# FDA recall Z-0886-2026

> **Medline Industries, LP** · Class II · device recall initiated 2025-10-27.

## Product

MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C

## Reason for recall

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe.

## Distribution

US Nationwide distribution in the state of CA.

## Key facts

- **Recall number:** Z-0886-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-27
- **Report date:** 2025-12-17

- **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-0886-2026

## Citation

> AI Analytics. FDA recall Z-0886-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0886-2026. Source: US FDA. Licensed CC0.

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