# FDA recall Z-1095-2020

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

## Product

Centurion-	  P151659	BIOPSY TRAY  P243133	LATEX TUBING PACK  P243133	LATEX TUBING PACK  P243133	LATEX TUBING PACK  P261569	PACK BIOPSY  P392929	BMT-LACERATION PACK  P429589A	TRAY BONE MARRO ASC LTX SAFE  P734457	SUTURE REMOVAL PACK LATEX SAFE  P751651A	BIOPSY PROCEDURE PACK  P758486	PVP PREP PACK  P758486	PVP PREP PACK  P922260	ALCOHOL PREP PACK  P928310	WET PREP TRAY  P928310	WET PREP TRAY  P948416	LACERATION PACK  P966455A	BREAST BIOPSY PACK-LF

## Reason for recall

Incomplete seals on the sterile package may compromise the sterility

## Distribution

Nationwide  Foreign: GHANA

## Key facts

- **Recall number:** Z-1095-2020
- **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-1095-2020

## Citation

> AI Analytics. FDA recall Z-1095-2020. Retrieved 2026-06-22 from https://api.ai-analytics.org/recall/Z-1095-2020. Source: US FDA. Licensed CC0.

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