RecallRadar

FDA Device recall Z-2627-2015

SURGICAL PACK 20/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals…

On 2015-09-09 the FDA classified a Class II recall of SURGICAL PACK 20/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals… 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-2627-2015
ClassificationClass II
Statusterminated
Initiated2015-07-10
Published2015-09-09
Last updated2026-09-13 11:53 UTC
CompanyCustomed
DistributionPR

Product

SURGICAL PACK 20/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:9002224 Lots: 141015709 exp. 2/28/16 141216301 exp. 12/31/15 150116523 exp. 1/31/16 150116524 exp. 1/31/16 1…Code:9002224 Lots: 141015709 exp. 2/28/16 141216301 exp. 12/31/15 150116523 exp. 1/31/16 150116524 exp. 1/31/16 150116525 exp. 1/31/16 150116526 exp. 1/31/16 150317725 exp. 4/30/16 150317726 exp. 4/30/16 150418352 exp. 4/30/16 150418351 exp. 4/30/16 150518686 exp. 5/31/16 150518687 exp. 5/31/16 150519027 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-2627-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.