Cook Lead Clipper- An auxiliary tool indicated for use in patients… — Class II medical device recall Z-2513-2023
Ongoing recall by Cook Vandergrift, Inc., reported 2023-09-13, distributed nationwide. Sterility of device may be compromised due to breach of the chevron seal of the packaging
| Recall number | Z-2513-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Vandergrift, Inc., Vandergrift, PA, United States |
| Recall initiated | 2023-07-24 |
| Classified | 2023-09-01 |
| Reported by FDA | 2023-09-13 |
| Distributed | Nationwide (US) |
| Quantity | 15,951 |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 00827002200036 |
| Lot numbers | N172707, N172737, N172738, N172875, N172887, N172912, N173153, N173178, N173180, N173434, N173519, N173623, N173653, N173688, N173690, N173691, N173879, N173943, N173959, N173976, N173977, N174034, N174104, N174134, N174169, N174170, N174287, N174294, N174466, N174535, N174536, N174564, N174589, N174704, N174778, N174841, N174863, N174864, N174889, N174906 and 318 more |
| Model numbers | LR-CLP001 |
Product
Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous retrieval of cardiac leads. Order Number (GPN): G20003 Reference Part Number (RPN): LR-CLP001
Reason for recall
Sterility of device may be compromised due to breach of the chevron seal of the packaging
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-2513-2023. 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.