# FDA recall Z-1055-2020

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

## Product

Centurion-Pelvic  PE120	LARGE/MEDIUM PELVIC TRAY  PE2200	PELVIC EXAM TRAY  PE2200	PELVIC EXAM TRAY  PE2400	PELVIC EXAM TRAY  PE2515	SMALL GYN EXAM TRAY  PE2515	SMALL GYN EXAM TRAY  PE2610	PELVIC EXAM TRAY  PE2700	ULTRASOUND TRAY  PE2700	ULTRASOUND TRAY  PE2820	VAG/VIRGIN VAG EXAM TRAY  PE2835	PELVIC EXAM TRAY  PE2835	PELVIC EXAM TRAY  PE2905	HSG TRAY  PE2955	7PELVIC EXAM TRAY  PE2965	DISPOSABLE PELVIC EXAM TRAY  PE2965	DISPOSABLE PELVIC EXAM TRAY  PE3125	PELVIC EXAM TRAY  PE3195	PELVIC EXAM TRAY  PE3285	PELVIC EXAM TRAY  PE3360	PELVIC EXAM TRAY W/LIGHT  PE3375	PELVIC EXAM TRAY  PE3400	MEDIUM GYN EXAM TRAY  PE3475	IUD TRAY  PE3585	MEDIUM/LARGE PELVIC EXAM TRAY  PE860	VAGINAL BLEEDER KIT

## Reason for recall

Incomplete seals on the sterile package may compromise the sterility

## Distribution

Nationwide  Foreign: GHANA

## Key facts

- **Recall number:** Z-1055-2020
- **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-1055-2020

## Citation

> AI Analytics. FDA recall Z-1055-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1055-2020. Source: US FDA. Licensed CC0.

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