Integra Camino 110-4 Intracranial Pressure — Class II medical device recall Z-2072-2014
Terminated recall by Integra LifeSciences Corp., reported 2014-07-23. Integra LifeSciences is recalling the Camino Intracranial Pressure Monitoring Kits because of revised labellin
| Recall number | Z-2072-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp., Plainsboro, NJ, United States |
| Recall initiated | 2014-07-09 |
| Classified | 2014-07-17 |
| Reported by FDA | 2014-07-23 |
| Terminated | 2014-10-14 |
| Countries outside the US | AE, AR, AT, BE, BG, BR, CH, CL, CN, CY, DE, DZ, EG, ES, FI, FR, GB, GR, HU, IE, IL, IN, IT, JO, JP, KR, LB, LT, MX, NL, PL, PT, RO, SA, SE, SI, TN, TR, ZA |
| Quantity | 28,752 units |
| UPC / GTIN / UDI-DI | 00305000228523, 00305000229827, 00305000230304, 00305000231462, 00305000231714, 00305000232605, 00305000238263, 00305000250456, 00305000251453, 00305000267423, 00305000267676, 00305000272274 |
| Lot numbers | 305000222640, 305000223279, 305000223280, 305000223622, 305000223866, 305000223867, 305000223868, 305000224353, 305000224354, 305000225045, 305000225046, 305000225632, 305000225633, 305000225634, 305000226127, 305000226731, 305000226836, 305000226844, 305000226867, 305000227128, 305000227129, 305000228521, 305000228522, 305000228971, 305000229328, 305000229329, 305000229330, 305000229825, 305000229826, 305000230302, 305000230303, 305000230780, 305000230781, 305000231461, 305000231463, 305000232098, 305000232099, 305000232101, 305000232604, 305000232606 and 236 more |
| Model numbers | 110-4B, 110-4G, 110-4H, 110-4L |
Product
Integra Camino 110-4 Intracranial Pressure (ICP) Monitoring Catheters, Cat. No's. 110-4B, 110-4G, 110-4H, 110-4L
Reason for recall
Integra LifeSciences is recalling the Camino Intracranial Pressure Monitoring Kits because of revised labelling to indicate they are unsafe in an MR environment.
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-2072-2014. 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.