# FDA recall Z-2791-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-06-11.

## Product

Medline medical convenience kits labeled as:    1) TOTAL JOINT PACK Medline Kit SKU DYNJ65065A:   2) EXTREMITY/FOOT PACK Medline Kit SKU DYNJ65066B:   3) ANTERIOR CERVICAL-SMH Medline Kit SKU DYNJ907718B:   4) LAMINECTOMY-SMH Medline Kit SKU DYNJ907732C:   5) KYPHOPLASTY Medline Kit SKU DYNJ907984C:   6) LUMBAR LAMINECTOMY Medline Kit SKU DYNJ907987D:   7) KYPHOPLASTY TRAY Medline Kit SKU DYNJ908413C:   8) CRANIOTOMY Medline Kit SKU DYNJ910626:   9) NEURO SPINE Medline Kit SKU DYNJ910639.

## Reason for recall

Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.

## Distribution

US:  CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.

## Key facts

- **Recall number:** Z-2791-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-11
- **Report date:** 2026-07-29

- **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-2791-2026

## Citation

> AI Analytics. FDA recall Z-2791-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/Z-2791-2026. Source: US FDA. Licensed CC0.

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