# FDA recall Z-1057-2020

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

## Product

Centurion-Suture Trays  SUT10140	SUTURE TRAY  SUT10290	LACERATION TRAY  SUT10705	SUTURING TRAY  SUT10770	DEBRIDEMENT/SUTURE SET  SUT10795	PORT IMPLANT SET  SUT11035	SUTURE TRAY  SUT11065	LACERATION TRAY  SUT1113A	SUTURING SET  SUT11145	SNAGFREE SUTURE SET W/SURGICAL INST.  SUT11515	LACERATION TRAY  SUT11540A	LACERATION TRAY  SUT11590	SUTURE SET  SUT11775	LACERATION TRAY  SUT11780	MINOR TRAY  SUT1189B	LACERATION TRAY  SUT11900	SUTURE TRAY  SUT11910	LACERATION TRAY  SUT11965	SUTURE SET  SUT11970	SUTURE TRAY  SUT12025	LACERATION TRAY  SUT12225	SUTURE TRAY REGULAR  SUT12275	SUTURING SET  SUT12335	LACERATION TRAY  SUT12625	SNAGFREE LACERATION TRAY  SUT12765	SNAGFREE LACERATION TRAY  SUT12895	SUTURE SET  SUT12895	SUTURE SET  SUT12895	SUTURE SET  SUT12970	PLASTIC TRAY  SUT13315	LACERATION TRAY  SUT13400	SNAG FREE PLASTICS TRAY W/OR INSTRUMENTS  SUT13510	LACERATION TRAY  SUT13535	PLASTICS SUTURE TRAY  SUT13550	LACERATION TRAY  SUT13555	SUTURE TRAY  SUT13620	LACERATION TRAY  SUT13620	LACERATION

## Reason for recall

Incomplete seals on the sterile package may compromise the sterility

## Distribution

Nationwide  Foreign: GHANA

## Key facts

- **Recall number:** Z-1057-2020
- **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-1057-2020

## Citation

> AI Analytics. FDA recall Z-1057-2020. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1057-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
