Data Foundry

Medical device recalls 2013

Torrent" irrigation tubing — Class II medical device recall Z-1099-2013

Terminated recall by US Endoscopy Group Inc, reported 2013-04-17, distributed nationwide. The firm was notified by their customers that there was a water leakage from the white tubing connector.

Recall numberZ-1099-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmUS Endoscopy Group Inc, Mentor, OH, United States
Recall initiated2013-03-07
Classified2013-04-11
Reported by FDA2013-04-17
Terminated2014-03-20
DistributedNationwide (US)
Quantity21,189 units
Reason classespackaging
Lot numbers79687, 79688, 79689, 79690, 79691, 79692, 79693, 79694, 79695, 79696, 80165, 80166, 80709, 80710, 80711, 80712, 80713, 80714, 80715, 80716, 80717, 80718, 80719, 80720, 80721, 80722, 80723, 81245, 81246, 81247, 81248, 81249, 81250, 81251, 81252, 81253, 81254, 81255, 81256, 81257 and 48 more

Product

Torrent" irrigation tubing. Product Usage: The Torrent irrigation system (tubing and accessories to accommodate various endoscopes and irrigation pumps) is intended to provide irrigation via irrigation fluids, such as sterile water, during gastrointestinal endoscopic procedures when used in conjunction with an irrigation pump or electrosurgical unit.

Reason for recall

The firm was notified by their customers that there was a water leakage from the white tubing connector.

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-1099-2013. 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.