# FDA recall Z-1052-2020

> **Centurion Medical Products Corporation** · Class II · device recall initiated 2019-12-11.

## Product

Centurion-General Surgery Convenience Kits  DYNDH1033B	SUBCLAVIAN ON/OFF KIT  DYNDH1090A	SDS PROCEDURE PACK  DYNDH1110	BIOPSY PACK  DYNDH1110	BIOPSY PACK  DYNDH1110	BIOPSY PACK  DYNDH1114	BIOPSY TRAY  DYNDH1131	WDC ULTRASOUND KIT  DYNDH1227A	HOLSTON MYELOGRAM PACK  DYNDH1227A	HOLSTON MYELOGRAM PACK  DYNDH1265	MYELOGRAM TRAY  DYNDH1272	LUMBAR PUNCTURE TRAY  DYNDH1281A	PARA/THORA ULTRASOUND  DYNDH1285A	BIOPSY ULTRASOUND  DYNDH1321	LUMBAR PUNCTURE TRAY  DYNDH1349	ARTHROGRAM TRAY  DYNDH1359	DIAGNOSTIC TRAY  DYNDH1397	GENERAL ASPIRATION TRAY - CHOICE  DYNDH1399	ARTHROGRAM TRAY

## Reason for recall

Incomplete seals on the sterile package may compromise the sterility

## Distribution

Nationwide  Foreign: GHANA

## Key facts

- **Recall number:** Z-1052-2020
- **Recalling firm:** Centurion Medical Products Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-11
- **Report date:** 2020-02-12
- **Termination date:** 2020-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Williamston, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1052-2020

## Citation

> AI Analytics. FDA recall Z-1052-2020. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1052-2020. Source: US FDA. Licensed CC0.

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