# FDA recall Z-1883-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-02-27.

## Product

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    BASIC CL PACK-LF	DYNJ87052    BASIC PACK	DYNJ83976  	  BASIC SET UP PACK	DYNJ80700  	  CORONARY ANGIOGRAPHY PACK (N)	DYNJ42136B  	  CSTM ANGIO KIT - S VASC1109  	  CV PACK	DYNJ46301C  	  DR F PACK	DYNJ41253B  	  ENSEMBLE HEMORROIDES	DYNJ56311A  	  G TAVR PACK	DYNJ61006  	  IR MINOR PACK	DYNJ44139C  	  MAJOR PLUS PACK	DYNJ905160N  	  MAXIMUM BARRIER BUNDLE PACK	DYNJ35216C  	  PCI PACK TBRHSC-LF	DYNJ41941D  	  PERC PACK-LF	DYNJ0774759P  	  PERIPHERAL ANGIOGRAPHY PK	DYNJ42094B  	  PROCEDURE PACK	DYNJ55063B  	  PTCA PACK	DYNJ55359B  	  ROBOTIC PACK	DYNJ908706C  	  SPECIAL PROCEDURES TRAY	DYNJ41174A  	  SYRINGE WIRE KIT SANFORD	SAMPC0644  	  WPH EP PACK	DYNJ62745  	  X-RAY PACK	DYNJ44295G

## Reason for recall

Unapproved design changes to the products outside of the 510(k) clearance.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.

## Key facts

- **Recall number:** Z-1883-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-27
- **Report date:** 2026-04-29

- **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-1883-2026

## Citation

> AI Analytics. FDA recall Z-1883-2026. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-1883-2026. Source: US FDA. Licensed CC0.

---

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