# FDA recall Z-1053-2020

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

## Product

Centurion- Laceration Trays  DYNDL1073	LACERATION TRAY  DYNDL1152A	LACERATION TRAY  DYNDL1152A	LACERATION TRAY  DYNDL1223A	LACERATION TRAY  DYNDL1295B	KIT,PAIN  DYNDL1436A	LACERATION TRAY  DYNDL1436A	LACERATION TRAY  DYNDL1600B	RCHSD CVP TRAY  DYNDL1606A	VAGINAL DELIVERY TRAY  DYNDL1617A	PICC INSERTION KIT-LATEX FREE  DYNDL1617A	PICC INSERTION KIT-LATEX FREE  DYNDL1630A	LACERATION TRAY  DYNDL1675	ARTHROGRAM TRAY  DYNDL1721	LACERATION TRAY  DYNDL1721	LACERATION TRAY  DYNDL1741A	LACERATION TRAY  DYNDL1744	LACERATION KIT  DYNDL1755	LACERATION TRAY  DYNDL1764A	LACERATION TRAY  DYNDL1772	LACERATION TRAY  DYNDL1772	LACERATION TRAY  DYNDL1786	SUTURING SET  DYNDL1790	LACERATION TRAY  DYNDL1796	LACERATION TRAY  DYNDL1812	PEDI LACERATION TRAY  DYNDL1840	SUTURE SET PACK  DYNDL1847	ER SUTURE TRAY  DYNDL1864A	LACERATION TRAY  DYNDL1897	LACERATION TRAY  DYNDL1897	LACERATION TRAY  DYNDL1920	LACERATION TRAY

## Reason for recall

Incomplete seals on the sterile package may compromise the sterility

## Distribution

Nationwide  Foreign: GHANA

## Key facts

- **Recall number:** Z-1053-2020
- **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-1053-2020

## Citation

> AI Analytics. FDA recall Z-1053-2020. Retrieved 2026-06-22 from https://api.ai-analytics.org/recall/Z-1053-2020. Source: US FDA. Licensed CC0.

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