Data Foundry

Medical device recalls 2024

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 numberZ-2576-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMerit Medical Systems, Inc., South Jordan, UT, United States
Recall initiated2024-06-11
Classified2024-08-12
Reported by FDA2024-08-21
DistributedNationwide (US)
Quantity317,115 kits
Reason classespackaging, device malfunction
UPC / GTIN / UDI-DI00884450038659, 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 numbersSPPT-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 numbersSPPT-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.