# FDA recall Z-0765-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class I · device recall initiated 2024-12-16.

## Product

Medline Fluid Delivery Set with Drip Chamber:    1) MTO,135,YELLOW,MICRO,SPK-MAIMONIDES, Item Number: 60130527;  2) MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH, Item Number: 65111341;  3) MTO,ANGIO,SINGLE,SPIKE,KIT, Item Number: 65232486;  4) MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM, Item Number: 65071193;  5) MTO,NEURO,FLUSH,SPIKE,KIT,BLUE,FLORIDA, Item Number: 600604422;  6) MTO,NEURO,KIT,-,JERSEY,SHORE  PG, Item Number: 60100045;  7) MTO,RADIOLOGY,KIT,HAMOT MED CEN, Item Number: 650801715;  8) MTS,135,CDS,IV,TUBE-JEFFERSON UNIV., Item Number: 60232481;  9) MTS,135,YELLOW,MICRO,SPIKE,LUTHERAN MED, Item Number: 60120583;  10) MTS,ANGIO,NEURO,KIT,NORTH SHORE  UNIV, Item Number: 601403920;  11) MTS,CUST. FILTER-NEWYORK UNIVERSITY, Item Number: 62140602;  12) MTS,INTERV,NEURO,KIT-WESTCHESTER,MC, Item Number: 602301614;  13) MTS,NEU,NORTH SHORE HOSPITAL, Item Number: 6010771601;  14) MTS,NEURO,KIT, Item Number: 600602914;  15) MTS,NEURO,KIT,2,NEWENGLAND MED CTR, Item Number: 601400111;  16) MTS,NE

## Reason for recall

Fluid Delivery Sets were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber. The macro drip chamber delivers three times more fluid per drop than the micro drip chamber.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-0765-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-16
- **Report date:** 2025-01-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0765-2025

## Citation

> AI Analytics. FDA recall Z-0765-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0765-2025. Source: US FDA. Licensed CC0.

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