FDA Device recall Z-2701-2015

CARPAL TUNEL LARGE SURGICAL PACK, 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound heali…

FDA Device
Class II
terminated
Published 2015-09-09

On 2015-09-09 the FDA classified a Class II recall of CARPAL TUNEL LARGE SURGICAL PACK, 6/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound heali… 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

Agency	FDA Device
Recall number	Z-2701-2015
Classification	Class II
Status	terminated
Initiated	2015-07-10
Published	2015-09-09
Last updated	2026-09-13 11:53 UTC
Company	Customed
Distribution	PR

Product

CARPAL TUNEL LARGE SURGICAL PACK, 6/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:900742A Lots: 141015498 exp. 1/31/16 141216361 exp. 12/31/15 150116507 exp. 12/31/15 141216450 exp. 1/31/16… Code:900742A Lots: 141015498 exp. 1/31/16 141216361 exp. 12/31/15 150116507 exp. 12/31/15 141216450 exp. 1/31/16 150317875 exp. 3/31/16 150317876 exp. 3/31/16 150418421 exp. 4/30/16 150518841 exp. 5/31/16 150619190 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-2701-2015%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.