Rochester-Pean Hemostatic Forceps 61/4 — Class II medical device recall Z-0751-2017
Terminated recall by Integra York PA, Inc, reported 2016-12-21, distributed in NC, TX. The Chevron seals of 6x10 Tyvek peel pouch used to package the sterile instruments may separate causing the pa
| Recall number | Z-0751-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra York PA, Inc, York, PA, United States |
| Recall initiated | 2016-10-28 |
| Classified | 2016-12-13 |
| Reported by FDA | 2016-12-21 |
| Terminated | 2017-04-17 |
| Distributed | NC, TX |
| Quantity | 150 units |
| Reason classes | sterility |
| Lot numbers | 352 |
| Model numbers | ST7-138 |
Product
Rochester-Pean Hemostatic Forceps 61/4, Curved, Sterile. The Rochester-Pean Hemostatic Forceps 61/4 Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.
Reason for recall
The Chevron seals of 6x10 Tyvek peel pouch used to package the sterile instruments may separate causing the packages to open and compromise sterility of the instrument.
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-0751-2017. 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.