# FDA recall Z-1095-2023

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2022-11-17.

## Product

Sterile Procedural Trays, labeled as the following:      a.	BASIC EYE PACK-LF  b.	VITRECTOMY PACK-LF  c.	EYE PACK-EAST-LF  d.	OSC OCULAR PLASTIC PACK-LF  e.	EYE PACK  f.	OCULOPLASTIC PACK  g.	EYE PLASTIC PACK  h.	PLASTIC EYE PACK  i.	DR H BLEPH PACK  j.	BLEPH PACK  k.	OPHTHALMOLOGY PACK  l.	OCULOPLASTIC PACK  m.	BLEPH PACK  n.	EYE PACK  o.	OCULAR PLASTIC PACK  p.	OCULOPLASTIC PACK

## Reason for recall

Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Japan, Mexico, Panama, Turks & Caicos, United Arab Emirates.

## Key facts

- **Recall number:** Z-1095-2023
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-17
- **Report date:** 2023-02-15

- **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-1095-2023

## Citation

> AI Analytics. FDA recall Z-1095-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1095-2023. Source: US FDA. Licensed CC0.

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