# FDA recall Z-1646-2023

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2023-04-21.

## Product

Procedure packs:    (1) Medline Sterile Arthroscopy Pack, REF: DYNJ64242B;  (2) Medline Sterile Shoulder Pack, REF: DYNJ64250A; and  (3) Medline Sterile Upper Extremity Pack, REF: DYNJ64253B.

## Reason for recall

The kits were damaged by water.

## Distribution

Distribution was made to California.  There was no foreign/government/military distribution.

## Key facts

- **Recall number:** Z-1646-2023
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-21
- **Report date:** 2023-06-07

- **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-1646-2023

## Citation

> AI Analytics. FDA recall Z-1646-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1646-2023. Source: US FDA. Licensed CC0.

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