LA, MA, MO, NY, OH, TX, VA, WI.

Voluntary or Mandated:

Voluntary: Firm initiated