# FDA recall Z-1119-2023

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2022-12-07.

## Product

Surgical convenience kits labeled as:   a)	CENTURION MEDICAL PRODUCTS CHEST TUBE INSERTION TRAY, Reorder Number CVI2105;   b)	CENTURION MEDICAL PRODUCTS VASECTOMY KIT, Reorder Number MNS11975;   c)	CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT11670;   d)	CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT12060;   e)	CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT14705;   f)	CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT17190;   g)	CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT17195;   h)	CENTURION MEDICAL PRODUCTS LACERATION TRAY (P/S), Reorder Number SUT17755;   i)	CENTURION MEDICAL PRODUCTS LACERATION TRAY (P/S), Reorder Number SUT18475;   j)	CENTURION MEDICAL PRODUCTS SUTURE SET, Reorder Number SUT19505;   k)	CENTURION MEDICAL PRODUCTS LACERATION TRAY, Reorder Number SUT19620;   l)	CENTURION MEDICAL PRODUCTS UNITYPOINT HEALTH LACERATION T, Reorder Number SUT20205;   m)	CENTURION MEDICAL PRODUCTS LACERATION TR

## Reason for recall

The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-1119-2023
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-07
- **Report date:** 2023-02-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1119-2023

## Citation

> AI Analytics. FDA recall Z-1119-2023. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-1119-2023. Source: US FDA. Licensed CC0.

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