RecallRadar

FDA Device recall Z-0246-2015

Surgeon Gown Poly Reinforced Lgc, Catalog number 900-522

On 2014-12-10 the FDA classified a Class I recall of Surgeon Gown Poly Reinforced Lgc, Catalog number 900-522 by Customed, citing customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncont….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0246-2015
ClassificationClass I
Statusterminated
Initiated2014-10-08
Published2014-12-10
Last updated2026-09-13 11:53 UTC
CompanyCustomed
DistributionFL, NY, PR

Product

Surgeon Gown Poly Reinforced Lgc, Catalog number 900-522. Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

Reason

Customed products are being recalled because of compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.

Identifiers

code_info
Lot numbers: 111103265 111113126 112010183 112020505 112030804 112041056 112051993 112072804 112093631 112104…Lot numbers: 111103265 111113126 112010183 112020505 112030804 112041056 112051993 112072804 112093631 112104361 112104533 112124897 113026196 113036804 113057491 113067873 113078333 113088873 113099438 113109852 131110265 131210654 140111126 140211540 140312173 140312384 140513370 140714295 140814813 140814957 140915481

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-0246-2015%22

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