US Endoscopy Padlock Clip defect closure system Ref: C910001 The… — Class II medical device recall Z-1011-2019
Terminated recall by US Endoscopy Group Inc, reported 2019-03-20, distributed nationwide. Potential esophageal laceration during a patient procedure
| Recall number | Z-1011-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | US Endoscopy Group Inc, Mentor, OH, United States |
| Recall initiated | 2019-02-04 |
| Classified | 2019-03-13 |
| Reported by FDA | 2019-03-20 |
| Terminated | 2020-08-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BE, CZ, DE, ES, GB, IN, IT, KR, LB, MX, NL, NO, PH, SE |
| Lot numbers | 1814568, 1814569, 1815200, 1815592, 1816056, 1817174, 1817810, 1818187, 1818596, 1819180, 1819181, 1819407, 1819793, 1820177 |
| Model numbers | C910001 |
Product
US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs.
Reason for recall
Potential esophageal laceration during a patient procedure
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-1011-2019. 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.