# FDA recall Z-1476-2022

> **MEDLINE INDUSTRIES, LP - SPT** · Class II · device recall initiated 2022-06-06.

## Product

Medline Custom procedural kits labeled as follows:  a. GP-NEURO PACK, b. KIT NEUR FUS LUM POST, c. KIT PEDI VP SHUNT, d. KIT STC NEURO SPINE GENERIC, e. MAIN BASIC NEURO, f. MAJOR NEURO PK-LF, g. NEURO, h. NEURO CERVICAL PACK, i. NINOR NEURO PK-LF, j. VP SHUNT PACK  Model/Catalog Number: Model Numbers:  a.DYNJ0397191V, b. DYKMBNDL138, c. DYNJ907374, d. DYKMBNDL40A, e. DYNJ908260, f. DYNJ21243M, g. DYNJ904818D,  DYNJ905194,  DYNJ904040D,  DYNJ904040F,  DYNJ904818C,  DYNJ905753A, h. DYNJ0101287I, i. DYNJ21244N, j. DYNJ46530J

## Reason for recall

Kits contain leaking bottles of isopropyl alcohol

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1476-2022
- **Recalling firm:** MEDLINE INDUSTRIES, LP - SPT
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-06
- **Report date:** 2022-08-03

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1476-2022

## Citation

> AI Analytics. FDA recall Z-1476-2022. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-1476-2022. Source: US FDA. Licensed CC0.

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