RecallRadar

FDA Device recall Z-1453-2015

Talon Grasping Device, 160 cm, US endoscopy

On 2015-04-22 the FDA classified a Class II recall of Talon Grasping Device, 160 cm, US endoscopy by Us Endoscopy Group, citing A wire component on the distal grasping assembly of the device became detached.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1453-2015
ClassificationClass II
Statusterminated
Initiated2015-03-10
Published2015-04-22
Last updated2026-09-13 11:53 UTC
CompanyUs Endoscopy Group
DistributionAL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV

Product

Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract.

Reason

A wire component on the distal grasping assembly of the device became detached..

Identifiers

code_info
Model #00711175; Lot #'s: 1407418, 1407419, 1408069, 1408070, 1408739, 1408740, 1408741, 1408742, 1410178, 1410179, 141…Model #00711175; Lot #'s: 1407418, 1407419, 1408069, 1408070, 1408739, 1408740, 1408741, 1408742, 1410178, 1410179, 1410478, 1410480, 1410990, 1411518, 1423937, and 1423938.

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-1453-2015%22

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