# FDA recall Z-1470-2022

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

## Product

Medline Convenience kits labeled as follows:  a. BEDSIDE PICC CDS, Model Number CDS984642, b. VASCULAR CDS, Model Number DYNJ902880J, c. VASCULAR CDS, Model Number DYNJ902880K, d. OPEN HEART A & B, Model Number DYNJ904831F, e. OPEN HEART MHS, Model Number DYNJ905394A, f. OPEN HEART MHS, Model Number DYNJ905394B, g. OPEN HEART WPH, Model Number DYNJ908168  Model/Catalog Number: Model Numbers:  a.  CDS984642, b.  DYNJ902880J, c.  DYNJ902880K, d.  DYNJ904831F, e.  DYNJ905394A, f.  DYNJ905394B, g.  DYNJ908168  Product Description: convenience kits labeled as follows:

## Reason for recall

Kits contain leaking bottles of isopropyl alcohol

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1470-2022
- **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-1470-2022

## Citation

> AI Analytics. FDA recall Z-1470-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1470-2022. Source: US FDA. Licensed CC0.

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