Data Foundry

Medical device recalls 2024

SURG STRP 1/2X6 Model/Catalog Number: 801451 — Class II medical device recall Z-0250-2025

Ongoing recall by Integra LifeSciences Corp., reported 2024-11-06, distributed nationwide. Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Pa

Recall numberZ-0250-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmIntegra LifeSciences Corp., Princeton, NJ, United States
Recall initiated2024-09-20
Classified2024-10-29
Reported by FDA2024-11-06
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BB, BE, BG, BH, BO, BR, BS, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DO, EC, ES, FR, GB, GH, GR, HK, HU, IE, IL, IQ, IS, IT, JO, JP, KE, KR, KW, LB, LT, LU, MA, MT, MX, MY, NG, NL, NZ, OM, PA, PE, PH, PK, PL, PT, QA, RO, RS, SA, SE, SG, SI, SV, TR, TT, TW, ZA
Reason classessterility
UPC / GTIN / UDI-DI10381780515074, 20886704036590
Model numbers801451

Product

SURG STRP 1/2X6 Model/Catalog Number: 801451. The surgical patties and surgical strips are indicated for the use in protection of tissue, including brain and other tissues of the central nervous system, during surgery.

Reason for recall

Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in finished goods

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-0250-2025. 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.