# FDA recall Z-3070-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-07-20.

## Product

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators    BLOOD CULTURE PINK PERIPHERAL	  	DYNDV1875  	  BOTTOM DRAWER	  	ACC010972  		  DRAWER #4	  	ACC010479A	  	  DRAWER 2	  	ACC010690          ACC010875    DRAWER 3 SYR/DRS/MON/NG 1 OF 3	  	ACC011073  	  DRAWER 4 CIRCULATION	  	ACC011088  	  DRAWER 5 - LEFT BOX	  	ACC011067    LABOR TRIAGE KIT - LF #13232	  	DYKM1564  	  	DYKM1564A  	  LINEN UNIVERSAL PACK	  	DYNJT10325  	  MAC KIT	  	DYKS1089B  	  NICU LINE PACK	  	DYNJ63410  	  PEDIATRIC BLOOD CULTURE KIT	  	DYNDH1363  	  RRMC CODE CART DRAWER 3	  	ACC010770  	    STANFORD TIME TO POSITIVITY	  	DYNDH1591	    STUDENT PRACTICE BAG W LOGO	  	EDUC1043          EDUC1043A    SUTURED SHEATH W/SCI #113198	  	DYKM1496		  	  IV START KIT	  	DYNDV2520

## Reason for recall

Downstream recall - manufacturer recalled specific lots of BD ChloraPrep Clear - 1mL Applicators. Affected product may exhibit an open or incomplete seal on the packaging of the applicator. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3070-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-20
- **Report date:** 2026-09-09

- **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-3070-2026

## Citation

> MORVS. FDA recall Z-3070-2026. Retrieved 2026-10-23 from https://api.morvs.ai/recall/Z-3070-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*