RecallRadar

FDA Device recall Z-2699-2015

ARTHROSCOPY SURGICAL PACK 4/C Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, sutur…

On 2015-09-09 the FDA classified a Class II recall of ARTHROSCOPY SURGICAL PACK 4/C Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, sutur… 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-2699-2015
ClassificationClass II
Statusterminated
Initiated2015-07-10
Published2015-09-09
Last updated2026-09-13 11:53 UTC
CompanyCustomed
DistributionPR

Product

ARTHROSCOPY SURGICAL PACK 4/C 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:900740A Lots: 140915497 exp. 1/31/16 141216360 exp. 12/31/15 141216449 exp. 1/31/16 141216449 exp. 1/31/16 1…Code:900740A Lots: 140915497 exp. 1/31/16 141216360 exp. 12/31/15 141216449 exp. 1/31/16 141216449 exp. 1/31/16 150317655 exp. 3/31/16 150317656 exp. 3/31/16 150318093 exp. 3/31/16 150418420 exp. 4/30/16 150518838 exp. 5/31/16 150619188 exp. 6/30/16 150619405 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-2699-2015%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.