Various Merit Medical convenience kits that contain recalled Jiangsu… — Class II medical device recall Z-2576-2024
Ongoing recall by Merit Medical Systems, Inc., reported 2024-08-21, distributed nationwide. Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. L
| Recall number | Z-2576-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merit Medical Systems, Inc., South Jordan, UT, United States |
| Recall initiated | 2024-06-11 |
| Classified | 2024-08-12 |
| Reported by FDA | 2024-08-21 |
| Distributed | Nationwide (US) |
| Quantity | 317,115 kits |
| Reason classes | packaging, device malfunction |
| UPC / GTIN / UDI-DI | 00884450038659, 00884450038673, 00884450038680, 00884450038697, 00884450038703, 00884450038710, 00884450038727, 00884450038734, 00884450038741, 00884450038758, 00884450038765, 00884450038772, 00884450277522, 00884450277546, 00884450277560, 00884450277577, 00884450277584, 00884450277591, 00884450277607, 00884450277645, 00884450277669, 00884450277737, 00884450277751, 00884450277775, 00884450277782 and 10 more |
| Lot numbers | SPPT-100/D, SPPT-5F-10/D, SPPT-5F-10L/B, SPPT-5F-10S, SPPT-5F-12PL, SPPT-5F-17PL, SPPT-5F-7/D, SPPT-5F-7L/B, SPPT-5F-7S, SPPT-6F-10L, SPPT-6F-10S, SPPT-6F-12PL, SPPT-6F-12PS, SPPT-6F-17PL, SPPT-8F-10L, SPPT-8F-12PL, T2319777, T2340050, T2351182, T2351183, T2351188, T2351191, T2351200, T2353607, T2365762, T2365767, T2365772, T2365801, T2367928, T2368460, T2379511, T2379512, T2379513, T2379520, T2379524, T2379527, T2379529, T2379531, T2379536, T2379537 and 460 more |
| Model numbers | SPPT-100/D, SPPT-5F-10/D, SPPT-5F-10L/B, SPPT-5F-10S, SPPT-5F-12PL, SPPT-5F-17PL, SPPT-5F-7/D, SPPT-5F-7L/B, SPPT-5F-7S, SPPT-6F-10L, SPPT-6F-10S, SPPT-6F-12PL, SPPT-6F-17PL, SPPT-8F-10L, SPPT-8F-12PL, TAPS-100, TAPS-5F-10LT, TAPS-5F-10T, TAPS-5F-12PLT, TAPS-5F-17PLT, TAPS-5F-7LT, TAPS-5F-7T, TAPS-6F-10LT |
Product
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Safety Paracentesis Procedure Tray (Paracentesis Tray kit), REF: SPPT-100/D SPPT-5F-10/D SPPT-5F-10L/B SPPT-5F-10S SPPT-5F-12PL SPPT-5F-17PL SPPT-5F-7/D SPPT-5F-7L/B SPPT-5F-7S SPPT-6F-10L SPPT-6F-10S SPPT-6F-10S SPPT-6F-12PL SPPT-6F-17PL SPPT-8F-10L SPPT-8F-12PL TAPS-100 TAPS-5F-10LT TAPS-5F-10T TAPS-5F-12PLT TAPS-5F-17PLT TAPS-5F-7LT TAPS-5F-7T TAPS-6F-10LT The Safety Paracentesis Procedure Tray is intended for drainage of fluid and specimen collection for diagnostic purposes or to remove excess fluid collections.
Reason for recall
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
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-2576-2024. 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.