RecallRadar

FDA Device recall Z-2658-2015

BASIC PACK 8/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, ir…

On 2015-09-09 the FDA classified a Class II recall of BASIC PACK 8/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, ir… by Customed, citing recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2658-2015
ClassificationClass II
Statusterminated
Initiated2015-07-10
Published2015-09-09
Last updated2026-09-13 11:53 UTC
CompanyCustomed
DistributionPR

Product

BASIC PACK 8/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

Reason

Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Identifiers

code_info
Code:9002829 Lots: 140915330 exp. 2/28/16 141015714 exp. 11/30/15 141216444 exp. 12/31/15 150116707 exp. 1/31/16…Code:9002829 Lots: 140915330 exp. 2/28/16 141015714 exp. 11/30/15 141216444 exp. 12/31/15 150116707 exp. 1/31/16 150116943 exp. 2/28/16 150317648 exp. 3/31/16 150318092 exp. 3/31/16 150418386 exp. 4/30/16 150418509 exp. 4/30/16 150418509 exp. 4/30/16 150619180 exp. 6/30/16 150619181 exp. 6/30/16

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2658-2015%22

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