# FDA recall Z-2041-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-03-16.

## Product

Medline and Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as:    1. FOLEY CARE KIT, Medline Kit SKU UROT1044;   2. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770;   3. IV START KIT, Medline Kit SKU DYNDV2520;   4. ARTERIAL LINE BUNDLE, Medline Kit SKU ART255;   5. ON/OFF TRAY, Medline Kit SKU DYNDC2969;   6. IV START KIT, Medline Kit SKU DYNDV2520;   7. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770;   8. (Centurion) ARTERIAL LINE BUNDLE, Medline Kit SKU ART255;   9. ON/OFF TRAY, Medline Kit SKU DYNDC2969;   10. CVAD DRESSING CHANGE KIT, Medline Kit SKU EBSI1364A.

## Reason for recall

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2041-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-16
- **Report date:** 2026-05-06

- **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-2041-2026

## Citation

> AI Analytics. FDA recall Z-2041-2026. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-2041-2026. Source: US FDA. Licensed CC0.

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