Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The… — Class II medical device recall Z-0922-2013
Terminated recall by Instratek, Incorporated, reported 2013-03-20, distributed nationwide. Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger Release Blades which could not be a
| Recall number | Z-0922-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Instratek, Incorporated, Houston, TX, United States |
| Recall initiated | 2012-09-18 |
| Classified | 2013-03-08 |
| Reported by FDA | 2013-03-20 |
| Terminated | 2013-04-10 |
| Distributed | Nationwide (US) |
| Quantity | 235 |
| Lot numbers | M674180, M674200, MAKL170 |
| Model numbers | 1052 |
Product
Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release procedures.
Reason for recall
Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger Release Blades which could not be advanced into the cannula through which it is used during trigger finger release procedures.
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-0922-2013. 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.