Data Foundry

Medical device recalls 2015

Talon Grasping Device — Class II medical device recall Z-1453-2015

Terminated recall by US Endoscopy Group Inc, reported 2015-04-22, distributed in AL, AR, AZ, CA, CO, CT, DC, FL…. A wire component on the distal grasping assembly of the device became detached..

Recall numberZ-1453-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmUS Endoscopy Group Inc, Mentor, OH, United States
Recall initiated2015-03-10
Classified2015-04-16
Reported by FDA2015-04-22
Terminated2016-10-27
DistributedAL, 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
Countries outside the USAR, AU, BE, CA, EE, FR, MX, NZ, SA, SE
Quantity1,695 units
Reason classesdevice malfunction
Lot numbers1407418, 1407419, 1408069, 1408070, 1408739, 1408740, 1408741, 1408742, 1410178, 1410179, 1410478, 1410480, 1410990, 1411518, 1423937, 1423938
Model numbers00711175

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 for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1453-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.