# FDA recall Z-2045-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-05-23.

## Product

Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as:  RETINAL PACK-LF, REF DYNJ0151148B

## Reason for recall

Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow to retract or fails to retract.

## Distribution

US Nationwide distribution in the states of IN, KY, CA, MI, TX, WA.

## Key facts

- **Recall number:** Z-2045-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-23
- **Report date:** 2025-07-09

- **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-2045-2025

## Citation

> AI Analytics. FDA recall Z-2045-2025. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-2045-2025. Source: US FDA. Licensed CC0.

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