VERITAS Advanced Infusion Packs — Class II medical device recall Z-2247-2023
Ongoing recall by Johnson & Johnson Surgical Vision, Inc., reported 2023-08-09, distributed nationwide. Weld protrusion/physical gap between the housing and pack cover, may exceed design specification, due to a man
| Recall number | Z-2247-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Johnson & Johnson Surgical Vision, Inc., Irvine, CA, United States |
| Recall initiated | 2023-05-30 |
| Classified | 2023-07-28 |
| Reported by FDA | 2023-08-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BG, BR, CA, CH, CL, CN, CZ, DE, DK, EC, EE, EG, ES, FI, FR, GB, GR, HK, ID, IL, IN, IQ, IT, JO, JP, KR, KW, LB, MA, MY, NL, NO, NZ, OM, PE, PL, PT, SA, SE, SG, TH, TR, TW, VE, ZA |
| Quantity | 148,941 |
| UPC / GTIN / UDI-DI | 05050474700895, 05050474700901 |
| Lot numbers | 60302489, 60302939, 60302941, 60302953, 60302954, 60304170, 60304173, 60304174, 60304175, 60304176, 60305657, 60305658, 60305659, 60305660, 60305661, 60305662, 60305665, 60306930, 60306931, 60306932, 60306933, 60306934, 60306935, 60306936, 60306940, 60306942, 60308189, 60308190, 60308193, 60309844, 60309845, 60309847, 60309848, 60309850, 60309853, 60314640, 60314641, 60314642, 60314674, 60314675 and 58 more |
Product
VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
Reason for recall
Weld protrusion/physical gap between the housing and pack cover, may exceed design specification, due to a manufacturing issue, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.
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-2247-2023. 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.