RecallRadar

FDA Device recall Z-0266-2019

CHS Custom Convenience (1) 1231-150L GOWN, RAGLAN, LG, NONREINF (2) 1231-150XL GOWN, RAGLAN, XL, NONREINF (3) 1231-140XL GOWN, SPECIALTY XL…

On 2018-10-31 the FDA classified a Class II recall of CHS Custom Convenience (1) 1231-150L GOWN, RAGLAN, LG, NONREINF (2) 1231-150XL GOWN, RAGLAN, XL, NONREINF (3) 1231-140XL GOWN, SPECIALTY XL… by Custom Healthcare Systems, citing convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0266-2019
ClassificationClass II
Statusterminated
Initiated2018-08-13
Published2018-10-31
Last updated2026-09-13 11:54 UTC
CompanyCustom Healthcare Systems
DistributionCT, GA, IL, KY, MD, NC, OK, SC, VA

Product

CHS Custom Convenience (1) 1231-150L GOWN, RAGLAN, LG, NONREINF (2) 1231-150XL GOWN, RAGLAN, XL, NONREINF (3) 1231-140XL GOWN, SPECIALTY XL, XLONG

Reason

Convenience kits were sealed in immediate Tyvek pouches using incorrect specifications compromising product sterility

Identifiers

code_info
(1)1231-150L GOWN, RAGLAN, LG, NONREINF Lot Numbers: W72318,W72118 (2) 1231-150XL GOWN, RAGLAN, XL, NONREINF Lot Nu…(1)1231-150L GOWN, RAGLAN, LG, NONREINF Lot Numbers: W72318,W72118 (2) 1231-150XL GOWN, RAGLAN, XL, NONREINF Lot Number: W72318 (3) 1231-140XL GOWN, SPECIALTY XL, XLONG Lot Number: W71818 Exp. Date: 7/1/2021

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0266-2019%22

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